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Combined FGFR and Akt pathway inhibition abrogates growth of FGFR1 overexpressing EGFR-TKI-resistant NSCLC cells

机译:结合FGFR和AKT途径抑制废除过表达EGFR-TKI抗性NSCLC细胞的FGFR1生长

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摘要

a Tolerance to erlotinib and afatinib was assessed in the parental HCC827 and the three erlotinib-resistant cell lines, ER10, ER20, and ER30, by crystal violet assay after 72 h incubation. Data are presented as the average of four replicates and shown as mean ± SD. b Selected proteins significantly regulated across the three erlotinib-resistant cell lines compared to the parental HCC827, as assessed by mass spectrometry-based proteomics, were classified according to function. The dotted red line indicates 2-fold regulation. c Western blot analysis of total and phosphorylated levels of selected signaling proteins. The HCC827 cell lines were exposed to erlotinib (30 µM) for 4 h, the ER10, ER20, and ER30 samples without erlotinib were grown 24 h in the absence of erlotinib, while ER10, ER20, and ER30 samples with erlotinib were grown in media containing 10, 20, and 30 µM erlotinib, respectively, before being harvested for the western blotting in (c).
机译:通过在72小时孵育后,在亲本HCC827和三种替代抗性细胞系,ER10,ER20和ER30中评估对厄洛替尼和AFATINIB的耐受性。数据显示为四个重复的平均值,并显示为平均值±SD。 B根据功能评估,与亲本HCC827相比,与亲本HCC827相比,在三个替替尼抗性细胞系上显着调节的选定蛋白质根据功能进行分类。虚线红线表示2倍调节。 C类别和磷酸化水平的Cestern印迹分析。将HCC827细胞系暴露于厄洛替尼(30μm),4小时,ER10,ER20和ER30在没有Erlotinib的情况下生长24小时,而ER10,ER20和ER30在培养基中生长欧洲毒素分别含有10,20和30μm的欧洛替尼,然后在(c)中被收获以进行蛋白质印迹。

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