Department of Thoracic Surgery, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Eur Rev Med Pharmacol Sci. 2019 Mar;23(6):2444-2452. doi: 10.26355/eurrev_201903_17391.
To clarify the function of miRNA-153-3p in gefitinib-sensitive non-small cell lung cancer (NSCLC) and the underlying mechanism.
The expressions of miRNA-153-3p, LC3B and ATG5 in gefitinib-resistant and gefitinib-sensitive NSCLC tissues were determined by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). The correlation between miRNA-153-3p to LC3B or ATG5 was analyzed. We evaluated autophagy level in gefitinib-resistant NSCLC cells by calculating the percentage of PC-9/GR and HCC827/GR cells with positive GFP-LC3, as well as determining autophagy-related gene levels. The potential binding between ATG5 and miRNA-153-3p were verified by Dual-Luciferase reporter gene assay. The regulatory effects of miRNA-153-3p/ATG5 on gefitinib-sensitivity and apoptosis were finally examined by cytotoxicity assay and Annexin V-fluorescein isothiocyanate (FITC)/Propidium Iodide (PI) staining, respectively.
MiRNA-153-3p was lowly expressed in gefitinib-resistant NSCLC relative to the gefitinib-sensitive ones. MiRNA-153-3p was negatively correlated with autophagy activity marker LC3B in gefitinib-resistant NSCLC patients. Compared with parental cells, gefitinib-resistant NSCLC cell lines PC-9/GR and HCC827/GR presented a lower level of miRNA-153-3p and a higher level of autophagy. The overexpression of miRNA-153-3p greatly inhibited autophagy level. ATG5 could directly bind to miRNA-153-3p, and ATG5 was highly expressed in gefitinib-resistant NSCLC. The correlation analysis found a negative correlation between ATG5 and miRNA-153-3p and a positive correlation between ATG5 and LC3B in gefitinib-resistant NSCLC. More importantly, ATG5 reversed the regulatory effects of miRNA-153-3p on autophagy, gefitinib-sensitivity and apoptosis of PC-9/GR and HCC827/GR cells.
MiRNA-153-3p is lowly expressed in gefitinib-resistant NSCLC patients. The overexpression of miRNA-153-3p enhances gefitinib-sensitivity in NSCLC by inhibiting autophagy via downregulating ATG5.
阐明 miRNA-153-3p 在吉非替尼敏感的非小细胞肺癌(NSCLC)中的作用及其潜在机制。
采用实时定量聚合酶链反应(qRT-PCR)检测吉非替尼耐药和吉非替尼敏感的 NSCLC 组织中 miRNA-153-3p、LC3B 和 ATG5 的表达,分析 miRNA-153-3p 与 LC3B 或 ATG5 的相关性。通过计算 PC-9/GR 和 HCC827/GR 细胞中 GFP-LC3 阳性细胞的百分比以及检测自噬相关基因水平,评估吉非替尼耐药 NSCLC 细胞中的自噬水平。采用双荧光素酶报告基因检测验证 ATG5 与 miRNA-153-3p 的潜在结合。最后通过细胞毒性测定和 Annexin V-荧光素异硫氰酸酯(FITC)/碘化丙啶(PI)染色分别检测 miRNA-153-3p/ATG5 对吉非替尼敏感性和细胞凋亡的调控作用。
miRNA-153-3p 在吉非替尼耐药 NSCLC 组织中表达水平低于吉非替尼敏感组织。miRNA-153-3p 与吉非替尼耐药 NSCLC 患者的自噬活性标志物 LC3B 呈负相关。与亲本细胞相比,吉非替尼耐药 NSCLC 细胞系 PC-9/GR 和 HCC827/GR 细胞中 miRNA-153-3p 表达水平较低,自噬水平较高。miRNA-153-3p 的过表达可显著抑制自噬水平。ATG5 可直接与 miRNA-153-3p 结合,且在吉非替尼耐药 NSCLC 中高表达。相关性分析发现,在吉非替尼耐药 NSCLC 中,ATG5 与 miRNA-153-3p 呈负相关,与 LC3B 呈正相关。更为重要的是,ATG5 逆转了 miRNA-153-3p 对 PC-9/GR 和 HCC827/GR 细胞自噬、吉非替尼敏感性和细胞凋亡的调节作用。
miRNA-153-3p 在吉非替尼耐药 NSCLC 患者中低表达。过表达 miRNA-153-3p 通过下调 ATG5 抑制自噬,增强 NSCLC 对吉非替尼的敏感性。