Fibroblast growth factor receptor 1: Difference between revisions

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{{Infobox_gene}}
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'''Fibroblast growth factor receptor 1''' ('''FGFR1'''), also known as '''basic fibroblast growth factor receptor 1''', '''fms-related tyrosine kinase-2 / Pfeiffer syndrome''', and [[cluster of differentiation|CD]]331, is a [[receptor tyrosine kinase]] whose ligands are specific members of the [[fibroblast growth factor]] family. FGFR1 has been shown to be associated with [[Pfeiffer syndrome]].<ref name="pmid2162671">{{cite journal | vauthors = Itoh N, Terachi T, Ohta M, Seo MK | title = The complete amino acid sequence of the shorter form of human basic fibroblast growth factor receptor deduced from its cDNA | journal = Biochemical and Biophysical Research Communications | volume = 169 | issue = 2 | pages = 680–5 | date = Jun 1990 | pmid = 2162671 | doi = 10.1016/0006-291X(90)90384-Y }}</ref>
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}


<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
== Gene ==
{{GNF_Protein_box
The ''FGFR1'' gene is located on human chromosome 8 at position p11.23 (i.e. 8p11.23), has 24 exons, and codes for a [[Precursor mRNA]] that is [[RNA splicing|alternatively spliced]] at exons 8A or 8B thereby generating two [[mRNA]]s coding for two FGFR1 [[isoforms]], FGFR1-IIIb (also termed FGFR1b) and FGFR1-IIIc (also termed FGFR1c), respectively. Although these two isoforms have different tissue distributions and FGF-binding affinities, FGFR1-IIIc appears responsible for most of functions of the FGFR1 gene while FGFR1-IIIb appears to have only a minor, somewhat redundant functional role.<ref>https://www.ncbi.nlm.nih.gov/gene/2260</ref><ref name="pmid26277103">{{cite journal | vauthors = Gonçalves C, Bastos M, Pignatelli D, Borges T, Aragüés JM, Fonseca F, Pereira BD, Socorro S, Lemos MC | title = Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform | journal = Fertility and Sterility | volume = 104 | issue = 5 | pages = 1261–7.e1 | year = 2015 | pmid = 26277103 | doi = 10.1016/j.fertnstert.2015.07.1142 | url = }}</ref> There are four other members of the ''FGFR1'' gene family: [[FGFR2]], [[FGFR3]], [[FGFR4]], and [[Fibroblast growth factor receptor-like 1]] (FGFRL1). The ''FGFR1'' gene, similar to the '''FGFR2-4'' genes are commonly activated in human cancers as a result of their [[Gene duplication|duplication]], [[chromosome translocation|fusion with other genes]], and [[point mutation]]; they are therefore classified as [[proto-oncogenes]].<ref name="pmid23696246">{{cite journal | vauthors = Katoh M, Nakagama H | title = FGF receptors: cancer biology and therapeutics | journal = Medicinal Research Reviews | volume = 34 | issue = 2 | pages = 280–300 | year = 2014 | pmid = 23696246 | doi = 10.1002/med.21288 | url = }}</ref>
| image = PBB_Protein_FGFR1_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1agw.
| PDB = {{PDB2|1agw}}, {{PDB2|1cvs}}, {{PDB2|1evt}}, {{PDB2|1fgi}}, {{PDB2|1fgk}}, {{PDB2|1fq9}}, {{PDB2|2ckn}}, {{PDB2|2cr3}}, {{PDB2|2fgi}}
| Name = Fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)
| HGNCid = 3688
| Symbol = FGFR1
| AltSymbols =; BFGFR; CD331; CEK; FGFBR; FLG; FLT2; HBGFR; KAL2; N-SAM
| OMIM = 136350
| ECnumber = 
| Homologene = 69065
| MGIid = 95522
| GeneAtlas_image1 = PBB_GE_FGFR1_211535_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_FGFR1_207937_x_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0004713 |text = protein-tyrosine kinase activity}} {{GNF_GO|id=GO:0004872 |text = receptor activity}} {{GNF_GO|id=GO:0005007 |text = fibroblast growth factor receptor activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0005524 |text = ATP binding}} {{GNF_GO|id=GO:0008201 |text = heparin binding}} {{GNF_GO|id=GO:0016740 |text = transferase activity}}
  | Component = {{GNF_GO|id=GO:0005624 |text = membrane fraction}} {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}}
| Process = {{GNF_GO|id=GO:0000165 |text = MAPKKK cascade}} {{GNF_GO|id=GO:0001501 |text = skeletal development}} {{GNF_GO|id=GO:0001525 |text = angiogenesis}} {{GNF_GO|id=GO:0001759 |text = induction of an organ}} {{GNF_GO|id=GO:0002053 |text = positive regulation of mesenchymal cell proliferation}} {{GNF_GO|id=GO:0006468 |text = protein amino acid phosphorylation}} {{GNF_GO|id=GO:0007420 |text = brain development}} {{GNF_GO|id=GO:0007435 |text = salivary gland morphogenesis}} {{GNF_GO|id=GO:0008543 |text = fibroblast growth factor receptor signaling pathway}} {{GNF_GO|id=GO:0016049 |text = cell growth}} {{GNF_GO|id=GO:0030324 |text = lung development}} {{GNF_GO|id=GO:0030326 |text = embryonic limb morphogenesis}} {{GNF_GO|id=GO:0042472 |text = inner ear morphogenesis}} {{GNF_GO|id=GO:0043066 |text = negative regulation of apoptosis}} {{GNF_GO|id=GO:0048469 |text = cell maturation}} {{GNF_GO|id=GO:0048754 |text = branching morphogenesis of a tube}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 2260
    | Hs_Ensembl = ENSG00000077782
    | Hs_RefseqProtein = NP_056934
    | Hs_RefseqmRNA = NM_015850
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 8
    | Hs_GenLoc_start = 38389406
    | Hs_GenLoc_end = 38445296
    | Hs_Uniprot = P11362
    | Mm_EntrezGene = 14182
    | Mm_Ensembl = ENSMUSG00000031565
    | Mm_RefseqmRNA = NM_001079908
    | Mm_RefseqProtein = NP_001073377
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 8
    | Mm_GenLoc_start = 26997826
    | Mm_GenLoc_end = 27039466
    | Mm_Uniprot = Q3TJ05
  }}
}}


== Protein ==
=== Receptor ===
FGFR1 is a member of the [[fibroblast growth factor receptor]] (FGFR) family, which in addition to FGFR1, includes FGFR2, FGFR3, FGFR4, and FGFRL1. FGFR1-4 are [[Cell surface receptor|cell surface membrane receptors]] that possess [[tyrosine kinase]] activity. A full-length representative of these four receptors consists of an extracellular region composed of three [[immunoglobulin]]-like domains which bind their proper [[Ligand (biochemistry)|ligands]], the [[fibroblast growth factors]] (FGFs), a single hydrophobic stretch which passes through the cell's surface membrane, and a cytoplasmic tyrosine kinase domain. When bonded to FGFs, these receptors form [[Dimer (chemistry)|dimers]] with any one of the four other FGFRs and then [[Protein phosphorylation|cross-phosphorylate]] key [[tyrosine]] residues on their dimer partners. These newyly phosphorylated sites bind cytosolic docking proteins such as [[FRS2]], [[PRKCG]] and [[GRB2]] which proceed to activate [[cell signaling]] pathways that lead to [[cellular differentiation]], growth, proliferation, prolonged survival, migration, and other functions. FGFRL1 lacks a prominent intracellular domain and tyrosine kinase activity; it may serve as a decoy receptor by binding with and thereby diluting the action of FGFs.<ref name="pmid23696246"/><ref name="pmid23880303">{{cite journal | vauthors = Kelleher FC, O'Sullivan H, Smyth E, McDermott R, Viterbo A | title = Fibroblast growth factor receptors, developmental corruption and malignant disease | journal = Carcinogenesis | volume = 34 | issue = 10 | pages = 2198–205 | year = 2013 | pmid = 23880303 | doi = 10.1093/carcin/bgt254 | url = }}</ref> There are 18 known FGRs that bind to and activate one or more of the FGFRs: FGF1 to FGR10 and FGF16 to FGF23. Fourteen of these, FGF1 to FGF6, FGF8, FGF10, FGF17, and FGF19 to FG23 bind and activate FGFR1.<ref name="pmid26224133">{{cite journal | vauthors = Helsten T, Schwaederle M, Kurzrock R | title = Fibroblast growth factor receptor signaling in hereditary and neoplastic disease: biologic and clinical implications | journal = Cancer Metastasis Reviews | volume = 34 | issue = 3 | pages = 479–96 | year = 2015 | pmid = 26224133 | pmc = 4573649 | doi = 10.1007/s10555-015-9579-8 | url = }}</ref> FGFs binding to FGFR1 is promoted by their interaction with cell surface [[Heparan sulfate#proteoglycan|heparan sulfate proteoglycans]] and, with respect to FGF19, FGF20, and FGR23, the [[transmembrane protein]] [[Klotho (biology)|Klotho]].<ref name="pmid26224133"/>


'''Fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)''', also known as '''FGFR1''', is a [[fibroblast growth factor receptor]] associated with [[Pfeiffer syndrome]].
=== Cell activation ===
FGFR1, when bound to a proper FGF, elicits cellular responses by activating signaling pathways that include the: '''a)''' [[Phospholipase C]]/[[PI3K/AKT/mTOR pathway|PI3K/AKT]], '''b)''' [[Ras subfamily]]/[[MAPK/ERK pathway|ERK]], '''c)''' [[Protein kinase C]], '''d)''' [[Inositol trisphosphate|IP3-induced raising of cytosolic Ca<sup>2+</sup>]], and '''e)''' Ca<sup>2+</sup>/[[calmodulin]]-activated elements and pathways. The exact pathways and elements activated depend on the cell type being stimulated plus other factors such as the stimulated cells microenvironment and previous as well as concurrent history of stimulation<ref name="pmid23696246"/><ref name="pmid23880303"/>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
[[File:SH2 domains in complex with FGFR1 kinase.jpg|thumb|right|Figure 1. SH2 domains in complex with FGFR1 kinase. c-SH2 domain is colored in blue, n-SH2 domain is colored in red, and the interdomain linker is colored in yellow. FGFR1 kinase (green) interacts with n-SH2 domain at its C-terminal tail. The structure contains typical SH2 domain, with two α-helices and three antiparallel β-strands on each of the SH2 domains.]]
{{PBB_Summary
| section_title =
| summary_text = The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member binds both acidic and basic fibroblast growth factors and is involved in limb induction. Mutations in this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Chromosomal aberrations involving this gene are associated with stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized.<ref>{{cite web | title = Entrez Gene: FGFR1 fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2260| accessdate = }}</ref>
}}


