表皮生长因子受体
靶向治疗
肺癌
吉非替尼
抗药性
医学
癌症研究
酪氨酸激酶
埃罗替尼
表皮生长因子受体抑制剂
癌症
药品
生物
肿瘤科
受体
药理学
内科学
遗传学
作者
Houssein Chhouri,David Alexandre,Luca Grumolato
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2023-01-13
卷期号:15 (2): 504-504
被引量:93
标识
DOI:10.3390/cancers15020504
摘要
Non-small cell lung cancers (NSCLC) harboring activating mutations of the epidermal growth factor receptor (EGFR) are treated with specific tyrosine kinase inhibitors (EGFR-TKIs) of this receptor, resulting in clinically responses that can generally last several months. Unfortunately, EGFR-targeted therapy also favors the emergence of drug tolerant or resistant cells, ultimately resulting in tumor relapse. Recently, cellular barcoding strategies have arisen as a powerful tool to investigate the clonal evolution of these subpopulations in response to anti-cancer drugs. In this review, we provide an overview of the currently available treatment options for NSCLC, focusing on EGFR targeted therapy, and discuss the common mechanisms of resistance to EGFR-TKIs. We also review the characteristics of drug-tolerant persister (DTP) cells and the mechanistic basis of drug tolerance in EGFR-mutant NSCLC. Lastly, we address how cellular barcoding can be applied to investigate the response and the behavior of DTP cells upon EGFR-TKI treatment.
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