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抑制 Sevenless 同源物 1(SOS1):治疗 KRAS 突变型癌症的有前景的治疗方法。

Inhibition of Son of Sevenless Homologue 1 (SOS1): Promising therapeutic treatment for KRAS-mutant cancers.

机构信息

School of Pharmacy, China Pharmaceutical University, Nanjing, 211198, People's Republic of China.

School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, People's Republic of China.

出版信息

Eur J Med Chem. 2023 Dec 5;261:115828. doi: 10.1016/j.ejmech.2023.115828. Epub 2023 Sep 25.

Abstract

Kristen rat sarcoma (KRAS) is one of the most common oncogenes in human cancers. As a guanine nucleotide exchange factor, Son of Sevenless Homologue 1 (SOS1) represents a potential therapeutic concept for the treatment of KRAS-mutant cancers because of its activation on KRAS and downstream signaling pathways. In this review, we provide a comprehensive overview of the structure, biological function, and regulation of SOS1. We also focus on the recent advances in SOS1 inhibitors and emphasize their binding modes, structure-activity relationships and pharmacological activities. We hope that this publication can provide a comprehensive compendium on the rational design of SOS1 inhibitors.

摘要

KRAS 是人类癌症中最常见的致癌基因之一。作为鸟嘌呤核苷酸交换因子,SOS1 代表了治疗 KRAS 突变型癌症的潜在治疗概念,因为它能激活 KRAS 和下游信号通路。在这篇综述中,我们全面概述了 SOS1 的结构、生物学功能和调节。我们还重点介绍了 SOS1 抑制剂的最新进展,并强调了它们的结合模式、构效关系和药理活性。我们希望本出版物能为 SOS1 抑制剂的合理设计提供一个全面的纲要。

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