==See also==
Activation of the gamma isoforms of [[phospholipase C]] (PLCγ) (see [[PLCG1]] and [[PLCG2]] illustrates one mechanism by which FGFR1 activates cell stimulating pathways. Following its binding of a proper FGF and subsequent pairing with another FGFR, FGFR1 becomes [[Tyrosine phosphorylation|phosphorylated]] by its partner FGFR on a highly conserved tyrosine residue (Y766) at its C-terminal. This creates a binding or "docking" site to recruit PLCγ via PLCγ tandem [[SH2 domain|nSH2 and cSH2 domains]] and then phosphorylate PLCγ. By being phosphorylated PLCγ is relieved of its auto-inhibition structure and becomes active in metabolizing nearby [[Phosphatidylinositol 4,5-bisphosphate]] (PIP2) to two [[Second messenger system|secondary messengers]], [[Inositol trisphosphate|inositol 1,4,5-trisphosphate]] (IP3) and [[diacyglycerol]] (DAG). These secondary messengers proceed to mobilize other cell-signaling and cell-activating agents: IP3 elevates cytosolic Ca<sup>2+</sup> and thereby various [[Calcium signaling|Ca<sup>2+</sup>-sensitive]] elements while DAG activates various [[protein kinase C]] isoforms.<ref name="pmid26224133"/>
 
Recent publication on the 2.5 Å crystal structure of PLCγ in complex with FGFR1 kinase (PDB: 3GQI) provides new insights in understanding the molecular mechanism of FGFR1's recruitment of PLCγ by its SH2 domains. Figure 1 on the extreme right shows the PLCγ-FGFR1 kinase complex with the c-SH2 domain colored in red, n-SH2 domain colored in blue, and the interdomain linker colored in yellow. The structure contains typical SH2 domain, with two [[Alpha helix|α-helices]] and three [[Beta sheet#Hydrogen bonding patterns|antiparallel β-strands]] in each SH2 domain. In this complex, the phosphorylated tyrosine (pY766) on the C-terminal tail of FGFR1 kinase binds preferentially to the nSH2 domain of PLCγ. The phosphorylation of tyrosine residue 766 on FGFR1 kinase forms hydrogen bonds with the n-SH2 to stabilize the complex. Hydrogen bonds in the binding pocket help to stabilize the PLCγ-FGFR1 kinase complex. The water molecule as shown mediates the interaction of asparagine 647 (N647) and aspartate 768 (D768) to further increase the binding affinity of the n-SH2 and FGFR1 kinase complex. (Figure 2). The phosphorylation of tyrosine 653 and tyrosine 654 in the active kinase conformation causes a large conformation change in the activation segment of FGFR1 kinase. Threonine 658 is moved by 24Å from the inactive form (Figure 3.) to the activated form of FGFR1 kinase (Figure 4.). The movement causes the closed conformation in the inactive form to open to enable substrate binding. It also allows the open conformation to coordinate Mg2+ with AMP-PCP (analog of ATP). In addition, pY653 and pY654 in the active form helps to maintain the open conformation of the SH2 and FGFR1 kinase complex. However, the mechanism by which the phosphorylation at Y653 and Y654 helps to recruit the SH2 domain to its C-terminal tail upon phosphorylation of Y766 remains elusive. Figure 5 shows the overlay structure of active and inactive forms of FGFR1 kinase. Figure 6 shows the dots and contacts on phosphorylated tyrosine residues 653 and 654. Green dots show highly favorable contacts between pY653 and pY654 with surrounding residues. Red spikes show unfavorable contacts in the activation segment. The figure is generated through Molprobity extension on Pymol.
<gallery mode="packed-hover" height="180">
File:Hydrogen bonds at pY766.jpg|''[[Figure 2. Hydrogen bonds at pY766]]''
File:Closed conformation in Inactive FRFR1 kinase.jpg|''[[Figure 3. Closed conformation in Inactive FRFR1 kinase]]''
File:Open conformation in active FRFR1 kinase.jpg|''[[Figure 4. Open conformation in active FRFR1 kinase]]''
File:Overlay Structures of Active and Inactive Forms of FGFR1 kinase.jpg|''[[Figure 5. Overlay Structures of Active and Inactive Forms of FGFR1 kinase]]''
File:Dots and contacts on pY653 & pY654.jpg|''[[Figure 6. Dots and contacts on pY653 & pY654]]''
File:Β-factor of PLC-FGFR1 kinase.jpg|''[[Figure 7. The β-factor of the PLC-FGFR1 kinase complex]]''
</gallery>
 
[[File:Interface on the N-SH2 binding site and FGFR1 kinase.jpg|thumb|right|Figure 8. Interface on the N-SH2 binding site and FGFR1 kinase. The FGFR1 kinase is bound to the N-SH2 domain primarily through charged amino acids. The acid base pair (D755 and R609) located in the middle of the interface are nearly parallel to each other, indicating a highly favorable interaction.]]
The tyrosine kinase region of FGFR1 binds to the N-SH2 domain of PLCγ primarily through charged amino acids. Arginine residue (R609) on the N-SH2 domain forms a salt bridge to aspartate 755 (D755) on the FGFR1 domain. The acid base pairs located in the middle of the interface are nearly parallel to each other, indicating a highly favorable interaction. The N-SH2 domain makes an additional polar contact through water-mediated interaction that takes place between the N-SH2 domain and the FGFR1 kinase region. Interestingly, the arginine residue 609 (R609) on the FGFR1 kinase also forms a salt bridge to the aspartate residue (D594) on the N-SH2 domain. The acid-base pair interacts with each other carry out a [[redox|reduction–oxidation reaction]] that stabilizes the complex (Figure 7). Previous studies have done to elucidate the binding affinity of the n-SH2 domain with the FGFR1 kinase complex by mutating these phenyalanine or valine amino acids. The results from isothermal titration calorimetry (ITC) indicated that the binding affinity of the complex decreased by 3 to 6-fold, without affecting the phosphorylation of the tyrosine residues.
<ref>{{cite journal | vauthors = Bae JH, Lew, ED, Yuzawa S, Tome F, Lax I, Schlessinger J | title = The Selectivity of Receptor Tyrosine Kinase Signaling Is Controlled by a Secondary SH2 Domain Binding Site | journal = Cell | volume = 138 | issue = 3 | date = Aug 2009 | pmid = 19665973 | doi = 10.1016/j.cell.2009.05.028 | pages=514–24 | pmc=4764080}}</ref>
 
=== Cell inhibition ===
FGF-induced activation of FGFR1 also stimulates the activation of sprouty proteins [[SPRY1]], [[SPRY2]], [[SPRY3]], and/or [[SPRY4]] which in turn interact with GRB2, [[SOS1]], and/or [[c-Raf]] to reduce or inhibit further cell stimulation by activated FGFR1 as well as other tyrosine kinase receptors such as the [[Epidermal growth factor receptor]]. These interactions serve as [[negative feedback loop]]s to limit the extent of cellular activation.<ref name="pmid26224133"/>
 
== Function ==
Mice genetically engineered to lack a functional ''Fgfr1'' gene ([[ortholog]] of the human ''FGFR1'' gene) die in utero before 10.5 days of gestation. Embryos exhibit extensive deficiencies in the development and organization of [[mesoderm]]-derived tissues and the [[musculoskeletal system]]. The ''Fgfr1'' gene appears critical for the [[Somitogenesis|truncation of embryonic structures]] and formation of muscle and bone tissues and thereby the normal formation of limbs, skull, outer, middle, and inner ear, [[neural tube]], tail, and lower spine as well as normal hearing.<ref name="pmid26224133"/><ref name="pmid9169049">{{cite journal | vauthors = Deng C, Bedford M, Li C, Xu X, Yang X, Dunmore J, Leder P | title = Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development | journal = Developmental Biology | volume = 185 | issue = 1 | pages = 42–54 | year = 1997 | pmid = 9169049 | doi = 10.1006/dbio.1997.8553 | url = }}</ref><ref name="pmid21479780">{{cite journal | vauthors = Calvert JA, Dedos SG, Hawker K, Fleming M, Lewis MA, Steel KP | title = A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice | journal = Mammalian Genome | volume = 22 | issue = 5-6 | pages = 290–305 | year = 2011 | pmid = 21479780 | pmc = 3099004 | doi = 10.1007/s00335-011-9324-8 | url = }}</ref>
 
== Clinical significance ==
=== Congenital diseases ===
Hereditary mutations in the ''FGFR1'' gene are associated with various congenital malformations of the [[musculoskeletal system]]. Interstitial deletions at human chromosome 8p12-p11, arginine to a stop [[nonsense mutation]] at FGFR1 amino acid 622 (annotated as R622X), and numerous other [[autosomal dominant]] inactivating mutations in ''FGFR1'' are responsible for ~10% of the cases of [[Kallmann syndrome]]. This syndrome is a form of [[hypogonadotropic hypogonadism]] associated in a varying percentage of cases with [[anosmia]] or [[hyposmia]]; [[cleft palate]] and other craniofacial defects; and [[scoliosis]] and other musculoskeletal malformations. An activating mutation in FGFR1 viz., P232R (proline-to-arginine substitution in the protein's 232nd amino acid), is responsible for the Type 1 or classic form of (Pfeiffer syndrome]], a disease characterized by [[craniosynostosis]] and mid-face deformities. A tyrosine-to-cysteine substitution mutation in the 372nd amino acid pf FGFR1 (Y372C) is responsible for some cases of Osteoglophonic dysplasia. This mutation results in [[craniosynostosis]], mandibular [[prognathism]], [[hypertelorism]], [[brachydactyly]], and inter-phalangeal joint fusion. Other inherited defects associated with '''FGFR1'' mutations likewise involve musculoskeletal malformatios: these include the [[Jackson–Weiss syndrome]] (proline to arg substitution at amino acid 252), [[Antley-Bixler syndrome]] (isoleucine-to-threonine at amino acid 300 (I300T), and [[Trigonocephaly]] (mutation the same as the one for the Antley-Bixler syndrome viz., I300T).<ref name="pmid23880303"/><ref name="pmid26224133"/><ref>https://omim.org/entry/136350#editHistory</ref>
 
=== Cancers ===
 
[[Mutation#Somatic mutations|Somatic mutations]] and [[Cancer epigenetics|epigenetic changes]] in the expression of the ''FGFR1'' gene occur in and are thought to contribute to various types of lung, breast, hematological, and other types of cancers.
 
