Salinosporamide A

Jump to navigation Jump to search

Template:Chembox new

WikiDoc Resources for Salinosporamide A

Articles

Most recent articles on Salinosporamide A

Most cited articles on Salinosporamide A

Review articles on Salinosporamide A

Articles on Salinosporamide A in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Salinosporamide A

Images of Salinosporamide A

Photos of Salinosporamide A

Podcasts & MP3s on Salinosporamide A

Videos on Salinosporamide A

Evidence Based Medicine

Cochrane Collaboration on Salinosporamide A

Bandolier on Salinosporamide A

TRIP on Salinosporamide A

Clinical Trials

Ongoing Trials on Salinosporamide A at Clinical Trials.gov

Trial results on Salinosporamide A

Clinical Trials on Salinosporamide A at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Salinosporamide A

NICE Guidance on Salinosporamide A

NHS PRODIGY Guidance

FDA on Salinosporamide A

CDC on Salinosporamide A

Books

Books on Salinosporamide A

News

Salinosporamide A in the news

Be alerted to news on Salinosporamide A

News trends on Salinosporamide A

Commentary

Blogs on Salinosporamide A

Definitions

Definitions of Salinosporamide A

Patient Resources / Community

Patient resources on Salinosporamide A

Discussion groups on Salinosporamide A

Patient Handouts on Salinosporamide A

Directions to Hospitals Treating Salinosporamide A

Risk calculators and risk factors for Salinosporamide A

Healthcare Provider Resources

Symptoms of Salinosporamide A

Causes & Risk Factors for Salinosporamide A

Diagnostic studies for Salinosporamide A

Treatment of Salinosporamide A

Continuing Medical Education (CME)

CME Programs on Salinosporamide A

International

Salinosporamide A en Espanol

Salinosporamide A en Francais

Business

Salinosporamide A in the Marketplace

Patents on Salinosporamide A

Experimental / Informatics

List of terms related to Salinosporamide A


Salinosporamide A is a potent proteasome inhibitor used as an anticancer agent that recently entered phase I human clinical trials for the treatment of multiple myeloma only three years after its discovery.[1][2] This novel marine natural product is produced by the recently described obligate marine bacterium Salinispora tropica which is found in ocean sediment. Salinosporamide A belongs to a family of compounds possesing a densely functionalized γ-lactam-β-lactone bicycle.

History

In preliminary screening, a high percentage of the organic extracts of cultured Salinospora strains possessed antibiotic and anticancer activities, which suggests that these bacteria are an excellent resource for drug discovery. Salinospora strain CNB-392 was isolated from a heat-treated marine sediment sample and cytotoxicity-guided fractionation of the crude extract led to the isolation of salinosporamide A. Although salinosporamide A shares an identical bicyclic ring structure with omuralide, it is uniquely functionalized. Salinosporamide A displayed potent in vitro cytotoxicity against HCT-116 human colon carcinoma with an IC50 value of 11 ng mL-1. This compound also displayed potent and highly selective activity in the NCI's 60-cell-line panel with a mean GI50 value (the concentration required to achieve 50 % growth inhibition) of less than 10 nM and a greater than 4 log LC50 differential between resistant and susceptible cell lines. The greatest potency was observed against NCI-H226 non-small cell lung cancer, SF-539 CNS cancer, SK-MEL-28 melanoma, and MDA-MB-435 breast cancer (all with LC50 values less than 10 nM). Salinosporamide A was tested for its effects on proteasome function because of its structural relationship to omuralide. When tested against purified 20S proteasome, salinosporamide A inhibited proteasomal chymotrypsin-like proteolytic activity with an IC50 value of 1.3 nM.[3] This compound is approximately 35 times more potent than omuralide which was tested as a positive control in the same assay. Thus, the unique functionalization of the core bicyclic ring structure of salinosporamide A appears to have resulted in a molecule that is a significantly more potent proteasome inhibitor than omuralide.[1]

Mechanism of action

Salinosporamide A inhibits proteasome activity by covalently modifying the active site threonine residues of the 20S proteasome.

