Elesclomol
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| Formula | C19H20N4O2S2 |
| Molar mass | 400.52 g·mol−1 |
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Elesclomol (INN, codenamed STA-4783) is a drug that triggers apoptosis (programmed cell death) in cancer cells. It is being developed by Synta Pharmaceuticals and GlaxoSmithKline as a chemotherapy adjuvant, and has received both fast track and orphan drug status from the U.S. Food and Drug Administration for the treatment of metastatic melanoma.[1] Synta Pharmaceuticals announced on February 26, 2009 the suspension of all clinical trials involving Elesclomol due to safety concerns.[2] In March 2010, Synta announced that the FDA had approved resuming clinical development of elesclomol, and that they expected to initiate one or more clinical trials for elesclomol in the second half of the year.[3]
In a small, randomized phase II study, elesclomol was shown to significantly increase progression-free survival in people with metastatic melanoma when given in addition to paclitaxel (Taxol).[4][5]
Results from a phase III trial were announced in March 2013. The study was halted when it was determined that addition of elesclomol to paclitaxel didn't significantly increase progression-free survival.[6]
Studies in preclinical models suggested that Elesclomol may be effective in Ewing sarcoma cells with elevated levels of cellular oxidative stress.[7]
Mechanism of action[edit]
Elesclomol induces oxidative stress by provoking a buildup of reactive oxygen species within cancer cells.[8] Elesclomol requires a redox active metal ion to function. The Cu(II) complex is 34 times more potent than the Ni(II) complex and 1040-fold more potent than the Pt(II) complex.[9]
Discovery[edit]
Elesclomol was first synthesized at Shinogi BioResearch in Lexington, MA. Its efficacy against cancer was discovered by scientists at Shionogi BioResearch. “It was pure chemist’s joy,” Synta's Chen said. “Homemade, random, and clearly made for no particular purpose. It was the only one that worked on everything we tried.”[10]
References[edit]
- ^ "Synta And GlaxoSmithKline Announce Elesclomol Granted Orphan Drug Designation By The FDA" (Press release). Medical News Today. January 30, 2008. Archived from the original on December 8, 2008. Retrieved November 30, 2008. Retrieved November 30, 2008.
- ^ "Synta Pharmaceuticals press release". February 26, 2009. Archived from the original on July 12, 2012.
- ^ "Synta Announces Elesclomol Clinical Development to Resume". March 2, 2010.
- ^ "Prous Science Molecule of the Month: Elesclomol". Thomson Reuters. December 2007. Archived from the original on 2008-02-20. Retrieved November 30, 2008.
- ^ Qu Y, Wang J, Sim MS, Liu B, Giuliano A, Barsoum J, Cui X (June 2010). "Elesclomol, counteracted by Akt survival signaling, enhances the apoptotic effect of chemotherapy drugs in breast cancer cells". Breast Cancer Research and Treatment. 121 (2): 311–21. doi:10.1007/s10549-009-0470-6. PMID 19609669. S2CID 1312270.
- ^ O'Day SJ, Eggermont AM, Chiarion-Sileni V, Kefford R, Grob JJ, Mortier L, et al. (March 2013). "Final results of phase III SYMMETRY study: randomized, double-blind trial of elesclomol plus paclitaxel versus paclitaxel alone as treatment for chemotherapy-naive patients with advanced melanoma". Journal of Clinical Oncology. 31 (9): 1211–8. doi:10.1200/JCO.2012.44.5585. PMID 23401447.
- ^ Marchetto A, Ohmura S, Orth MF, Knott MM, Colombo MV, Arrigoni C, et al. (May 2020). "Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma". Nature Communications. 11 (1): 2423. Bibcode:2020NatCo..11.2423M. doi:10.1038/s41467-020-16244-2. PMC 7228971. PMID 32415069.
- ^ Kirshner JR, He S, Balasubramanyam V, Kepros J, Yang CY, Zhang M, et al. (August 2008). "Elesclomol induces cancer cell apoptosis through oxidative stress". Molecular Cancer Therapeutics. 7 (8): 2319–27. doi:10.1158/1535-7163.MCT-08-0298. PMID 18723479.
- ^ Yadav AA, Patel D, Wu X, Hasinoff BB (September 2013). "Molecular mechanisms of the biological activity of the anticancer drug elesclomol and its complexes with Cu(II), Ni(II) and Pt(II)". Journal of Inorganic Biochemistry. 126: 1–6. doi:10.1016/j.jinorgbio.2013.04.013. PMID 23707906. S2CID 20624982.
- ^ Gladwell M (17 May 2010). "The Treatment - Why is it so difficult to develop drugs for cancer?". The New Yorker. Retrieved 13 September 2014.
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