==== Lung cancers ====
[[Gene duplication|Amplification]] of the ''FGFR1'' gene (four or more copies) is present in 9 to 22% of patients with [[non-small-cell lung carcinoma]] (NSCLC). ''FGFR1'' amplification was highly correlated with a history of tobacco smoking and proved to be the single largest prognostic factor in a cohort of patients suffering this disease. About 1% of patients with other types of lung cancer show amplifications in FGFR1.<ref name="pmid23696246"/><ref name="pmid23880303"/><ref>https://pct.mdanderson.org/genes/fgfr1/show{{full citation needed|date=April 2015}}</ref><ref>{{cite journal | vauthors = Kim HR, Kim DJ, Kang DR, Lee JG, Lim SM, Lee CY, Rha SY, Bae MK, Lee YJ, Kim SH, Ha SJ, Soo RA, Chung KY, Kim JH, Lee JH, Shim HS, Cho BC | title = Fibroblast growth factor receptor 1 gene amplification is associated with poor survival and cigarette smoking dosage in patients with resected squamous cell lung cancer | journal = Journal of Clinical Oncology | volume = 31 | issue = 6 | pages = 731–7 | date = Feb 2013 | pmid = 23182986 | doi = 10.1200/JCO.2012.43.8622 }}</ref>
 
==== Breast cancers ====
Amplification of ''FGFR1'' also occurs in ~10% of [[Hormone receptor positive breast tumor|estrogen receptor positive breast cancers]], particularly of the [[Gene expression profiling in cancer#Clinical application|luminol subtype B]] form of breast cancer. The presence of ''FGFR1'' amplification has been correlated with resistance to [[Breast cancer#Medication|hormone blocking therapy]] and found to be a poor prognostic factor in the disease.<ref name="pmid23696246"/><ref name="pmid23880303"/>
 
==== Hematological cancers ====
In certain rare hematological cancers, the [[Gene fusion|fusion]] of ''FGFR1'' with various other genes due to [[Chromosomal translocation]]s or [[Mutation#Classification of types#By effect on structure|Interstitial deletions]] create genes that encode chimeric FGFR1 [[Fusion protein]]s. These proteins have continuously active FGFR1-derived [[tyrosine kinase]] and thereby continuously stimulated the cell growth and proliferation. These mutations occur in the early stages of [[myeloid]] and/or [[lymphoid]] cell lines and are the cause of or contribute to the development and progression of certain types of [[hematological malignancies]] that have increased numbers of circulating blood [[eosinophils]], increased numbers of [[bone marrow]] eosinophils, and/or the [[Infiltration (medical)|infiltration]] of eosinophils into tissues. These neoplasms were initially regarded as [[eosinophilia]]s, [[hypereosinophilia]]s, [[Myeloid leukemia]]s, [[myeloproliferative neoplasm]]s, [[myeloid sarcoma]]s, [[lymphoid leukemia]]s, or [[lymphoma#Non-Hodgkin lymphomas|non-Hodgkin lymphomas]]. Based on their association with eosinophils, unique genetic mutations, and known or potential sensitivity to [[tyrosine kinase inhibitor]] therapy, they are now being classified together as [[clonal eosinophilia]]s.<ref name="pmid26486351">{{cite journal | vauthors = Gotlib J | title = World Health Organization-defined eosinophilic disorders: 2015 update on diagnosis, risk stratification, and management | journal = American Journal of Hematology | volume = 90 | issue = 11 | pages = 1077–89 | year = 2015 | pmid = 26486351 | doi = 10.1002/ajh.24196 | url = }}</ref> These mutations are described by connecting the chromosome site for the ''FGFR1'' gene, 8p11 (i.e. human chromosome 8's short arm [i.e. p] at position 11) with another gene such as the ''[[MYO18A]]'' whose site is 17q11 (i.e human chromosome 17's long arm [i.e. q] at position 11) to yield the fusion gene annotated as t(8;17)(p11;q11). These ''FGFR1'' mutations along with the chromosomal location of ''FGFR1A''{{'}}s partner gene and the annotation of the fused gene are given in the following table.<ref name="pmid26276769">{{cite journal | vauthors = Vega F, Medeiros LJ, Bueso-Ramos CE, Arboleda P, Miranda RN | title = Hematolymphoid neoplasms associated with rearrangements of PDGFRA, PDGFRB, and FGFR1 | journal = American Journal of Clinical Pathology | volume = 144 | issue = 3 | pages = 377–92 | year = 2015 | pmid = 26276769 | doi = 10.1309/AJCPMORR5Z2IKCEM | url = }}</ref><ref name="pmid28028030">{{cite journal | vauthors = Reiter A, Gotlib J | title = Myeloid neoplasms with eosinophilia | journal = Blood | volume = 129 | issue = 6 | pages = 704–714 | year = 2017 | pmid = 28028030 | doi = 10.1182/blood-2016-10-695973 | url = }}</ref><ref name="pmid28010895">{{cite journal | vauthors = Appiah-Kubi K, Lan T, Wang Y, Qian H, Wu M, Yao X, Wu Y, Chen Y | title = Platelet-derived growth factor receptors (PDGFRs) fusion genes involvement in hematological malignancies | journal = Critical Reviews in Oncology/hematology | volume = 109 | issue = | pages = 20–34 | year = 2017 | pmid = 28010895 | doi = 10.1016/j.critrevonc.2016.11.008 | url = }}</ref>
 
{| class="wikitable"
|-
! Gene !! locus !! notation !!  !! gene !! locus !! notation !!  !! Gene !! locus !! notation !!  !! gene !! locus !!  notation !!  !! gene !! locus !!  notation
|-
| ''[[MYO18A]]'' || 17q11 || t(8;17)(p11;q11)|| || ''[[CPSF6]]'' || 12q15 || t(8;12)(p11;q15) ||  || ''[[Translocated promoter region|TPR]]'' || 1q25 || t(1;8)(q25p11;; ||  || ''[[HERV-K]]'' || 10q13 || t(8;13)(p11-q13) ||  || ''[[FGFR1OP2]]''  || 12p11 || t(8;12)(p11;q12)
|-
| ''[[ZMYM2]]'' || 13q12 || t(8;13)(p11;q12)|| || ''[[CUTL1]] || 7q22 || t(7;8)(q22;p11) ||  || ''[[SQSTM1]]'' || 5q35 || t(5;8)(q35;p11 ||  || ''[[RANBP2]]'' || 2q13 || t(2;8)(q13;p11) ||  || ''[[LRRFIP1]]'' || 2q37 || t(8;2)(p11;q37)
|-
| ''[[CNTRL]]'' || 9q33 || t(8;9)(p11;q33)|| || ''[[FGFR1OP]]'' || 6q27 || t(6;8)(q27;p11) ||  || ''[[BCR (gene)|BCR]]'' || 22q11 || t(8;22)(p11;q11 ||  || ''[[NUP98]] || 11p15 || t(8;11)(p11-p15) ||  || ''[[MYST3]]'' || 8p11.21 || muliple<ref name="pmid20143402">{{cite journal | vauthors = Patnaik MM, Gangat N, Knudson RA, Keefe JG, Hanson CA, Pardanani A, Ketterling RP, Tefferi A | title = Chromosome 8p11.2 translocations: prevalence, FISH analysis for FGFR1 and MYST3, and clinicopathologic correlates in a consecutive cohort of 13 cases from a single institution | journal = American Journal of Hematology | volume = 85 | issue = 4 | pages = 238–42 | year = 2010 | pmid = 20143402 | doi = 10.1002/ajh.21631 | url = }}</ref>
|-
| ''[[CEP110]]'' || 16p12 || t(8;16)(p11;p12)||
 
|}
 
These cancers are sometimes termed '''8p11 [[Myeloproliferative neoplasm|myeloproliferative syndromes]]''' based on the chromosomal location of the ''FGFR1'' gene. Translocations involving ''ZYMM2'', ''CTRL'', and GFGR10P2 are the most common forms of these 8p11 syndromes.  In general, patients with any of these diseases have an average age of 44 and present with fatigue, [[night sweats]], weight loss, fever, [[lymphadenopathy]], and enlarged liver and/or spleen. They typically evidence hematological features of the [[myeloproliferative syndrome]] with moderate to greatly elevated levels of blood and bone marrow eosinophils. However, patients bearing: '''a)'''  ''ZMYM2-FGFR1'' fusion genes often present as [[T-cell lymphoma]]s with spreading to non-lymphoid tissue; '''b)''' ''FPFR1-BCR'' fusion genes usually present as [[chronic myelogenous leukemia]]s; '''c)''' ''CEP110'' fusion genes may present as a [[chronic myelomonocytic leukemia]] with involvement of tonsil; and '''d)''' ''FPFR1-BCR'' or ''FGFR1-MYST3'' fusion genes often present with little or no eosinophilia. Diagnosis requires conventional [[cytogenetics]] using [[Fluorescence in situ hybridization#Variations on probes and analysis with break-apart probes]] for ''FGFR1''.<ref name="pmid28028030"/><ref name="pmid20143402"/>
 
Unlike many other myeloid neoplasms with eosinophil such as those caused by [[PDGFRA#Myeloid and lymphoid cells|Platelet-derived growth factor receptor A]] or [[PDGFRB#Other PDGFRB translocations|platelet-derived growth factor receptor B]] fusion genes, the myelodysplasia syndromes caused by ''FGFR''1 fusion genes in general do not respond to [[tyrosine kinase inhibitor]]s, are aggressive and rapidly progressive, and require treatment with [[chemotherapy]] agents followed by [[bone marrow transplantion]] in order to improve survival.<ref name="pmid28028030"/><ref name="pmid26276769"/> The tyrosine kinase inhibitor [[Ponatinib]] has been used as mono-therapy and subsequently used in combination with intensive chemotherapy to treat the myelodysplasia caused by the ''FGFR1-BCR'' fusion gene.<ref name="pmid28028030"/>
 
==== Phosphaturic mesenchymal tumor ====
[[Phosphaturic mesenchymal tumor]]s is characterized by a hypervascular proliferation of apparently non-malignant spindled cells associated with a variable amount of ‘smudgy’ calcified matrix but a small subset of these tumors exhibit malignant histological features and may behave in a clinically malignant fashion. In a series of 15 patients with this disease, 9 were found to have tumors that bore fusions between the ''FGFR1'' gene and the [[FN1]] gene located on human chromosome 2 at position q35.<ref name="pmid25319834">{{cite journal | vauthors = Lee JC, Jeng YM, Su SY, Wu CT, Tsai KS, Lee CH, Lin CY, Carter JM, Huang JW, Chen SH, Shih SR, Mariño-Enríquez A, Chen CC, Folpe AL, Chang YL, Liang CW | title = Identification of a novel FN1-FGFR1 genetic fusion as a frequent event in phosphaturic mesenchymal tumour | journal = The Journal of Pathology | volume = 235 | issue = 4 | pages = 539–45 | year = 2015 | pmid = 25319834 | doi = 10.1002/path.4465 | url = }}</ref> The ''FGFR1-FN1'' fusion gene was again identified in 16 of 39 (41%) patients with phosphaturic mesenchymal tumors.<ref name="pmid27443518">{{cite journal | vauthors = Lee JC, Su SY, Changou CA, Yang RS, Tsai KS, Collins MT, Orwoll ES, Lin CY, Chen SH, Shih SR, Lee CH, Oda Y, Billings SD, Li CF, Nielsen GP, Konishi E, Petersson F, Carpenter TO, Sittampalam K, Huang HY, Folpe AL | title = Characterization of FN1-FGFR1 and novel FN1-FGF1 fusion genes in a large series of phosphaturic mesenchymal tumors | journal = Modern Pathology | volume = 29 | issue = 11 | pages = 1335–1346 | year = 2016 | pmid = 27443518 | doi = 10.1038/modpathol.2016.137 | url = }}</ref> The role of the(2;8)(35;11) ''FGFR1-FN1'' fusion gene in this disease is not known.
 
