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通过胰岛素样生长因子受体1信号通路鉴定参与非小细胞肺癌吉非替尼耐药的微小RNA

Identification of microRNAs involved in gefitinib resistance of non-small-cell lung cancer through the insulin-like growth factor receptor 1 signaling pathway.

作者信息

Ma Wei, Kang Yanhong, Ning Lanlan, Tan Jie, Wang Hanping, Ying Yi

机构信息

Department of Respiration, Guangzhou First People's Hospital, Guangzhou, Guangdong 510180, P.R. China.

Department of Respiration, The First Affiliated Hospital/School of Clinical Medicine of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510000, P.R. China.

出版信息

Exp Ther Med. 2017 Oct;14(4):2853-2862. doi: 10.3892/etm.2017.4847. Epub 2017 Jul 28.

Abstract

Multiple clinical and experimental studies have suggested that epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) may be effective at treating advanced non-small cell lung cancer (NSCLC), however, the molecular basis of primary resistance to EGFR-TKIs in NSCLC remains unclear. In the current study, the insulin-like growth factor 1 receptor (IGF-1R) gene in the gefitinib-resistant human lung adenocarcinoma epithelial cell line A549 (A549/GR) was silenced using small interfering RNA (siRNA) in order to determine the role of microRNA (miRNA) in the development of resistance against epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in lung adenocarcinoma. The relative gefitinib-resistant capacity in A549 and A549/GR cells was determined using a cell counting kit 8. A549/GR cells were transfected with chemically synthesized siRNA to silence the IGF-1R gene. A total of 48 h after siRNA transfection, IGF-1R expression in A549/GR cells was evaluated using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and western blotting. miRNA expression in A549/GR cells and A549/GR cells with silenced IGF-1R was analyzed using a miRNA microarray. The microarray results of 10 miRNAs were then compared with the results of RT-qPCR. The results demonstrated that the gefitinib-resistance capacity of A549/GR cells was six times higher than that of A549 cells. Additionally, RT-qPCR and western blotting demonstrated that the IGF-1R gene in A549/GR cells was successfully silenced by siRNA. The highest silencing rate (72%) of the IGF-1R gene was obtained using siRNA-2. The microarray identified 72 miRNAs with significantly different expression in A549/GR cells with silenced IGF-1R compared with A549/GR cells. Of the 72 differentially expressed miRNAs, 13 miRNAs (including miR-497-3p and miR-1273c) were up-regulated and 59 miRNAs (including miR-361-3p and miR-345-3p) were down-regulated in A549/GR cells with silenced IGF-1R compared with A549/GR cells. The changes in the expression of 10 different miRNAs were confirmed by RT-qPCR. Thus, the present study successfully established an A549/GR cell line with silenced IGF-1R. The results suggest that a number of miRNAs associated with the IGF-1R signaling pathway, including miR-497-3p and miR-144-5p, were involved in the development of resistance against EGFR-TKIs in A549 cells. These miRNAs may provide novel targets to treat lung adenocarcinoma exhibiting resistance against EGFR-TKIs.

摘要

多项临床和实验研究表明,表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)可能对治疗晚期非小细胞肺癌(NSCLC)有效,然而,NSCLC对EGFR-TKIs原发性耐药的分子基础仍不清楚。在本研究中,使用小干扰RNA(siRNA)沉默了吉非替尼耐药的人肺腺癌上皮细胞系A549(A549/GR)中的胰岛素样生长因子1受体(IGF-1R)基因,以确定微小RNA(miRNA)在肺腺癌对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)耐药发展中的作用。使用细胞计数试剂盒8测定A549和A549/GR细胞中的相对吉非替尼耐药能力。用化学合成的siRNA转染A549/GR细胞以沉默IGF-1R基因。siRNA转染后共48小时,使用逆转录定量聚合酶链反应(RT-qPCR)和蛋白质印迹法评估A549/GR细胞中IGF-1R的表达。使用miRNA微阵列分析A549/GR细胞和IGF-1R沉默的A549/GR细胞中的miRNA表达。然后将10种miRNA的微阵列结果与RT-qPCR结果进行比较。结果表明,A549/GR细胞的吉非替尼耐药能力比A549细胞高6倍。此外,RT-qPCR和蛋白质印迹法表明,A549/GR细胞中的IGF-1R基因被siRNA成功沉默。使用siRNA-2获得了IGF-1R基因的最高沉默率(72%)。微阵列鉴定出72种miRNA在IGF-1R沉默的A549/GR细胞中与A549/GR细胞相比表达有显著差异。在这72种差异表达的miRNA中,与A549/GR细胞相比,13种miRNA(包括miR-497-3p和miR-1273c)在IGF-1R沉默的A549/GR细胞中上调,59种miRNA(包括miR-361-3p和miR-345-3p)下调。通过RT-qPCR证实了10种不同miRNA表达的变化。因此,本研究成功建立了IGF-1R沉默的A549/GR细胞系。结果表明,一些与IGF-1R信号通路相关的miRNA,包括miR-497-3p和miR-144-5p,参与了A549细胞对EGFR-TKIs耐药的发展。这些miRNA可能为治疗对EGFR-TKIs耐药的肺腺癌提供新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3326/5585727/3f4367fd6a2f/etm-14-04-2853-g00.jpg

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