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miRNA-153-3p 通过抑制 ATG5 表达和自噬来促进非小细胞肺癌对吉非替尼的敏感性。

MiRNA-153-3p promotes gefitinib-sensitivity in non-small cell lung cancer by inhibiting ATG5 expression and autophagy.

机构信息

Department of Thoracic Surgery, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Mar;23(6):2444-2452. doi: 10.26355/eurrev_201903_17391.

Abstract

OBJECTIVE

To clarify the function of miRNA-153-3p in gefitinib-sensitive non-small cell lung cancer (NSCLC) and the underlying mechanism.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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