==== Rhabdomyosarcoma ====
Elevated expression of FGFR1 protein was detected in 10 of 10 human [[Rhabdomyosarcoma]] tumors and 4 of 4 human cell lines derived from rhabdomyocarcoma. The tumor cases included 6 cases of [[Alveolar rhabdomyosarcoma]], 2 cases of [[Embryonal rhabdomyosarcoma]], and 2 cases of [[Rhabdomyosarcoma#Types|pleomorphic rhabdomyosarcoma]]. Rhabdomyosarcoma is a highly malignant form of cancer that develops from immature skeletal muscle cell precursors viz., [[myoblasts]]s that have failed to fully [[Cellular differentiation|differentiate]]. FGFR1 activation causes myoblast to proliferate while inhibiting their differentiation, dual effects that may lead to the assumption of a malignant [[phenotype]] by these cells. The 10 human rhabdomyosarcoma tumor exhibited decreased levels of methylation of [[CpG islands]] [[Upstream and downstream (DNA)|upstream]] of the first FGFR1 [[exon]]. CpG islands commonly function to silence expression of adjacent genes while their [[CpG island#Methylation of CpG islands stably silences genes|methylation]] inhibits this silencing. Hypomethylation of CpG islands upstream of FGFR1 is hypothesized to be at least in part responsible for the over-expression of FGFR1 by and malignant behavior of these rhabdomyosarcoma tumors.<ref name="pmid17696196">{{cite journal | vauthors = Goldstein M, Meller I, Orr-Urtreger A | title = FGFR1 over-expression in primary rhabdomyosarcoma tumors is associated with hypomethylation of a 5' CpG island and abnormal expression of the AKT1, NOG, and BMP4 genes | journal = Genes, Chromosomes & Cancer | volume = 46 | issue = 11 | pages = 1028–38 | year = 2007 | pmid = 17696196 | doi = 10.1002/gcc.20489 | url = }}</ref> In addition, a single case of rabdomyosarcoma tumor was found express co-amplified ''FOXO1'' gene at 13q14 and ''FGFR1'' gene at 8p11, i.e. t(8;13)(p11;q14), suggesting the formation, amplification, and malignant activity of a chimerical '''FOXO1-FGFR1''' fusion gene by this tumor.<ref name="pmid23696246"/><ref name="pmid21666686">{{cite journal | vauthors = Liu J, Guzman MA, Pezanowski D, Patel D, Hauptman J, Keisling M, Hou SJ, Papenhausen PR, Pascasio JM, Punnett HH, Halligan GE, de Chadarévian JP | title = FOXO1-FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma | journal = Modern Pathology | volume = 24 | issue = 10 | pages = 1327–35 | year = 2011 | pmid = 21666686 | doi = 10.1038/modpathol.2011.98 | url = }}</ref>
 
==== Other types of cancers ====
Acquired abnormalities if the ''FGFR1'' gene are found in: ~14% of urinary bladder [[Transitional cell carcinoma]]s (almost all are amplifications); ~10% of squamous cell [[Head and neck cancer]]s (~80% amplifications, 20% other mutations); ~7% of [[endometrial cancer]]s (half amplifications, half other types of mutations); ~6% of [[prostate cancer]]s (half amplifications, half other mutations); ~5% of ovarian [[Papillary serous cystadenocarcinoma]] (almost all amplifications); ~5% of [[colorectal cancer]]s (~60 amplifications, 40% other mutations); ~4% of [[sarcoma]]s (mostly amplifications); <3% of [[Glioblastomas]] (Fusion of ''FGFR1''  and ''[[TACC1]]'' (8p11) genes; <3% of [[Salivary gland cancer]] (all amplifications); and <2% in certain other cancers.<ref name="pmid26224133"/><ref name="pmid22837387">{{cite journal | vauthors = Singh D, Chan JM, Zoppoli P, Niola F, Sullivan R, Castano A, Liu EM, Reichel J, Porrati P, Pellegatta S, Qiu K, Gao Z, Ceccarelli M, Riccardi R, Brat DJ, Guha A, Aldape K, Golfinos JG, Zagzag D, Mikkelsen T, Finocchiaro G, Lasorella A, Rabadan R, Iavarone A | title = Transforming fusions of FGFR and TACC genes in human glioblastoma | journal = Science | volume = 337 | issue = 6099 | pages = 1231–5 | year = 2012 | pmid = 22837387 | pmc = 3677224 | doi = 10.1126/science.1220834 | url = }}</ref><ref name="pmid26661925">{{cite journal | vauthors = Ach T, Schwarz-Furlan S, Ach S, Agaimy A, Gerken M, Rohrmeier C, Zenk J, Iro H, Brockhoff G, Ettl T | title = Genomic aberrations of MDM2, MDM4, FGFR1 and FGFR3 are associated with poor outcome in patients with salivary gland cancer | journal = Journal of Oral Pathology & Medicine | volume = 45 | issue = 7 | pages = 500–9 | year = 2016 | pmid = 26661925 | doi = 10.1111/jop.12394 | url = }}</ref>
 
=== FGFR inhibitors ===
 
Recent advances in our knowledge of the FGFR1 system has resulted in attempts to discover therapeutic touch points in the pathway for use in drug development. FGFR-targeted drugs exert direct as well as indirect anticancer effects, because FGFRs on cancer cells and endothelial cells are involved in tumorigenesis and vasculogenesis, respectively.<ref name = "Katoh_2014" >{{cite journal | vauthors = Katoh M, Nakagama H | title = FGF receptors: cancer biology and therapeutics | journal = Medicinal Research Reviews | volume = 34 | issue = 2 | date = Mar 2014 | pmid = 23696246 | doi = 10.1002/med.21288 | pages=280–300}}</ref> FGFR therapeutics are active as FGF affects numerous morphologies of cancers such as invasiveness, stemness and cellular survival. Primary among such drugs are antagonists. Small molecules that fit between the ATP binding pockets of the tyrosine kinase domains of the receptors. For FGFR1 numerous such small molecules are already approved for targeting of the structure of TKI ATP pocket. These include [[dovitinib]] and [[brivanib]]. The table below provides the IC50 (nanomolar) of small-molecule compounds targeting FGFRs.<ref name = "Katoh_2014" />
 
{| class="wikitable"
|-
! [[PD173074]] !! [[Dovitinib]] !! [[Ki23057]] !! [[Lenvatinib]] !! [[Brivanib]] !! [[Nintedanib]] !! [[Ponatinib]] !! [[MK-2461]] !! [[Lucitanib]] !! [[AZD4547]]
|-
| 26|| 8|| NA|| 46|| 148|| 69|| 2.2|| 65 || 18|| 0.2
|}
 
FGFR1 aberration in breast and lung cancer as a result of genetic over-amplification is effectively targeted using dovitinib and [[povatinib]] respectively.<ref name=Fabrice2013>{{cite journal | vauthors = André F, Bachelot T, Campone M, Dalenc F, Perez-Garcia JM, Hurvitz SA, Turner N, Rugo H, Smith JW, Deudon S, Shi M, Zhang Y, Kay A, Porta DG, Yovine A, Baselga J | display-authors = 6 | title = Targeting FGFR with dovitinib (TKI258): preclinical and clinical data in breast cancer | journal = Clinical Cancer Research | volume = 19 | issue = 13 | pages = 3693–702 | year = 2013 | pmid = 23658459 | doi = 10.1158/1078-0432.CCR-13-0190 | url = }}</ref> Drug resistance is a highly relevant topic in the field of drug development for FGFR targets. FGFR inhibitors allow for the increase of tumor sensitivity to regular anticancer drug such as paclitaxel, and etoposide in human cancer cells and thereby enhancing antiapoptotic potential based on aberrant FGFR activation.<ref name = "Katoh_2014"/> Moreover, FGF signaling inhibition dramatically reduces revascularization, hitting upon one of the hallmarks of cancers, angiogenesis, and reduces tumor burden in human tumors that depend on autocrine FGF signaling based on FGF2 upregulation following the common VEGFR-2 therapy for breast cancer. In such a way, FGFR1 can act synergistically with therapies to cut off cancer clonal resurgence by eliminating potential pathways of future relapse.{{citation needed|date=July 2016}}
 
In addition, FGFR inhibitors are predicted to be effective on relapsed tumors because of the clonal evolution of an FGFR-activated minor subpopulation after therapy targeted to EGFRs or VEGFRs. Because there are multiple mechanisms of action for FGFR inhibitors to overcome drug resistance in human cancer, FGFR-targeted therapy is a promising strategy for the treatment of refractory cancer.{{Citation needed|date=May 2015}}
 
[[AZD4547]] has undergone a phase II clinical trial (re gastric cancer) and reported some results.<ref>[http://meetinglibrary.asco.org/content/147853-156 A randomized, open-label phase II study of AZD4547 (AZD) versus Paclitaxel (P) in previously treated patients with advanced gastric cancer (AGC) with Fibroblast Growth Factor Receptor 2 (FGFR2) polysomy or gene amplification (amp): SHINE study.]</ref>
 
[[Lucitanib]] is an inhibitor of [[FGFR1]] and [[FGFR2]] and has undergone clinical trials for advanced solid tumors.<ref name=Soria2014>{{cite journal |pmid=25193991 |title=Phase I/IIa study evaluating the safety, efficacy, pharmacokinetics, and pharmacodynamics of lucitanib in advanced solid tumors. |doi=10.1093/annonc/mdu390 |author=Soria et al. |year=2014 |volume=25 |journal=Ann. Oncol. |pages=2244–51}}</ref>
 
[[Dovitinib]] (TKI258), an inhibitor of FGFR1, [[FGFR2]], and [[FGFR3]], has had a clinical trial on FGFR-amplified breast cancers.<ref>{{cite journal | pmid = 23658459 | doi=10.1158/1078-0432.CCR-13-0190 | volume=19 | title=Targeting FGFR with dovitinib (TKI258): preclinical and clinical data in breast cancer | year=2013 | journal=Clin. Cancer Res. | pages=3693–702 | vauthors=André F, Bachelot T, Campone M, Dalenc F, Perez-Garcia JM, Hurvitz SA, Turner N, Rugo H, Smith JW, Deudon S, Shi M, Zhang Y, Kay A, Porta DG, Yovine A, Baselga J}}</ref>
 
