Zhou Yang, Xiang Shuang, Yang Fang, Lu Xiaoyun
International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Discovery of Chinese Ministry of Education (MOE), School of Pharmacy, Jinan University, 855 Xingye Avenue, Guangzhou 510632, China.
J Med Chem. 2022 Dec 8;65(23):15540-15558. doi: 10.1021/acs.jmedchem.2c01361. Epub 2022 Nov 17.
Clinically acquired resistance is a major challenge in cancer therapies with small-molecule kinase inhibitors (SMKIs). Gatekeeper mutations in the ATP-binding pocket of kinases are the most common mutations leading to acquired resistance. To date, seven new-generation kinase inhibitors targeting gatekeeper mutations have been approved by the FDA; however, the clinical need is still unmet. Here, we systematically summarize the types of gatekeeper mutations across the kinase family, the structural basis for acquired resistance, and newly developed SMKIs targeting gatekeeper mutations as well as highlight the opportunities and challenges of kinase drug discovery for targeting gatekeeper mutations.
临床获得性耐药是小分子激酶抑制剂(SMKIs)癌症治疗中的一个主要挑战。激酶ATP结合口袋中的守门人突变是导致获得性耐药的最常见突变。迄今为止,美国食品药品监督管理局(FDA)已批准了七种针对守门人突变的新一代激酶抑制剂;然而,临床需求仍未得到满足。在这里,我们系统地总结了整个激酶家族中守门人突变的类型、获得性耐药的结构基础、新开发的针对守门人突变的SMKIs,并强调了针对守门人突变进行激酶药物研发的机遇和挑战。