| Literature DB >> 18049476 |
T Bruno1, S Iezzi, F De Nicola, M Di Padova, A Desantis, M Scarsella, M G Di Certo, C Leonetti, A Floridi, C Passananti, M Fanciulli.
Abstract
X-linked inhibitor of apoptosis protein (XIAP) is a member of the inhibitor of apoptosis proteins family that selectively binds and inhibits caspase-3, -7 and -9. As such, XIAP is an extremely potent suppressor of apoptosis and an attractive target for cancer treatment. Che-1 is an antiapoptotic agent involved in the control of gene transcription and cell proliferation. Recently, we showed that the checkpoint kinases ATM/ATR and checkpoint kinase 2 physically and functionally interact with Che-1 and promote its phosphorylation and accumulation in response to DNA damage. These Che-1 modifications induce transcription of p53, and Che-1 depletion strongly sensitizes tumor cells to anticancer drugs. Here we show that Che-1 activates XIAP expression in response to DNA damage. This effect is mediated by Che-1 phosphorylation and requires NF-kappaB. Notably, we found that XIAP expression is necessary for antiapoptotic activity of Che-1 and that in vivo downregulation of Che-1 by small interference RNA strongly enhanced the cytotoxicity of anticancer drugs.Entities:
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Year: 2007 PMID: 18049476 DOI: 10.1038/sj.cdd.4402284
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828