== Interactions ==
Fibroblast growth factor receptor 1 has been shown to [[Protein-protein interaction|interact]] with:
* [[FGF1]],<ref name = "pmid11030354">{{cite journal | vauthors = Schlessinger J, Plotnikov AN, Ibrahimi OA, Eliseenkova AV, Yeh BK, Yayon A, Linhardt RJ, Mohammadi M | date = Sep 2000 | title = Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization | journal = Mol. Cell | volume = 6 | issue = 3 | pages = 743–50 | pmid = 11030354 | doi = 10.1016/s1097-2765(00)00073-3}}</ref><ref name = "pmid8576175">{{cite journal | vauthors = Santos-Ocampo S, Colvin JS, Chellaiah A, Ornitz DM | date = Jan 1996 | title = Expression and biological activity of mouse fibroblast growth factor-9 | journal = J. Biol. Chem. | volume = 271 | issue = 3 | pages = 1726–31 | pmid = 8576175 | doi = 10.1074/jbc.271.3.1726}}</ref>
* [[FRS2]],<ref name = "pmid11877385">{{cite journal | vauthors = Yan KS, Kuti M, Yan S, Mujtaba S, Farooq A, Goldfarb MP, Zhou MM | date = May 2002 | title = FRS2 PTB domain conformation regulates interactions with divergent neurotrophic receptors | journal = J. Biol. Chem. | volume = 277 | issue = 19 | pages = 17088–94 | pmid = 11877385 | doi = 10.1074/jbc.M107963200}}</ref><ref name = "pmid10629055">{{cite journal | vauthors = Ong SH, Guy GR, Hadari YR, Laks S, Gotoh N, Schlessinger J, Lax I | date = Feb 2000 | title = FRS2 proteins recruit intracellular signaling pathways by binding to diverse targets on fibroblast growth factor and nerve growth factor receptors | journal = Mol. Cell. Biol. | volume = 20 | issue = 3 | pages = 979–89 | pmid = 10629055 | pmc = 85215 | doi = 10.1128/mcb.20.3.979-989.2000}}</ref><ref name = "pmid9660748">{{cite journal | vauthors = Xu H, Lee KW, Goldfarb M | date = Jul 1998 | title = Novel recognition motif on fibroblast growth factor receptor mediates direct association and activation of SNT adapter proteins | journal = J. Biol. Chem. | volume = 273 | issue = 29 | pages = 17987–90 | pmid = 9660748 | doi = 10.1074/jbc.273.29.17987 }}</ref><ref name = "pmid11090629">{{cite journal | vauthors = Dhalluin C, Yan KS, Plotnikova O, Lee KW, Zeng L, Kuti M, Mujtaba S, Goldfarb MP, Zhou MM | date = Oct 2000 | title = Structural basis of SNT PTB domain interactions with distinct neurotrophic receptors | journal = Mol. Cell | volume = 6 | issue = 4 | pages = 921–9 | pmid = 11090629 | doi = 10.1016/S1097-2765(05)00087-0 }}</ref>
* [[Klotho (biology)|Klotho]],<ref name = "pmid17086194 ">{{cite journal | vauthors = Urakawa I, Yamazaki Y, Shimada T, Iijima K, Hasegawa H, Okawa K, Fujita T, Fukumoto S, Yamashita T | date = Dec 2006  | title = Klotho converts canonical FGF receptor into a specific receptor for FGF23 | journal = Nature | volume = 444 | issue = 7120 | pages = 770–4 | pmid = 17086194 | doi = 10.1038/nature05315|bibcode = 2006Natur.444..770U }}</ref>
* [[GRB14]],<ref name = "pmid10713090">{{cite journal | vauthors = Reilly JF, Mickey G, Maher PA | date = Mar 2000 | title = Association of fibroblast growth factor receptor 1 with the adaptor protein Grb14. Characterization of a new receptor binding partner | journal = J. Biol. Chem. | volume = 275 | issue = 11 | pages = 7771–8 | pmid = 10713090 | doi = 10.1074/jbc.275.11.7771 }}</ref>  and
* [[SHB (gene)|SHB]].<ref name = "pmid7537362">{{cite journal | vauthors = Karlsson T, Songyang Z, Landgren E, Lavergne C, Di Fiore PP, Anafi M, Pawson T, Cantley LC, Claesson-Welsh L, Welsh M | date = Apr 1995 | title = Molecular interactions of the Src homology 2 domain protein Shb with phosphotyrosine residues, tyrosine kinase receptors and Src homology 3 domain proteins | journal = Oncogene | volume = 10 | issue = 8 | pages = 1475–83 | pmid = 7537362 | doi = }}</ref>
 
== See also ==
* [[Cluster of differentiation]]
* [[Cluster of differentiation]]


==References==
== References ==
{{reflist|2}}
{{reflist|33em}}


==Further reading==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Weiss J, Sos ML, Seidel D, Peifer M, Zander T, Heuckmann JM, Ullrich RT, Menon R, Maier S, Soltermann A, Moch H, Wagener P, Fischer F, Heynck S, Koker M, Schöttle J, Leenders F, Gabler F, Dabow I, Querings S, Heukamp LC, Balke-Want H, Ansén S, Rauh D, Baessmann I, Altmüller J, Wainer Z, Conron M, Wright G, Russell P, Solomon B, Brambilla E, Brambilla C, Lorimier P, Sollberg S, Brustugun OT, Engel-Riedel W, Ludwig C, Petersen I, Sänger J, Clement J, Groen H, Timens W, Sietsma H, Thunnissen E, Smit E, Heideman D, Cappuzzo F, Ligorio C, Damiani S, Hallek M, Beroukhim R, Pao W, Klebl B, Baumann M, Buettner R, Ernestus K, Stoelben E, Wolf J, Nürnberg P, Perner S, Thomas RK | display-authors = 6 | title = Frequent and focal FGFR1 amplification associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer | journal = Science Translational Medicine | volume = 2 | issue = 62 | pages = 62ra93 | date = Dec 2010 | pmid = 21160078 | pmc = 3990281 | doi = 10.1126/scitranslmed.3001451 }}
| citations =
*{{cite book |doi=10.1016/S0065-230X(08)60821-0 |pmid=8417497 |chapter=Structural and Functional Diversity in the FGf Receptor Multigene Family |volume=60 |pages=1–41 |title=Advances in Cancer Research |year=1992 |last1=Johnson |first1=Daniel E. |last2=Williams |first2=Lewis T. | name-list-format = vanc | isbn=978-0-12-006660-5 }}
*{{cite journal | author=Johnson DE, Williams LT |title=Structural and functional diversity in the FGF receptor multigene family. |journal=Adv. Cancer Res. |volume=60 |issue= |pages= 1-41 |year= 1993 |pmid= 8417497 |doi= }}
* {{cite journal | vauthors = Macdonald D, Reiter A, Cross NC | title = The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1 | journal = Acta Haematologica | volume = 107 | issue = 2 | pages = 101–7 | year = 2002 | pmid = 11919391 | doi = 10.1159/000046639 }}
*{{cite journal | author=Macdonald D, Reiter A, Cross NC |title=The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. |journal=Acta Haematol. |volume=107 |issue= 2 |pages= 101-7 |year= 2002 |pmid= 11919391 |doi= }}
* {{cite journal | vauthors = Groth C, Lardelli M | title = The structure and function of vertebrate fibroblast growth factor receptor 1 | journal = The International Journal of Developmental Biology | volume = 46 | issue = 4 | pages = 393–400 | year = 2002 | pmid = 12141425 }}
*{{cite journal | author=Groth C, Lardelli M |title=The structure and function of vertebrate fibroblast growth factor receptor 1. |journal=Int. J. Dev. Biol. |volume=46 |issue= 4 |pages= 393-400 |year= 2003 |pmid= 12141425 |doi=  }}
* {{cite journal | vauthors = Wilkie AO | title = Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations | journal = Cytokine & Growth Factor Reviews | volume = 16 | issue = 2 | pages = 187–203 | date = Apr 2005 | pmid = 15863034 | doi = 10.1016/j.cytogfr.2005.03.001 }}
*{{cite journal | author=Wilkie AO |title=Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations. |journal=Cytokine Growth Factor Rev. |volume=16 |issue= 2 |pages= 187-203 |year= 2005 |pmid= 15863034 |doi= 10.1016/j.cytogfr.2005.03.001 }}
}}
{{refend}}
{{refend}}


==External links==
== External links ==
* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=craniosynostosis GeneReviews/NIH/NCBI/UW entry on FGFR-Related Craniosynostosis Syndromes]
*[https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=kms GeneReviews/NCBI/NIH/UW entry on Kallmann syndrome]
* {{MeshName|FGFR1+protein,+human}}
* {{MeshName|FGFR1+protein,+human}}
* [http://atlasgeneticsoncology.org/Genes/FGFR1113.html Fibroblast growth factor receptor 1] on the [[Atlas of Genetics and Cytogenetics in Oncology and Haematology|Atlas of Genetics and Oncology]]
* {{UCSC genome browser|FGFR1}}
* {{UCSC gene details|FGFR1}}


{{membrane-protein-stub}}
{{NLM content}}
{{NLM content}}
{{PDB Gallery|geneid=2260}}
{{Clusters of differentiation}}
{{Clusters of differentiation}}
[[Category:Clusters of differentiation|*]]
{{Tyrosine kinases}}
{{Receptor tyrosine kinases}}
{{Enzymes}}
{{WikiDoc Sources}}
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[[Category:Clusters of differentiation]]
[[Category:Tyrosine kinase receptors]]

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Fibroblast growth factor receptor 1 (FGFR1), also known as basic fibroblast growth factor receptor 1, fms-related tyrosine kinase-2 / Pfeiffer syndrome, and CD331, is a receptor tyrosine kinase whose ligands are specific members of the fibroblast growth factor family. FGFR1 has been shown to be associated with Pfeiffer syndrome.[1]

Gene

The FGFR1 gene is located on human chromosome 8 at position p11.23 (i.e. 8p11.23), has 24 exons, and codes for a Precursor mRNA that is alternatively spliced at exons 8A or 8B thereby generating two mRNAs coding for two FGFR1 isoforms, FGFR1-IIIb (also termed FGFR1b) and FGFR1-IIIc (also termed FGFR1c), respectively. Although these two isoforms have different tissue distributions and FGF-binding affinities, FGFR1-IIIc appears responsible for most of functions of the FGFR1 gene while FGFR1-IIIb appears to have only a minor, somewhat redundant functional role.[2][3] There are four other members of the FGFR1 gene family: FGFR2, FGFR3, FGFR4, and Fibroblast growth factor receptor-like 1 (FGFRL1). The FGFR1 gene, similar to the 'FGFR2-4 genes are commonly activated in human cancers as a result of their duplication, fusion with other genes, and point mutation; they are therefore classified as proto-oncogenes.[4]

