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• W2904142983 abstract "Aberrant regulation of programmed cell death (PCD) has been tied to an array of human pathologies ranging from cancers to autoimmune disorders to diverse forms of neurodegeneration. Pharmacologic modulation of PCD signalling is therefore of central interest to a number of clinical and biomedical applications. A key component of PCD signalling involves the modulation of pro- and anti-apoptotic Bcl-2 family members. Among these, Bax translocation represents a critical regulatory phase in PCD. In the present study, we have employed a high-content high-throughput screen to identify small molecules which inhibit the cellular process of Bax re-distribution to the mitochondria following commitment of the cell to die. Screening of 6246 Generally Recognized As Safe compounds from four chemical libraries post-induction of cisplatin-mediated PCD resulted in the identification of 18 compounds which significantly reduced levels of Bax translocation. Further examination revealed protective effects via reduction of executioner caspase activity and enhanced mitochondrial function. Consistent with their effects on Bax translocation, these compounds exhibited significant rescue against in vitro and in vivo cisplatin-induced apoptosis. Altogether, our findings identify a new set of clinically useful small molecules PCD inhibitors and highlight the role which cAMP plays in regulating Bax-mediated PCD." @default.
• W2904142983 created "2018-12-22" @default.
• W2904142983 creator A5004445832 @default.
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• W2904142983 date "2018-12-13" @default.
• W2904142983 modified "2023-10-17" @default.
• W2904142983 title "Cell‐based high‐throughput screen for small molecule inhibitors of Bax translocation" @default.
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• W2904142983 doi "https://doi.org/10.1111/jcmm.14076" @default.
• W2904142983 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6378228" @default.
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• W2904142983 hasPublicationYear "2018" @default.
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