| Literature DB >> 18022360 |
Hao Wu1, Jurg Tschopp, Su-Chang Lin.
Abstract
Inhibitor of apoptosis proteins (IAPs) such as XIAP, cIAP1, and cIAP2 are upregulated in many cancer cells. It has been thought that small-molecule mimetics of Smac, an endogenous IAP antagonist, might potentiate apoptosis in cancer cells by promoting caspase activation. However, three recent papers, two in Cell (Vince et al., 2007; Varfolomeev et al., 2007) and one in Cancer Cell (Petersen et al., 2007), now report that Smac mimetics primarily kill cancer cells via a different mechanism, the induction of autoubiquitination and degradation of cIAPs, which culminates in TNFalpha-mediated cell death.Entities:
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Year: 2007 PMID: 18022360 PMCID: PMC3184251 DOI: 10.1016/j.cell.2007.10.042
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582