Preclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Cells. 2020 May 21;9(5):1287. doi: 10.3390/cells9051287.
The dynamic interplay between pro-death and pro-survival Bcl-2 family proteins is responsible for a cell's fate. Due to the recognized relevance of this family in cancer progression and response to therapy, different efforts have made in recent years in order to develop small molecules able to target anti-apoptotic proteins such as Bcl-2, Bcl-xL and Mcl-1. The limitations of the first Bcl-2 family targeted drugs, regarding on-target and off-target toxicities, have been overcome with the development of venetoclax (ABT-199), the first BH3 mimetic inhibitor approved by the FDA. The purpose of this review is to discuss the state-of-the-art in the development of drugs targeting Bcl-2 anti-apoptotic proteins and to highlight the potential of their application as single agents or in combination for improving anti-cancer therapy, focusing in particular on solid tumors.
促死亡和抗生存 Bcl-2 家族蛋白之间的动态相互作用决定了细胞的命运。由于该家族在癌症进展和对治疗的反应中的相关性已得到公认,近年来人们做出了不同的努力,以开发能够靶向抗凋亡蛋白(如 Bcl-2、Bcl-xL 和 Mcl-1)的小分子。由于第一代 Bcl-2 家族靶向药物存在针对靶标和非靶标毒性的限制,因此 Venetoclax(ABT-199)的开发已经克服了这些限制,Venetoclax 是第一个获得 FDA 批准的 BH3 模拟抑制剂。本文的目的是讨论针对 Bcl-2 抗凋亡蛋白的药物开发的最新进展,并强调它们作为单一药物或联合应用在改善癌症治疗中的潜力,特别是针对实体瘤。