State Key Laboratory of Biotherapy and Cancer Center and Department of Orthopedics, and Department of Otolaryngology, Head and Neck Surgery, West China Hospital, Sichuan University, Chengdu 610041, China.
J Med Chem. 2022 Feb 24;65(4):2989-3001. doi: 10.1021/acs.jmedchem.1c01572. Epub 2022 Feb 7.
Regulated cell death is a widely attractive subject among the topics of cancer therapy and has gained some advances for discovery of targeted anticancer drugs. In the past decade, nonapoptotic regulated cell death has been implicated in the development and therapeutic responses of a variety of human cancers. Hitherto, targeting autophagy-dependent cell death (ADCD), ferroptosis, and necroptosis with small molecules has been emerging as a hopeful strategy for the improvement of potential cancer therapy, which may have an advantage to bypass the apoptosis-resistance machinery. Thus, in this perspective, we concentrate on the key molecular insights into ADCD, ferroptosis, and necroptosis and summarize the corresponding small molecules in potential cancer therapy. Moreover, the relationships between the three subroutines and small molecules modulating the crosstalk are discussed. We believe that these inspiring findings would be advantageous to exploiting more potential targets and pharmacological small molecules in future cancer treatment.
细胞程序性死亡是癌症治疗领域中一个备受关注的课题,在发现针对癌症的靶向药物方面取得了一些进展。在过去的十年中,非凋亡性细胞程序性死亡已被证实与多种人类癌症的发生和治疗反应有关。迄今为止,用小分子靶向自噬依赖性细胞死亡(ADCD)、铁死亡和坏死性细胞死亡已成为提高潜在癌症治疗效果的一种有希望的策略,这可能有助于绕过细胞凋亡抵抗机制。因此,在这篇观点文章中,我们集中讨论 ADCD、铁死亡和坏死性细胞死亡的关键分子见解,并总结潜在癌症治疗中相应的小分子。此外,还讨论了三种子程序和调节细胞间串扰的小分子之间的关系。我们相信,这些令人鼓舞的发现将有助于在未来的癌症治疗中开发更多的潜在靶点和药理学小分子。