Institute for Experimental Cancer Research in Pediatrics, Goethe-University Frankfurt, Komturstr. 3a, D-60528 Frankfurt/Main, Germany.
Department of Molecular and Clinical Cancer Medicine and Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Biol Chem. 2019 Jan 28;400(2):181-185. doi: 10.1515/hsz-2018-0233.
Induction of apoptosis by selective BH3-mimetics is currently investigated as a novel strategy for cancer treatment. Here, we report that selective BH3-mimetics induce apoptosis in a variety of hematological malignancies. Apoptosis is accompanied by severe mitochondrial toxicities upstream of caspase activation. Specifically, the selective BH3-mimetics ABT-199, A-1331852 and S63845, which target BCL-2, BCL-XL and MCL-1, respectively, induce comparable ultrastructural changes including mitochondrial swelling, a decrease of mitochondrial matrix density and severe loss of cristae structure. These shared effects on mitochondrial morphology indicate a similar function of these anti-apoptotic BCL-2 proteins in maintaining mitochondrial integrity and function.
诱导细胞凋亡是目前作为一种治疗癌症的新策略。在这里,我们报告说,选择性 BH3 模拟物可诱导多种血液系统恶性肿瘤细胞凋亡。凋亡伴随着 caspase 激活上游的严重线粒体毒性。具体来说,分别针对 BCL-2、BCL-XL 和 MCL-1 的选择性 BH3 模拟物 ABT-199、A-1331852 和 S63845 诱导相似的超微结构变化,包括线粒体肿胀、线粒体基质密度降低和嵴结构严重缺失。这些在线粒体形态上的相似作用表明这些抗凋亡 BCL-2 蛋白在维持线粒体完整性和功能方面具有相似的功能。