Protein

Receptor

FGFR1 is a member of the fibroblast growth factor receptor (FGFR) family, which in addition to FGFR1, includes FGFR2, FGFR3, FGFR4, and FGFRL1. FGFR1-4 are cell surface membrane receptors that possess tyrosine kinase activity. A full-length representative of these four receptors consists of an extracellular region composed of three immunoglobulin-like domains which bind their proper ligands, the fibroblast growth factors (FGFs), a single hydrophobic stretch which passes through the cell's surface membrane, and a cytoplasmic tyrosine kinase domain. When bonded to FGFs, these receptors form dimers with any one of the four other FGFRs and then cross-phosphorylate key tyrosine residues on their dimer partners. These newyly phosphorylated sites bind cytosolic docking proteins such as FRS2, PRKCG and GRB2 which proceed to activate cell signaling pathways that lead to cellular differentiation, growth, proliferation, prolonged survival, migration, and other functions. FGFRL1 lacks a prominent intracellular domain and tyrosine kinase activity; it may serve as a decoy receptor by binding with and thereby diluting the action of FGFs.[4][5] There are 18 known FGRs that bind to and activate one or more of the FGFRs: FGF1 to FGR10 and FGF16 to FGF23. Fourteen of these, FGF1 to FGF6, FGF8, FGF10, FGF17, and FGF19 to FG23 bind and activate FGFR1.[6] FGFs binding to FGFR1 is promoted by their interaction with cell surface heparan sulfate proteoglycans and, with respect to FGF19, FGF20, and FGR23, the transmembrane protein Klotho.[6]

Cell activation

FGFR1, when bound to a proper FGF, elicits cellular responses by activating signaling pathways that include the: a) Phospholipase C/PI3K/AKT, b) Ras subfamily/ERK, c) Protein kinase C, d) IP3-induced raising of cytosolic Ca2+, and e) Ca2+/calmodulin-activated elements and pathways. The exact pathways and elements activated depend on the cell type being stimulated plus other factors such as the stimulated cells microenvironment and previous as well as concurrent history of stimulation[4][5]

File:SH2 domains in complex with FGFR1 kinase.jpg
Figure 1. SH2 domains in complex with FGFR1 kinase. c-SH2 domain is colored in blue, n-SH2 domain is colored in red, and the interdomain linker is colored in yellow. FGFR1 kinase (green) interacts with n-SH2 domain at its C-terminal tail. The structure contains typical SH2 domain, with two α-helices and three antiparallel β-strands on each of the SH2 domains.

Activation of the gamma isoforms of phospholipase C (PLCγ) (see PLCG1 and PLCG2 illustrates one mechanism by which FGFR1 activates cell stimulating pathways. Following its binding of a proper FGF and subsequent pairing with another FGFR, FGFR1 becomes phosphorylated by its partner FGFR on a highly conserved tyrosine residue (Y766) at its C-terminal. This creates a binding or "docking" site to recruit PLCγ via PLCγ tandem nSH2 and cSH2 domains and then phosphorylate PLCγ. By being phosphorylated PLCγ is relieved of its auto-inhibition structure and becomes active in metabolizing nearby Phosphatidylinositol 4,5-bisphosphate (PIP2) to two secondary messengers, inositol 1,4,5-trisphosphate (IP3) and diacyglycerol (DAG). These secondary messengers proceed to mobilize other cell-signaling and cell-activating agents: IP3 elevates cytosolic Ca2+ and thereby various Ca2+-sensitive elements while DAG activates various protein kinase C isoforms.[6]

Recent publication on the 2.5 Å crystal structure of PLCγ in complex with FGFR1 kinase (PDB: 3GQI) provides new insights in understanding the molecular mechanism of FGFR1's recruitment of PLCγ by its SH2 domains. Figure 1 on the extreme right shows the PLCγ-FGFR1 kinase complex with the c-SH2 domain colored in red, n-SH2 domain colored in blue, and the interdomain linker colored in yellow. The structure contains typical SH2 domain, with two α-helices and three antiparallel β-strands in each SH2 domain. In this complex, the phosphorylated tyrosine (pY766) on the C-terminal tail of FGFR1 kinase binds preferentially to the nSH2 domain of PLCγ. The phosphorylation of tyrosine residue 766 on FGFR1 kinase forms hydrogen bonds with the n-SH2 to stabilize the complex. Hydrogen bonds in the binding pocket help to stabilize the PLCγ-FGFR1 kinase complex. The water molecule as shown mediates the interaction of asparagine 647 (N647) and aspartate 768 (D768) to further increase the binding affinity of the n-SH2 and FGFR1 kinase complex. (Figure 2). The phosphorylation of tyrosine 653 and tyrosine 654 in the active kinase conformation causes a large conformation change in the activation segment of FGFR1 kinase. Threonine 658 is moved by 24Å from the inactive form (Figure 3.) to the activated form of FGFR1 kinase (Figure 4.). The movement causes the closed conformation in the inactive form to open to enable substrate binding. It also allows the open conformation to coordinate Mg2+ with AMP-PCP (analog of ATP). In addition, pY653 and pY654 in the active form helps to maintain the open conformation of the SH2 and FGFR1 kinase complex. However, the mechanism by which the phosphorylation at Y653 and Y654 helps to recruit the SH2 domain to its C-terminal tail upon phosphorylation of Y766 remains elusive. Figure 5 shows the overlay structure of active and inactive forms of FGFR1 kinase. Figure 6 shows the dots and contacts on phosphorylated tyrosine residues 653 and 654. Green dots show highly favorable contacts between pY653 and pY654 with surrounding residues. Red spikes show unfavorable contacts in the activation segment. The figure is generated through Molprobity extension on Pymol.

File:Interface on the N-SH2 binding site and FGFR1 kinase.jpg
Figure 8. Interface on the N-SH2 binding site and FGFR1 kinase. The FGFR1 kinase is bound to the N-SH2 domain primarily through charged amino acids. The acid base pair (D755 and R609) located in the middle of the interface are nearly parallel to each other, indicating a highly favorable interaction.

The tyrosine kinase region of FGFR1 binds to the N-SH2 domain of PLCγ primarily through charged amino acids. Arginine residue (R609) on the N-SH2 domain forms a salt bridge to aspartate 755 (D755) on the FGFR1 domain. The acid base pairs located in the middle of the interface are nearly parallel to each other, indicating a highly favorable interaction. The N-SH2 domain makes an additional polar contact through water-mediated interaction that takes place between the N-SH2 domain and the FGFR1 kinase region. Interestingly, the arginine residue 609 (R609) on the FGFR1 kinase also forms a salt bridge to the aspartate residue (D594) on the N-SH2 domain. The acid-base pair interacts with each other carry out a reduction–oxidation reaction that stabilizes the complex (Figure 7). Previous studies have done to elucidate the binding affinity of the n-SH2 domain with the FGFR1 kinase complex by mutating these phenyalanine or valine amino acids. The results from isothermal titration calorimetry (ITC) indicated that the binding affinity of the complex decreased by 3 to 6-fold, without affecting the phosphorylation of the tyrosine residues. [7]

Cell inhibition

FGF-induced activation of FGFR1 also stimulates the activation of sprouty proteins SPRY1, SPRY2, SPRY3, and/or SPRY4 which in turn interact with GRB2, SOS1, and/or c-Raf to reduce or inhibit further cell stimulation by activated FGFR1 as well as other tyrosine kinase receptors such as the Epidermal growth factor receptor. These interactions serve as negative feedback loops to limit the extent of cellular activation.[6]

Function

Mice genetically engineered to lack a functional Fgfr1 gene (ortholog of the human FGFR1 gene) die in utero before 10.5 days of gestation. Embryos exhibit extensive deficiencies in the development and organization of mesoderm-derived tissues and the musculoskeletal system. The Fgfr1 gene appears critical for the truncation of embryonic structures and formation of muscle and bone tissues and thereby the normal formation of limbs, skull, outer, middle, and inner ear, neural tube, tail, and lower spine as well as normal hearing.[6][8][9]

Clinical significance

Congenital diseases

Hereditary mutations in the FGFR1 gene are associated with various congenital malformations of the musculoskeletal system. Interstitial deletions at human chromosome 8p12-p11, arginine to a stop nonsense mutation at FGFR1 amino acid 622 (annotated as R622X), and numerous other autosomal dominant inactivating mutations in FGFR1 are responsible for ~10% of the cases of Kallmann syndrome. This syndrome is a form of hypogonadotropic hypogonadism associated in a varying percentage of cases with anosmia or hyposmia; cleft palate and other craniofacial defects; and scoliosis and other musculoskeletal malformations. An activating mutation in FGFR1 viz., P232R (proline-to-arginine substitution in the protein's 232nd amino acid), is responsible for the Type 1 or classic form of (Pfeiffer syndrome]], a disease characterized by craniosynostosis and mid-face deformities. A tyrosine-to-cysteine substitution mutation in the 372nd amino acid pf FGFR1 (Y372C) is responsible for some cases of Osteoglophonic dysplasia. This mutation results in craniosynostosis, mandibular prognathism, hypertelorism, brachydactyly, and inter-phalangeal joint fusion. Other inherited defects associated with 'FGFR1 mutations likewise involve musculoskeletal malformatios: these include the Jackson–Weiss syndrome (proline to arg substitution at amino acid 252), Antley-Bixler syndrome (isoleucine-to-threonine at amino acid 300 (I300T), and Trigonocephaly (mutation the same as the one for the Antley-Bixler syndrome viz., I300T).[5][6][10]

Cancers

Somatic mutations and epigenetic changes in the expression of the FGFR1 gene occur in and are thought to contribute to various types of lung, breast, hematological, and other types of cancers.

