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Molecular mechanism of acquired drug resistance in the EGFR‐TKI resistant cell line HCC827‐TR

机译:EGFR-TKI抗性细胞系HCC827-TR中获得耐药性的分子机制

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BACKGROUND:The first-line standard treatment of non-small cell lung cancer (NSCLC) with EGFR mutation is EGFR-tyrosine kinase inhibitors (TKIs). However, most patients will develop acquired resistance after 9-13?months. This study investigated novel molecular mechanisms of acquired resistance to EGFR-TKIs to identify a potential new treatment for EGFR-TKI resistant NSCLC patients.METHODS:We established an EGFR-TKI resistant cell line (HCC827-TR) by culturing the HCC827-P cell line through continuous erlotinib culture. We used Sanger sequencing, RT-PCR, and western blot to rule out known resistance mechanisms in HCC827-TR cells, including EGFR-T790M and MET, PTEN, or EGFR expression changes. Next-generation sequencing was performed and identified differentially expressed genes between two cell lines and examined the genes with GO and KEGG pathway database analyses. We also examined the molecular alterations in COSMIC and GDSC databases and performed hazard predictions using SIFT, PolyPhen-2, Mutation Taster, and CADD.RESULTS:Our results identified FGF2 as a differentially expressed gene with a G101T point mutation in HCC827-TR cells that showed high mutation frequency and hazard score. HCC827-TR cells showed elevated FGF2 compared to parental cells. It is noteworthy that treatment with the FGFR inhibitor AZD4547 could restore the sensitivity of HCC872-TR cells to erlotinib.CONCLUSIONS:An erlotinib-resistant cell line HCC827-TR was successfully constructed and we identified the EGFR-TKI resistance mechanism involving the FGF2 gene mutation. Targeted inhibition of the FGF2/FGFR signaling pathway may effectively restore the sensitivity of the resistant cells to erlotinib. These results suggest a novel treatment strategy for EGFR-TKI resistant NSCLC patients.KEY POINTS:Significant findings of the study: Identifies a novel molecular mechanism for EGFR-TKI acquired resistance.WHAT THIS STUDY ADDS:A potential novel strategy for the treatment of EGFR-TKI resistant NSCLC patients.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:具有EGFR突变的非小细胞肺癌(NSCLC)的第一线标准治疗是EGFR-酪氨酸激酶抑制剂(TKI)。然而,大多数患者将在9-13个月后发育获得的抵抗力。本研究研究了对EGFR-TKI的获得性抗性的新分子机制,以鉴定EGFR-TKI抗性NSCLC患者的潜在新治疗方法。方法:通过培养HCC827-P细胞建立了EGFR-TKI抗性细胞系(HCC827-TR)通过连续的orlotinib培养线。我们使用Sanger测序,RT-PCR和Western Blot来排除HCC827-TR细胞中的已知电阻机制,包括EGFR-T790M并满足,PTEN或EGFR表达变化。进行下一代测序并鉴定两种细胞系之间的差异表达基因,并通过GO和KEGG途径数据库分析检查基因。我们还检查了宇宙和GDSC数据库中的分子改变,并使用Sift,Polyphen-2,突变捷体和CADD进行危害预测。结果:我们的结果将FGF2鉴定为差异表达的基因,HCC827-TR细胞中的G101T点突变显示出高突变频率和危险评分。与父母细胞相比,HCC827-TR细胞显示出升高的FGF2。值得注意的是,使用FGFR抑制剂AZD4547的治疗可以将HCC872-TR细胞的敏感性恢复为erlotinib.COLLOTINIB耐药细胞系HCC827-TR,并确定了涉及FGF2基因突变的EGFR-TKI抗性机制。针对FGF2 / FGFR信号通路的靶向抑制可以有效地将抗性细胞的敏感性恢复到厄洛替尼。这些结果表明了EGFR-TKI抗性NSCLC患者的新型治疗策略。表现:研究的重要发现:鉴定EGFR-TKI获得性的新型分子机制。本研究补充说:潜在的新策略,用于治疗EGFR的潜在新策略-TKI抗性NSCLC患者。? 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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