ROS1型
肺癌
医学
激酶
癌症研究
靶向治疗
癌症
间变性淋巴瘤激酶
非小细胞肺癌
肿瘤科
内科学
生物信息学
腺癌
生物
细胞生物学
A549电池
恶性胸腔积液
作者
Debasis Das,Jingbing Wang,Hong Jian
出处
期刊:ChemMedChem
[Wiley]
日期:2021-04-30
卷期号:16 (16): 2459-2479
被引量:30
标识
DOI:10.1002/cmdc.202100166
摘要
Lung cancer causes many deaths globally. Mutations in regulatory genes, irregularities in specific signal transduction events, or alterations of signalling pathways are observed in cases of non-small cell lung cancer (NSCLC). Over the past two decades, a few kinases have been identified, validated, and studied as biomarkers for NSCLC. Among them, EGFR, ALK, ROS1, MET, RET, NTRK, and BRAF are regarded as targetable biomarkers to cure and/or control the disease. In recent years, the US Food and Drug Administration (FDA) approved more than 15 kinase inhibitors targeting these NSCLC biomarkers. The kinase inhibitors significantly improved the progression-free survival (PFS) of NSCLC patients. Challenges still remain for metastatic diseases and advanced NSCLC cases. New discoveries of potent kinase inhibitors and rapid development of modern medical technologies will help to control NSCLC cases. This article provides an overview of the discoveries of various types of kinase inhibitors against NSCLC, along with medicinal chemistry aspects and related developments in next-generation kinase inhibitors that have been reported in recent years.
科研通智能强力驱动
Strongly Powered by AbleSci AI