Lung cancers

Amplification of the FGFR1 gene (four or more copies) is present in 9 to 22% of patients with non-small-cell lung carcinoma (NSCLC). FGFR1 amplification was highly correlated with a history of tobacco smoking and proved to be the single largest prognostic factor in a cohort of patients suffering this disease. About 1% of patients with other types of lung cancer show amplifications in FGFR1.[4][5][11][12]

Breast cancers

Amplification of FGFR1 also occurs in ~10% of estrogen receptor positive breast cancers, particularly of the luminol subtype B form of breast cancer. The presence of FGFR1 amplification has been correlated with resistance to hormone blocking therapy and found to be a poor prognostic factor in the disease.[4][5]

Hematological cancers

In certain rare hematological cancers, the fusion of FGFR1 with various other genes due to Chromosomal translocations or Interstitial deletions create genes that encode chimeric FGFR1 Fusion proteins. These proteins have continuously active FGFR1-derived tyrosine kinase and thereby continuously stimulated the cell growth and proliferation. These mutations occur in the early stages of myeloid and/or lymphoid cell lines and are the cause of or contribute to the development and progression of certain types of hematological malignancies that have increased numbers of circulating blood eosinophils, increased numbers of bone marrow eosinophils, and/or the infiltration of eosinophils into tissues. These neoplasms were initially regarded as eosinophilias, hypereosinophilias, Myeloid leukemias, myeloproliferative neoplasms, myeloid sarcomas, lymphoid leukemias, or non-Hodgkin lymphomas. Based on their association with eosinophils, unique genetic mutations, and known or potential sensitivity to tyrosine kinase inhibitor therapy, they are now being classified together as clonal eosinophilias.[13] These mutations are described by connecting the chromosome site for the FGFR1 gene, 8p11 (i.e. human chromosome 8's short arm [i.e. p] at position 11) with another gene such as the MYO18A whose site is 17q11 (i.e human chromosome 17's long arm [i.e. q] at position 11) to yield the fusion gene annotated as t(8;17)(p11;q11). These FGFR1 mutations along with the chromosomal location of FGFR1A's partner gene and the annotation of the fused gene are given in the following table.[14][15][16]

Gene locus notation gene locus notation Gene locus notation gene locus notation gene locus notation
MYO18A 17q11 t(8;17)(p11;q11) CPSF6 12q15 t(8;12)(p11;q15) TPR 1q25 t(1;8)(q25p11;; HERV-K 10q13 t(8;13)(p11-q13) FGFR1OP2 12p11 t(8;12)(p11;q12)
ZMYM2 13q12 t(8;13)(p11;q12) CUTL1 7q22 t(7;8)(q22;p11) SQSTM1 5q35 t(5;8)(q35;p11 RANBP2 2q13 t(2;8)(q13;p11) LRRFIP1 2q37 t(8;2)(p11;q37)
CNTRL 9q33 t(8;9)(p11;q33) FGFR1OP 6q27 t(6;8)(q27;p11) BCR 22q11 t(8;22)(p11;q11 NUP98 11p15 t(8;11)(p11-p15) MYST3 8p11.21 muliple[17]
CEP110 16p12 t(8;16)(p11;p12)

These cancers are sometimes termed 8p11 myeloproliferative syndromes based on the chromosomal location of the FGFR1 gene. Translocations involving ZYMM2, CTRL, and GFGR10P2 are the most common forms of these 8p11 syndromes. In general, patients with any of these diseases have an average age of 44 and present with fatigue, night sweats, weight loss, fever, lymphadenopathy, and enlarged liver and/or spleen. They typically evidence hematological features of the myeloproliferative syndrome with moderate to greatly elevated levels of blood and bone marrow eosinophils. However, patients bearing: a) ZMYM2-FGFR1 fusion genes often present as T-cell lymphomas with spreading to non-lymphoid tissue; b) FPFR1-BCR fusion genes usually present as chronic myelogenous leukemias; c) CEP110 fusion genes may present as a chronic myelomonocytic leukemia with involvement of tonsil; and d) FPFR1-BCR or FGFR1-MYST3 fusion genes often present with little or no eosinophilia. Diagnosis requires conventional cytogenetics using Fluorescence in situ hybridization#Variations on probes and analysis with break-apart probes for FGFR1.[15][17]

Unlike many other myeloid neoplasms with eosinophil such as those caused by Platelet-derived growth factor receptor A or platelet-derived growth factor receptor B fusion genes, the myelodysplasia syndromes caused by FGFR1 fusion genes in general do not respond to tyrosine kinase inhibitors, are aggressive and rapidly progressive, and require treatment with chemotherapy agents followed by bone marrow transplantion in order to improve survival.[15][14] The tyrosine kinase inhibitor Ponatinib has been used as mono-therapy and subsequently used in combination with intensive chemotherapy to treat the myelodysplasia caused by the FGFR1-BCR fusion gene.[15]

Phosphaturic mesenchymal tumor

Phosphaturic mesenchymal tumors is characterized by a hypervascular proliferation of apparently non-malignant spindled cells associated with a variable amount of ‘smudgy’ calcified matrix but a small subset of these tumors exhibit malignant histological features and may behave in a clinically malignant fashion. In a series of 15 patients with this disease, 9 were found to have tumors that bore fusions between the FGFR1 gene and the FN1 gene located on human chromosome 2 at position q35.[18] The FGFR1-FN1 fusion gene was again identified in 16 of 39 (41%) patients with phosphaturic mesenchymal tumors.[19] The role of the(2;8)(35;11) FGFR1-FN1 fusion gene in this disease is not known.

Rhabdomyosarcoma

Elevated expression of FGFR1 protein was detected in 10 of 10 human Rhabdomyosarcoma tumors and 4 of 4 human cell lines derived from rhabdomyocarcoma. The tumor cases included 6 cases of Alveolar rhabdomyosarcoma, 2 cases of Embryonal rhabdomyosarcoma, and 2 cases of pleomorphic rhabdomyosarcoma. Rhabdomyosarcoma is a highly malignant form of cancer that develops from immature skeletal muscle cell precursors viz., myoblastss that have failed to fully differentiate. FGFR1 activation causes myoblast to proliferate while inhibiting their differentiation, dual effects that may lead to the assumption of a malignant phenotype by these cells. The 10 human rhabdomyosarcoma tumor exhibited decreased levels of methylation of CpG islands upstream of the first FGFR1 exon. CpG islands commonly function to silence expression of adjacent genes while their methylation inhibits this silencing. Hypomethylation of CpG islands upstream of FGFR1 is hypothesized to be at least in part responsible for the over-expression of FGFR1 by and malignant behavior of these rhabdomyosarcoma tumors.[20] In addition, a single case of rabdomyosarcoma tumor was found express co-amplified FOXO1 gene at 13q14 and FGFR1 gene at 8p11, i.e. t(8;13)(p11;q14), suggesting the formation, amplification, and malignant activity of a chimerical FOXO1-FGFR1 fusion gene by this tumor.[4][21]

Other types of cancers

Acquired abnormalities if the FGFR1 gene are found in: ~14% of urinary bladder Transitional cell carcinomas (almost all are amplifications); ~10% of squamous cell Head and neck cancers (~80% amplifications, 20% other mutations); ~7% of endometrial cancers (half amplifications, half other types of mutations); ~6% of prostate cancers (half amplifications, half other mutations); ~5% of ovarian Papillary serous cystadenocarcinoma (almost all amplifications); ~5% of colorectal cancers (~60 amplifications, 40% other mutations); ~4% of sarcomas (mostly amplifications); <3% of Glioblastomas (Fusion of FGFR1 and TACC1 (8p11) genes; <3% of Salivary gland cancer (all amplifications); and <2% in certain other cancers.[6][22][23]

FGFR inhibitors

Recent advances in our knowledge of the FGFR1 system has resulted in attempts to discover therapeutic touch points in the pathway for use in drug development. FGFR-targeted drugs exert direct as well as indirect anticancer effects, because FGFRs on cancer cells and endothelial cells are involved in tumorigenesis and vasculogenesis, respectively.[24] FGFR therapeutics are active as FGF affects numerous morphologies of cancers such as invasiveness, stemness and cellular survival. Primary among such drugs are antagonists. Small molecules that fit between the ATP binding pockets of the tyrosine kinase domains of the receptors. For FGFR1 numerous such small molecules are already approved for targeting of the structure of TKI ATP pocket. These include dovitinib and brivanib. The table below provides the IC50 (nanomolar) of small-molecule compounds targeting FGFRs.[24]

PD173074 Dovitinib Ki23057 Lenvatinib Brivanib Nintedanib Ponatinib MK-2461 Lucitanib AZD4547
26 8 NA 46 148 69 2.2 65 18 0.2

FGFR1 aberration in breast and lung cancer as a result of genetic over-amplification is effectively targeted using dovitinib and povatinib respectively.[25] Drug resistance is a highly relevant topic in the field of drug development for FGFR targets. FGFR inhibitors allow for the increase of tumor sensitivity to regular anticancer drug such as paclitaxel, and etoposide in human cancer cells and thereby enhancing antiapoptotic potential based on aberrant FGFR activation.[24] Moreover, FGF signaling inhibition dramatically reduces revascularization, hitting upon one of the hallmarks of cancers, angiogenesis, and reduces tumor burden in human tumors that depend on autocrine FGF signaling based on FGF2 upregulation following the common VEGFR-2 therapy for breast cancer. In such a way, FGFR1 can act synergistically with therapies to cut off cancer clonal resurgence by eliminating potential pathways of future relapse.[citation needed]

In addition, FGFR inhibitors are predicted to be effective on relapsed tumors because of the clonal evolution of an FGFR-activated minor subpopulation after therapy targeted to EGFRs or VEGFRs. Because there are multiple mechanisms of action for FGFR inhibitors to overcome drug resistance in human cancer, FGFR-targeted therapy is a promising strategy for the treatment of refractory cancer.[citation needed]

AZD4547 has undergone a phase II clinical trial (re gastric cancer) and reported some results.[26]

Lucitanib is an inhibitor of FGFR1 and FGFR2 and has undergone clinical trials for advanced solid tumors.[27]

Dovitinib (TKI258), an inhibitor of FGFR1, FGFR2, and FGFR3, has had a clinical trial on FGFR-amplified breast cancers.[28]

Interactions

Fibroblast growth factor receptor 1 has been shown to interact with:

