Research Centre of Siyuan Natural Pharmacy and Biotoxicology, College of Life Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China; Joint Centre of Zhejiang University and the Chinese University of Hong Kong on Natural Products and Toxicology Research, Zhejiang University, Hangzhou, People's Republic of China.
Research Centre of Siyuan Natural Pharmacy and Biotoxicology, College of Life Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China; Joint Centre of Zhejiang University and the Chinese University of Hong Kong on Natural Products and Toxicology Research, Zhejiang University, Hangzhou, People's Republic of China.
Biochem Biophys Res Commun. 2021 Aug 27;567:22-28. doi: 10.1016/j.bbrc.2021.05.103. Epub 2021 Jun 13.
ABT-737, a small molecule BH-3 mimetic, is less effective against human colon cancers due to its resistance. Verticillin A is a natural compound, which was previously purified from verticillium-infected mushrooms. Hence, we aimed at overcoming the ABT737 resistance observed in CRC tumors by combining Verticillin A with ABT-737 and figuring out the potential mechanism. In this study, we observed that Verticillin A could sensitize colon cancer to ABT-737-induced cell death through induction of mitochondrial-dependent apoptosis. Verticillin A could significantly increase the BIMEL/MCL-1 ratio to overcome ABT737 resistance through the suppression of the MEK/ERK pathway. In addition, up-regulation of BIM protein levels to activate BAX translocation results in apoptosis induction. Altogether, our work suggested the potential application of Verticillin A as a MEK inhibitor in BH3-mimetic-based therapy.
ABT-737 是一种小分子 BH3 模拟物,由于其耐药性,对人类结肠癌的疗效较差。Verticillin A 是一种天然化合物,以前从感染 verticillium 的蘑菇中纯化出来。因此,我们旨在通过将 Verticillin A 与 ABT-737 联合使用来克服 CRC 肿瘤中观察到的 ABT737 耐药性,并研究其潜在机制。在这项研究中,我们观察到 Verticillin A 通过诱导线粒体依赖性细胞凋亡使结肠癌对 ABT-737 诱导的细胞死亡敏感。Verticillin A 通过抑制 MEK/ERK 通路显著增加 BIMEL/MCL-1 比值,从而克服 ABT737 耐药性。此外,上调 BIM 蛋白水平以激活 BAX 易位导致凋亡诱导。总的来说,我们的工作表明 Verticillin A 作为一种 MEK 抑制剂在基于 BH3 模拟物的治疗中具有潜在的应用价值。