Gastrointestinal stromal tumor pathophysiology
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Parminder Dhingra, M.D. [2]
Overview
The exact pathogenesis of [disease name] is not fully understood.
OR
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype. On microscopic histopathological analysis, spindle cells or plump epithelioid cells are characteristic findings of gastrointestinal stromal tumor.
Pathophysiology
- Gastrointestinal stromal tumors (GISTs) are rare but the most common mesenchymal (nonepithelial) tumors of the gastrointestinal tract.[1]
- GIST tumors can either be benign tumors or massive malignant tumors with widespread metastasis.
- Earlier GIST were thought to arise from the submucosal or smooth muscle cells of the GI tract. However recent research have proved that GISTs are derived from the interstitial cells of Cajal or undifferentiated precursor cells that finally develop into interstitial cells of Cajal.
- Interstitial cells of Cajal (ICC) are a normal part of myenteric plexus and the autonomic nervous system of the intestine.
- Interstitial cells of Cajal serve as a pacemaker of intestine and controls intestinal motility.[2][3]
- Molecular analysis has shown that GISTs arising from the interstitial cells of Cajal, stain positive for CD117 (c-KIT) in 90% cases and CD34 in 70% of cases. Around 5% of the cases are positive for PDGFRA. The rest of the cases are defined as wild type (negative for both CD117 and PDGFRA).
- CD117 is encoded by the KIT gene. Other names for CD117 include proto-oncogene c-Kit and tyrosine kinase receptor Kit.
- CD34 is the myeloid progenitor cell antigen and also known as hematopoietic progenitor cell antigen CD34.
- PDGFRA is platelet derived growth factor receptor-alpha and is a tyrosine kinase receptor.
- GIST can occur in any part of the gastrointestinal tract. Thus, GIST vary considerably in their presentation and clinical course, ranging from being asymptomatic to presenting with severe signs and symptoms of bleeding, abdominal pain and perforation.
- The most common location for GIST is the stomach with the second most common location as the small intestine.
- Less frequent sites of occurrence include the colon, rectum and esophagus.
- Rare sites include pancreas, peritoneum, omentum, or mesentery.[4]
- GIST (tumors) can grow as an endophytic or exophytic lesions.
- Endophytic lesions are benign linear lesions that grow along the lumen of the affected organ.
- Exophytic lesions can present as a protruding outgrowth outside the lumen of the GI tract.
- GIST have a variable malignant potential.[5]
Genetics
Genes involved in the pathogenesis of gastrointestinal stromal tumors include mutations in c-Kit gene and PDGFRA (platelet derived growth factor receptor-alpha) gene. In some rare cases where the patient do not exhibit the typical c-Kit and PDGFRA mutation, reports of mutation in succinate dehydrogenase (SDH) . Rare genes involved include BRAF kinase, and protein kinase C. The majority of GISTs are sporadic in origin. [8][9][10][11]
- The c-kit gene is a proto-oncogene and located on chromosome 4q11-12 (long (q) arm of chromosome 4 at position 12).
- The c-kit gene encodes for KIT protein which is a transmembrane tyrosine kinase.
- The KIT protein is located on the cell membrane of certain cell types.
- Stem cell factor is the ligand that binds to KIT protein, which in turn leads to activation of KIT protein.
- Upon activation, the KIT protein leads to activation of other intracellular proteins by a process known as phosphorylation (which involves adding oxygen and phosphorus at specific positions).
- The activation of these intracellular proteins such as (MAP kinase and RAS) plays a vital role in multiple signaling pathways.
- The signaling pathways stimulated by the KIT protein control many important cellular processes such as cell growth and proliferation.
- In addition, KIT protein signaling also has a role in the development of gastrointestinal tract cells known as interstitial cells of Cajal.
- The most commonly observed mutation site in c-Kit gene involves exon 11 leading to a gain-of-function mutation. Less common sites include exons 9 and 13.
- Gain of function mutation leads to overexpression and autophosphorylation of c-Kit that leads to inhibition of apoptosis and uncontrolled cell proliferation.
