Ye Qingmei, Zhuang Xiao-Zhao, Li Juan, Zhou Xin
Hainan General Hospital and Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, China.
Hubei Province Key Laboratory of Traditional Chinese Medicine Resource and Chemistry, Department of Pharmacy, Hubei University of Chinese Medicine, Wuhan, Hubei, China.
Front Pharmacol. 2025 Mar 28;16:1562167. doi: 10.3389/fphar.2025.1562167. eCollection 2025.
Inhibitors of Apoptosis Proteins (IAPs) are a family of anti-apoptotic proteins that play a pivotal role in apoptosis in general but also as oncoproteins in cancer progression and, more importantly, drug resistance. IAPs enable cancer cells to evade programmed cell death and adapt to therapeutic stress by inhibiting pro-apoptotic caspase activity as well as modulating pivotal survival pathways. Recent advancements in targeting IAPs, particularly through the use of SMAC (second mitochondria-derived activator of caspase) mimetics and other small-molecule antagonists or inhibitors, have opened new avenues for overcoming drug resistance in cancers. The current review attempted to summarize the of IAPs' role in promoting chemotherapeutic drug resistance in various cancer treatments and discuss the most recent development of IAP-targeting therapies, particularly small-molecule inhibitors including their combinational strategies to enhance the sensitivity or achieve synergism to existing therapeutics. Additionally, we also outline the challenges and offer future perspectives for optimizing IAP-targeted approaches to improve clinical outcomes.
凋亡抑制蛋白(IAPs)是一类抗凋亡蛋白,它们在一般的细胞凋亡中起着关键作用,但在癌症进展中作为癌蛋白,更重要的是在耐药性方面也发挥着作用。IAPs通过抑制促凋亡半胱天冬酶活性以及调节关键的生存途径,使癌细胞能够逃避程序性细胞死亡并适应治疗压力。靶向IAPs的最新进展,特别是通过使用SMAC(线粒体衍生的半胱天冬酶激活剂-2)模拟物和其他小分子拮抗剂或抑制剂,为克服癌症耐药性开辟了新途径。本综述试图总结IAPs在各种癌症治疗中促进化疗耐药性的作用,并讨论靶向IAPs疗法的最新进展,特别是小分子抑制剂,包括它们的联合策略,以提高对现有疗法的敏感性或实现协同作用。此外,我们还概述了挑战,并为优化靶向IAPs的方法以改善临床结果提供了未来展望。