See also

References

  1. ↑ Itoh N, Terachi T, Ohta M, Seo MK (Jun 1990). "The complete amino acid sequence of the shorter form of human basic fibroblast growth factor receptor deduced from its cDNA". Biochemical and Biophysical Research Communications. 169 (2): 680–5. doi:10.1016/0006-291X(90)90384-Y. PMID 2162671.
  2. ↑ https://www.ncbi.nlm.nih.gov/gene/2260
  3. ↑ Gonçalves C, Bastos M, Pignatelli D, Borges T, Aragüés JM, Fonseca F, Pereira BD, Socorro S, Lemos MC (2015). "Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform". Fertility and Sterility. 104 (5): 1261–7.e1. doi:10.1016/j.fertnstert.2015.07.1142. PMID 26277103.
  4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 Katoh M, Nakagama H (2014). "FGF receptors: cancer biology and therapeutics". Medicinal Research Reviews. 34 (2): 280–300. doi:10.1002/med.21288. PMID 23696246.
  5. ↑ 5.0 5.1 5.2 5.3 5.4 Kelleher FC, O'Sullivan H, Smyth E, McDermott R, Viterbo A (2013). "Fibroblast growth factor receptors, developmental corruption and malignant disease". Carcinogenesis. 34 (10): 2198–205. doi:10.1093/carcin/bgt254. PMID 23880303.
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 Helsten T, Schwaederle M, Kurzrock R (2015). "Fibroblast growth factor receptor signaling in hereditary and neoplastic disease: biologic and clinical implications". Cancer Metastasis Reviews. 34 (3): 479–96. doi:10.1007/s10555-015-9579-8. PMC 4573649. PMID 26224133.
  7. ↑ Bae JH, Lew, ED, Yuzawa S, Tome F, Lax I, Schlessinger J (Aug 2009). "The Selectivity of Receptor Tyrosine Kinase Signaling Is Controlled by a Secondary SH2 Domain Binding Site". Cell. 138 (3): 514–24. doi:10.1016/j.cell.2009.05.028. PMC 4764080. PMID 19665973.
  8. ↑ Deng C, Bedford M, Li C, Xu X, Yang X, Dunmore J, Leder P (1997). "Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development". Developmental Biology. 185 (1): 42–54. doi:10.1006/dbio.1997.8553. PMID 9169049.
  9. ↑ Calvert JA, Dedos SG, Hawker K, Fleming M, Lewis MA, Steel KP (2011). "A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice". Mammalian Genome. 22 (5–6): 290–305. doi:10.1007/s00335-011-9324-8. PMC 3099004. PMID 21479780.
  10. ↑ https://omim.org/entry/136350#editHistory
  11. ↑ https://pct.mdanderson.org/genes/fgfr1/show[full citation needed]
  12. ↑ Kim HR, Kim DJ, Kang DR, Lee JG, Lim SM, Lee CY, Rha SY, Bae MK, Lee YJ, Kim SH, Ha SJ, Soo RA, Chung KY, Kim JH, Lee JH, Shim HS, Cho BC (Feb 2013). "Fibroblast growth factor receptor 1 gene amplification is associated with poor survival and cigarette smoking dosage in patients with resected squamous cell lung cancer". Journal of Clinical Oncology. 31 (6): 731–7. doi:10.1200/JCO.2012.43.8622. PMID 23182986.
  13. ↑ Gotlib J (2015). "World Health Organization-defined eosinophilic disorders: 2015 update on diagnosis, risk stratification, and management". American Journal of Hematology. 90 (11): 1077–89. doi:10.1002/ajh.24196. PMID 26486351.
  14. ↑ 14.0 14.1 Vega F, Medeiros LJ, Bueso-Ramos CE, Arboleda P, Miranda RN (2015). "Hematolymphoid neoplasms associated with rearrangements of PDGFRA, PDGFRB, and FGFR1". American Journal of Clinical Pathology. 144 (3): 377–92. doi:10.1309/AJCPMORR5Z2IKCEM. PMID 26276769.
  15. ↑ 15.0 15.1 15.2 15.3 Reiter A, Gotlib J (2017). "Myeloid neoplasms with eosinophilia". Blood. 129 (6): 704–714. doi:10.1182/blood-2016-10-695973. PMID 28028030.
  16. ↑ Appiah-Kubi K, Lan T, Wang Y, Qian H, Wu M, Yao X, Wu Y, Chen Y (2017). "Platelet-derived growth factor receptors (PDGFRs) fusion genes involvement in hematological malignancies". Critical Reviews in Oncology/hematology. 109: 20–34. doi:10.1016/j.critrevonc.2016.11.008. PMID 28010895.
  17. ↑ 17.0 17.1 Patnaik MM, Gangat N, Knudson RA, Keefe JG, Hanson CA, Pardanani A, Ketterling RP, Tefferi A (2010). "Chromosome 8p11.2 translocations: prevalence, FISH analysis for FGFR1 and MYST3, and clinicopathologic correlates in a consecutive cohort of 13 cases from a single institution". American Journal of Hematology. 85 (4): 238–42. doi:10.1002/ajh.21631. PMID 20143402.
  18. ↑ Lee JC, Jeng YM, Su SY, Wu CT, Tsai KS, Lee CH, Lin CY, Carter JM, Huang JW, Chen SH, Shih SR, Mariño-Enríquez A, Chen CC, Folpe AL, Chang YL, Liang CW (2015). "Identification of a novel FN1-FGFR1 genetic fusion as a frequent event in phosphaturic mesenchymal tumour". The Journal of Pathology. 235 (4): 539–45. doi:10.1002/path.4465. PMID 25319834.
  19. ↑ Lee JC, Su SY, Changou CA, Yang RS, Tsai KS, Collins MT, Orwoll ES, Lin CY, Chen SH, Shih SR, Lee CH, Oda Y, Billings SD, Li CF, Nielsen GP, Konishi E, Petersson F, Carpenter TO, Sittampalam K, Huang HY, Folpe AL (2016). "Characterization of FN1-FGFR1 and novel FN1-FGF1 fusion genes in a large series of phosphaturic mesenchymal tumors". Modern Pathology. 29 (11): 1335–1346. doi:10.1038/modpathol.2016.137. PMID 27443518.
  20. ↑ Goldstein M, Meller I, Orr-Urtreger A (2007). "FGFR1 over-expression in primary rhabdomyosarcoma tumors is associated with hypomethylation of a 5' CpG island and abnormal expression of the AKT1, NOG, and BMP4 genes". Genes, Chromosomes & Cancer. 46 (11): 1028–38. doi:10.1002/gcc.20489. PMID 17696196.
  21. ↑ Liu J, Guzman MA, Pezanowski D, Patel D, Hauptman J, Keisling M, Hou SJ, Papenhausen PR, Pascasio JM, Punnett HH, Halligan GE, de Chadarévian JP (2011). "FOXO1-FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma". Modern Pathology. 24 (10): 1327–35. doi:10.1038/modpathol.2011.98. PMID 21666686.
  22. ↑ Singh D, Chan JM, Zoppoli P, Niola F, Sullivan R, Castano A, Liu EM, Reichel J, Porrati P, Pellegatta S, Qiu K, Gao Z, Ceccarelli M, Riccardi R, Brat DJ, Guha A, Aldape K, Golfinos JG, Zagzag D, Mikkelsen T, Finocchiaro G, Lasorella A, Rabadan R, Iavarone A (2012). "Transforming fusions of FGFR and TACC genes in human glioblastoma". Science. 337 (6099): 1231–5. doi:10.1126/science.1220834. PMC 3677224. PMID 22837387.
  23. ↑ Ach T, Schwarz-Furlan S, Ach S, Agaimy A, Gerken M, Rohrmeier C, Zenk J, Iro H, Brockhoff G, Ettl T (2016). "Genomic aberrations of MDM2, MDM4, FGFR1 and FGFR3 are associated with poor outcome in patients with salivary gland cancer". Journal of Oral Pathology & Medicine. 45 (7): 500–9. doi:10.1111/jop.12394. PMID 26661925.
  24. ↑ 24.0 24.1 24.2 Katoh M, Nakagama H (Mar 2014). "FGF receptors: cancer biology and therapeutics". Medicinal Research Reviews. 34 (2): 280–300. doi:10.1002/med.21288. PMID 23696246.
  25. ↑ André F, Bachelot T, Campone M, Dalenc F, Perez-Garcia JM, Hurvitz SA, et al. (2013). "Targeting FGFR with dovitinib (TKI258): preclinical and clinical data in breast cancer". Clinical Cancer Research. 19 (13): 3693–702. doi:10.1158/1078-0432.CCR-13-0190. PMID 23658459.
  26. ↑ A randomized, open-label phase II study of AZD4547 (AZD) versus Paclitaxel (P) in previously treated patients with advanced gastric cancer (AGC) with Fibroblast Growth Factor Receptor 2 (FGFR2) polysomy or gene amplification (amp): SHINE study.
  27. ↑ Soria; et al. (2014). "Phase I/IIa study evaluating the safety, efficacy, pharmacokinetics, and pharmacodynamics of lucitanib in advanced solid tumors". Ann. Oncol. 25: 2244–51. doi:10.1093/annonc/mdu390. PMID 25193991.
  28. ↑ André F, Bachelot T, Campone M, Dalenc F, Perez-Garcia JM, Hurvitz SA, Turner N, Rugo H, Smith JW, Deudon S, Shi M, Zhang Y, Kay A, Porta DG, Yovine A, Baselga J (2013). "Targeting FGFR with dovitinib (TKI258): preclinical and clinical data in breast cancer". Clin. Cancer Res. 19: 3693–702. doi:10.1158/1078-0432.CCR-13-0190. PMID 23658459.
  29. ↑ Schlessinger J, Plotnikov AN, Ibrahimi OA, Eliseenkova AV, Yeh BK, Yayon A, Linhardt RJ, Mohammadi M (Sep 2000). "Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization". Mol. Cell. 6 (3): 743–50. doi:10.1016/s1097-2765(00)00073-3. PMID 11030354.
  30. ↑ Santos-Ocampo S, Colvin JS, Chellaiah A, Ornitz DM (Jan 1996). "Expression and biological activity of mouse fibroblast growth factor-9". J. Biol. Chem. 271 (3): 1726–31. doi:10.1074/jbc.271.3.1726. PMID 8576175.
  31. ↑ Yan KS, Kuti M, Yan S, Mujtaba S, Farooq A, Goldfarb MP, Zhou MM (May 2002). "FRS2 PTB domain conformation regulates interactions with divergent neurotrophic receptors". J. Biol. Chem. 277 (19): 17088–94. doi:10.1074/jbc.M107963200. PMID 11877385.
  32. ↑ Ong SH, Guy GR, Hadari YR, Laks S, Gotoh N, Schlessinger J, Lax I (Feb 2000). "FRS2 proteins recruit intracellular signaling pathways by binding to diverse targets on fibroblast growth factor and nerve growth factor receptors". Mol. Cell. Biol. 20 (3): 979–89. doi:10.1128/mcb.20.3.979-989.2000. PMC 85215. PMID 10629055.
  33. ↑ Xu H, Lee KW, Goldfarb M (Jul 1998). "Novel recognition motif on fibroblast growth factor receptor mediates direct association and activation of SNT adapter proteins". J. Biol. Chem. 273 (29): 17987–90. doi:10.1074/jbc.273.29.17987. PMID 9660748.
  34. ↑ Dhalluin C, Yan KS, Plotnikova O, Lee KW, Zeng L, Kuti M, Mujtaba S, Goldfarb MP, Zhou MM (Oct 2000). "Structural basis of SNT PTB domain interactions with distinct neurotrophic receptors". Mol. Cell. 6 (4): 921–9. doi:10.1016/S1097-2765(05)00087-0. PMID 11090629.
  35. ↑ Urakawa I, Yamazaki Y, Shimada T, Iijima K, Hasegawa H, Okawa K, Fujita T, Fukumoto S, Yamashita T (Dec 2006). "Klotho converts canonical FGF receptor into a specific receptor for FGF23". Nature. 444 (7120): 770–4. Bibcode:2006Natur.444..770U. doi:10.1038/nature05315. PMID 17086194.
  36. ↑ Reilly JF, Mickey G, Maher PA (Mar 2000). "Association of fibroblast growth factor receptor 1 with the adaptor protein Grb14. Characterization of a new receptor binding partner". J. Biol. Chem. 275 (11): 7771–8. doi:10.1074/jbc.275.11.7771. PMID 10713090.
  37. ↑ Karlsson T, Songyang Z, Landgren E, Lavergne C, Di Fiore PP, Anafi M, Pawson T, Cantley LC, Claesson-Welsh L, Welsh M (Apr 1995). "Molecular interactions of the Src homology 2 domain protein Shb with phosphotyrosine residues, tyrosine kinase receptors and Src homology 3 domain proteins". Oncogene. 10 (8): 1475–83. PMID 7537362.

Further reading

External links

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