- Almost 90-95% of patients with GIST have mutated c-Kit gene.
- C-Kit (a tyrosine kinase growth factor receptor) is also the target of medical therapy in GIST; ST-571 (Imatinib; Glivec).
- About 10% cases of GIST are associated with PDGFRA gene.
- The PDGFRA gene is located on chromosome 4q11-12 (long (q) arm of chromosome 4 at position 12).
- The PDGFRA gene encodes for the protein; platelet-derived growth factor receptor alpha (PDGFRA), which belongs to a family of proteins known as receptor tyrosine kinases.
- The platelet-derived growth factor is the ligand that binds to PDGFRA ,which in turn activates the PDGFRA.
- Upon activation, the PDGFRA leads to activation of other intracellular proteins by a process known as phosphorylation (same as c-Kit explained above).
- The activation of these intracellular proteins such as (MAP kinase and RAS) plays a vital role in multiple signaling pathways.
- The multiple signaling pathways stimulated by PDGFRA gene control many important cellular processes such as cell growth and proliferation.
- The most commonly observed mutation site in PDGFRA gene involves exon 18.
- As a result of mutation, the PDGFRA gene gets activated on its own and leads to inhibition of apoptosis and uncontrolled cell proliferation.
| Gastrointestinal stromal tumors | |||||||||||||||||||||||||||||||||||||||||||||
| KIT gene mutation | PDGFRA mutation | Wild type (absence of KIT/PDGFRA) | |||||||||||||||||||||||||||||||||||||||||||
| Exon 9,13 & 17 | Exon 11 | Mutant succinate dehydrogenase | |||||||||||||||||||||||||||||||||||||||||||
| Uncontrolled KIT signalling | KIT receptor mutation | Dysfunction of electron transport mitochondria | |||||||||||||||||||||||||||||||||||||||||||
| Defective oxidative phosphorylation | |||||||||||||||||||||||||||||||||||||||||||||
| Abnormal stabilization of HIF | |||||||||||||||||||||||||||||||||||||||||||||
Associated Conditions
- Urticaria pigmentosa
- Neurofibromatosis type 1
- Carney-Stratakis syndrome
Gross Pathology
On gross pathology, GISTs have the following findings:
- Rounded appearance with areas of hemorrhage.
- Large tumors may have necrosis or cystic change.
- Variable size (ranging from 1 to 30cms).
Microscopic Pathology
On microscopic histopathological analysis, GISTs are cellular tumors arising from muscularis propria and composed of:[12]
- Spindle cells (60%-80%): Spindle cells have a fascicular or whorled like appearance and are made of multiple compact cells with minimal stroma and eosinophilic, basophilic or amphophilic cytoplasm. The CD117 expression in spindle cells are generally diffuse and strong.
- Epithelioid cells (20%-30%): Epithelioid tumors are clearly defined with an abundant cytoplasm which is amphophilic to clear. The CD117 expression in epithelioid cells is generally focal and weakly positive.
- Spindle cells or epithelioid cells (10%).
Pathogenesis
- The exact pathogenesis of [disease name] is not fully understood.
OR
- It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
References
- ↑ Miettinen M, Lasota J (2001). "Gastrointestinal stromal tumors--definition, clinical, histological, immunohistochemical, and molecular genetic features and differential diagnosis". Virchows Arch. 438 (1): 1–12. PMID 11213830.
- ↑ Miettinen M, Lasota J (2006). "Gastrointestinal stromal tumors: review on morphology, molecular pathology, prognosis, and differential diagnosis". Arch Pathol Lab Med. 130 (10): 1466–78. PMID 17090188.
- ↑ Kindblom LG, Remotti HE, Aldenborg F, Meis-Kindblom JM (1998). "Gastrointestinal pacemaker cell tumor (GIPACT): gastrointestinal stromal tumors show phenotypic characteristics of the interstitial cells of Cajal". Am. J. Pathol. 152 (5): 1259–69. PMC 1858579. PMID 9588894.