Biosynthesis

Salinosporamide A and B building Blocks
Proposed Biosynthesis of the Nonproteinogenic amino-acid beta-hydroxycyclohex-2'-enylanine (3) (R = H or S~PCP) via a Shunt in the Phenylalanine Biosynthetic Pathway
Biosynthesis

It was originally hypothesized that Salinosporamide B was a biosynthetic precursor to Salinosporamide A due to their structural similarities.

It was thought that the halogenation of the unactivated methyl group was catalyzed by a non-heme iron halogenase[4][5]. Recent work using 13C-labeled feeding experiments reveal distinct biosynthetic origins of salinosporamide A and B.[4][6]

While they share the biosynthetic precursors acetate and presumed β-hydroxycyclohex-2'-enylalanine (3), they differ in the origin of the four-carbon building block that gives rise to their structural differences involving the halogen atom. A hybrid polyketide synthase-nonribosomal peptide synthetase (PKS-NRPS) pathway is most likely the biosynthetic mechanism in which acetyl-CoA and butyrate-derived ethylmalonyl-CoA condense to yield the β-ketothioester (4), which then reacts with (3) to generate the linear precursor (5).

Total synthesis

First stereoselective sythesis was reported by Rajender Reddy and E. J.Corey. [7] Later several routes to the total synthesis of Salinosporamide A have been reported.[8][9][10][7]

Clinical use

In vitro studies using purified 20S proteasomes showed that Salinosporamide A has lower EC50 for trypsin-like (T-L) activity than does Bortezomib. In vivo animal model studies show marked inhibition of T-L activity in response to Salinosporamide A, whereas Bortezomib enhances T-L proteasome activity.

References

  1. 1.0 1.1 Feling RH, Buchanan GO, Mincer TJ, Kauffman CA, Jensen PR, Fenical W (2003). "Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora". Angew. Chem. Int. Ed. Engl. 42 (3): 355–7. doi:10.1002/anie.200390115. PMID 12548698.
  2. Chauhan D, Catley L, Li G; et al. (2005). "A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib". Cancer Cell. 8 (5): 407–19. doi:10.1016/j.ccr.2005.10.013. PMID 16286248.
  3. K. Lloyd, S. Glaser, B. Miller, Nereus Pharmaceuticals Inc.
  4. 4.0 4.1 Beer LL, Moore BS (2007). "Biosynthetic convergence of salinosporamides A and B in the marine actinomycete Salinispora tropica". Org. Lett. 9 (5): 845–8. doi:10.1021/ol063102o. PMID 17274624.
  5. Vaillancourt FH, Yeh E, Vosburg DA, Garneau-Tsodikova S, Walsh CT (2006). "Nature's inventory of halogenation catalysts: oxidative strategies predominate". Chem. Rev. 106 (8): 3364–78. doi:10.1021/cr050313i. PMID 16895332.
  6. Tsueng G, McArthur KA, Potts BC, Lam KS (2007). "Unique butyric acid incorporation patterns for salinosporamides A and B reveal distinct biosynthetic origins". doi:10.1007/s00253-007-0899-7. PMID 17340108.
  7. 7.0 7.1 Reddy LR, Saravanan P, Corey EJ (2004). "A simple stereocontrolled synthesis of salinosporamide A". J. Am. Chem. Soc. 126 (20): 6230–1. doi:10.1021/ja048613p. PMID 15149210.
  8. Ling T, Macherla VR, Manam RR, McArthur KA, Potts BC (2007). "Enantioselective Total Synthesis of (-)-Salinosporamide A (NPI-0052)". Org. Lett. 9 (12): 2289–92. doi:10.1021/ol0706051. PMID 17497868.
  9. Ma G, Nguyen H, Romo D (2007). "Concise total synthesis of (+/-)-salinosporamide A, (+/-)-cinnabaramide A, and derivatives via a bis-cyclization process: implications for a biosynthetic pathway?". Org. Lett. 9 (11): 2143–6. doi:10.1021/ol070616u. PMID 17477539.
  10. Endo A, Danishefsky SJ (2005). "Total synthesis of salinosporamide A". J. Am. Chem. Soc. 127 (23): 8298–9. doi:10.1021/ja0522783. PMID 15941259.



Template:WikiDoc Sources