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Antagonizing XIAP-mediated caspase-3 inhibition. Achilles' heel of cancers?

机译:拮抗XIAP介导的caspase-3抑制。致命的致命弱点?

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In this issue of Cancer Cell, Schimmer et al. report the identification of small molecule antagonists of XIAP that overcome its inhibition of caspase-3. It was remarkable that the compounds directly induced cell death in tumor cells while having little toxicity on normal cells. This suggests that caspases are already activated in tumor cells, which is different from the caspase activation status in normal mammalian cells. In comparison with Smac peptides targeting XIAP-mediated caspase-9 inhibition, which do not directly induce cell death, it appears that liberating downstream caspases rather than upstream caspases may be a preferred strategy for cancer drug discovery.
机译:在本期《癌细胞》中,Schimmer等人。报告鉴定了克服其对caspase-3抑制作用的XIAP小分子拮抗剂。值得注意的是,这些化合物直接诱导肿瘤细胞死亡,而对正常细胞几乎没有毒性。这表明胱天蛋白酶在肿瘤细胞中已经被激活,这与正常哺乳动物细胞中胱天蛋白酶的激活状态不同。与不直接诱导细胞死亡的靶向XIAP介导的caspase-9抑制的Smac肽相比,释放下游caspase而不是上游caspase可能是发现癌症药物的首选策略。

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