- ↑ Reith JD, Goldblum JR, Lyles RH, Weiss SW (2000). "Extragastrointestinal (soft tissue) stromal tumors: an analysis of 48 cases with emphasis on histologic predictors of outcome". Mod. Pathol. 13 (5): 577–85. doi:10.1038/modpathol.3880099. PMID 10824931.
- ↑ Joensuu H, Vehtari A, Riihimäki J, Nishida T, Steigen SE, Brabec P, Plank L, Nilsson B, Cirilli C, Braconi C, Bordoni A, Magnusson MK, Linke Z, Sufliarsky J, Federico M, Jonasson JG, Dei Tos AP, Rutkowski P (2012). "Risk of recurrence of gastrointestinal stromal tumour after surgery: an analysis of pooled population-based cohorts". Lancet Oncol. 13 (3): 265–74. doi:10.1016/S1470-2045(11)70299-6. PMID 22153892.
- ↑ Woodall CE, Brock GN, Fan J, Byam JA, Scoggins CR, McMasters KM, Martin RC (2009). "An evaluation of 2537 gastrointestinal stromal tumors for a proposed clinical staging system". Arch Surg. 144 (7): 670–8. doi:10.1001/archsurg.2009.108. PMID 19620548.
- ↑ Emile JF, Brahimi S, Coindre JM, Bringuier PP, Monges G, Samb P, Doucet L, Hostein I, Landi B, Buisine MP, Neuville A, Bouché O, Cervera P, Pretet JL, Tisserand J, Gauthier A, Le Cesne A, Sabourin JC, Scoazec JY, Bonvalot S, Corless CL, Heinrich MC, Blay JY, Aegerter P (2012). "Frequencies of KIT and PDGFRA mutations in the MolecGIST prospective population-based study differ from those of advanced GISTs". Med. Oncol. 29 (3): 1765–72. doi:10.1007/s12032-011-0074-y. PMID 21953054.
- ↑ Heinrich MC, Corless CL, Demetri GD, Blanke CD, von Mehren M, Joensuu H, McGreevey LS, Chen CJ, Van den Abbeele AD, Druker BJ, Kiese B, Eisenberg B, Roberts PJ, Singer S, Fletcher CD, Silberman S, Dimitrijevic S, Fletcher JA (2003). "Kinase mutations and imatinib response in patients with metastatic gastrointestinal stromal tumor". J. Clin. Oncol. 21 (23): 4342–9. doi:10.1200/JCO.2003.04.190. PMID 14645423.
- ↑ Hirota S, Isozaki K, Moriyama Y, Hashimoto K, Nishida T, Ishiguro S, Kawano K, Hanada M, Kurata A, Takeda M, Muhammad Tunio G, Matsuzawa Y, Kanakura Y, Shinomura Y, Kitamura Y (1998). "Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors". Science. 279 (5350): 577–80. PMID 9438854.
- ↑ Duensing, Anette; Medeiros, Fabiola; McConarty, Bryna; Joseph, Nora E; Panigrahy, Dipak; Singer, Samuel; Fletcher, Christopher DM; Demetri, George D; Fletcher, Jonathan A (2004). "Mechanisms of oncogenic KIT signal transduction in primary gastrointestinal stromal tumors (GISTs)". Oncogene. 23 (22): 3999–4006. doi:10.1038/sj.onc.1207525. ISSN 0950-9232.
- ↑ Lux, Marcia L.; Rubin, Brian P.; Biase, Tara L.; Chen, Chang-Jie; Maclure, Timothy; Demetri, George; Xiao, Sheng; Singer, Samuel; Fletcher, Christopher D.M.; Fletcher, Jonathan A. (2000). "KIT Extracellular and Kinase Domain Mutations in Gastrointestinal Stromal Tumors". The American Journal of Pathology. 156 (3): 791–795. doi:10.1016/S0002-9440(10)64946-2. ISSN 0002-9440.
- ↑ "Gastrointestinal stromal tumour".