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How to unleash mitochondrial apoptotic blockades to kill cancers?

机译:如何释放线粒体的凋亡阻滞来杀死癌症?

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摘要

Apoptosis, especially the intrinsic mitochondrial cell death pathway, is regulated by the BCL-2 family of proteins. Defects in apoptotic machinery are one of the main mechanisms that cells employ to evade cell death and become cancerous. Targeting the apoptotic defects, either by direct inhibition of BCL-2 family proteins or through modulation of regulatory pathways, can restore cell sensitivity to cell death. This review will focus on the aspects of BCL-2 family proteins, their interactions with kinase pathways, and how novel targeted agents can help overcome the apoptotic blockades. Furthermore, functional assays, such as BH3 profiling, may help in predicting responses to chemotherapies and aid in the selection of combination therapies by determining the mitochondrial threshold for initiating cell death.
机译:凋亡,尤其是固有的线粒体细胞死亡途径,受BCL-2家族的蛋白质调控。凋亡机制中的缺陷是细胞用来逃避细胞死亡并变成癌症的主要机制之一。通过直接抑制BCL-2家族蛋白或通过调节调节途径来靶向凋亡缺陷,可以恢复细胞对细胞死亡的敏感性。这篇综述将侧重于BCL-2家族蛋白,它们与激酶途径的相互作用以及新型靶向药物如何帮助克服细胞凋亡阻滞的方面。此外,功能测定(例如BH3分析)可能有助于确定对化学疗法的反应,并通过确定引发细胞死亡的线粒体阈值来帮助选择联合疗法。

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