School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai, 200433, PR China; School of Health Sciences and Engineering, University of Shanghai for Science and Technology, Shanghai, 200093, PR China.
School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai, 200433, PR China; 92805 Military Hospital, Qingdao, PR China.
Eur J Med Chem. 2024 Dec 5;279:116878. doi: 10.1016/j.ejmech.2024.116878. Epub 2024 Sep 19.
Peptides represent attractive molecules for targeting protein-protein interactions, and peptide drug development has made great progress during the last decades. Ras protein, the most promising target in cancer therapy, is one of the major growth drivers in various cancers. Although many small molecule inhibitors have been reported to effectively target Ras protein and some inhibitors (such as MRTX849 and AMG 510) have been translated into clinical application, just a few peptide inhibitors have been reported. Here we summarize different types of peptide inhibitors, including monocyclic peptides, bicyclic peptides, stapled peptides, and proteomimetic inhibitors, developed in recent years; emphasize the limits and achievements; and discuss the outlook and challenges associated with future research in peptide inhibitors. This review aims to provide a reference for the discovery of Ras peptide inhibitors.
肽是靶向蛋白-蛋白相互作用的有吸引力的分子,肽类药物的开发在过去几十年中取得了巨大进展。Ras 蛋白是癌症治疗中最有希望的靶点之一,是各种癌症中主要的生长驱动因子之一。尽管已经报道了许多小分子抑制剂可以有效地靶向 Ras 蛋白,并且一些抑制剂(如 MRTX849 和 AMG510)已转化为临床应用,但仅报道了少数肽抑制剂。在这里,我们总结了近年来开发的不同类型的肽抑制剂,包括单环肽、双环肽、订书肽和拟肽抑制剂;强调了它们的局限性和成就;并讨论了与未来肽抑制剂研究相关的展望和挑战。本文旨在为 Ras 肽抑制剂的发现提供参考。