A patent review of small molecule CDK4/6 inhibitors in the treatment of cancer: 2020–present

激酶 癌症 丝氨酸 肺癌 细胞周期蛋白依赖激酶 细胞周期蛋白依赖激酶4 药理学 医学 蛋白激酶A 癌症研究 细胞周期 化学 生物 细胞周期蛋白依赖激酶2 磷酸化 肿瘤科 生物化学 遗传学
作者
Xiaoling Huang,Shidi Xu,Shidi Xu,Lei Duan,Shan Xu,Shan Xu,Wufu Zhu
出处
期刊:Expert Opinion on Therapeutic Patents [Taylor & Francis]
卷期号:34 (9): 825-842 被引量:6
标识
DOI:10.1080/13543776.2024.2379926
摘要

INTRODUCTION: Cyclin-dependent protein kinase 4/6 (CDK4/6) is a class of serine/threonine protein kinases that plays a key role in the regulation of the cell cycle. CDK4/6 is highly expressed in cancers such as breast cancer, melanoma, and non-small cell lung cancer (NSCLC). Currently, a variety of CDK4/6 inhibitors have been developed, aiming to develop effective inhibitors to solve CDK4/6 resistance and toxicity. AREAS COVERED: This article searches patents through Espacenet and reviews the development of widely studied CDK inhibitors and FDA-approved CDK4/6 inhibitors, as well as the latest progress of patented inhibitors with good inhibitory activity against CDK4/6 from 2020 to now. EXPERT OPINION: CDK4/6 is highly expressed in many tumors and has become an important anti-tumor target. Among the patents from 2020 to the present, many inhibitors have good kinase inhibitory effects on CDK4/6 and also show great development potential in anti-tumor. However, there is still an urgent need to develop novel CDK4/6 inhibitors that address challenges such as drug resistance, toxicity, and selectivity.
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