吉非替尼
奥西默替尼
表皮生长因子受体
癌症研究
肺癌
酪氨酸激酶
埃罗替尼
生物
癌基因
医学
表皮生长因子
癌症
细胞培养
肿瘤科
受体
内科学
细胞周期
遗传学
作者
Alessia Belloni,Armanda Pugnaloni,Maria Rita Rippo,Silvia Di Valerio,Chiara Giordani,Antonio Domenico Procopio,Giuseppe Bronte
标识
DOI:10.1016/j.critrevonc.2023.104246
摘要
Non-Small Cell Lung Cancer (NSCLC) represents ~85% of all lung cancers and ~15-20% of them are characterized by mutations affecting the Epidermal Growth Factor Receptor (EGFR). For several years now, a class of tyrosine kinase inhibitors was developed, targeting sensitive mutations affecting the EGFR (EGFR-TKIs). To date, the main burden of the TKIs employment is due to the onset of resistance mutations. This scoping review aims to resume the current situation about the cell line models employed for the in vitro evaluation of resistance mechanisms induced by EGFR-TKIs in oncogene-addicted NSCLC. Adenocarcinoma results the most studied NSCLC histotype with the H1650, H1975, HCC827 and PC9 mutated cell lines, while Gefitinib and Osimertinib the most investigated inhibitors. Overall, data collected frame the current advancement of this topic, showing a plethora of approaches pursued to overcome the TKIs resistance, from RNA-mediated strategies to the innovative combination therapies.
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