高蕊, 冯帆, 贾辉, 张帆, 王涛, 董国福, 马德宾, 马宏达, 韩雅玲, 刘蕾. miRNA153反义核酸上调肺癌细胞对辐射敏感性的体外实验[J]. 解放军医学院学报, 2015, 36(10): 1033-1038. DOI: 10.3969/j.issn.2095-5227.2015.10.019
引用本文: 高蕊, 冯帆, 贾辉, 张帆, 王涛, 董国福, 马德宾, 马宏达, 韩雅玲, 刘蕾. miRNA153反义核酸上调肺癌细胞对辐射敏感性的体外实验[J]. 解放军医学院学报, 2015, 36(10): 1033-1038. DOI: 10.3969/j.issn.2095-5227.2015.10.019
GAO Rui, FENG Fan, JIA Hui, ZHANG Fan, WANG Tao, DONG Guofu, MA Debin, MA Hongda, HAN Yaling, LIU Lei. Up-regulation of microRNA153 causes radio-sensitization of lung cancer cells in vitro experiments[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2015, 36(10): 1033-1038. DOI: 10.3969/j.issn.2095-5227.2015.10.019
Citation: GAO Rui, FENG Fan, JIA Hui, ZHANG Fan, WANG Tao, DONG Guofu, MA Debin, MA Hongda, HAN Yaling, LIU Lei. Up-regulation of microRNA153 causes radio-sensitization of lung cancer cells in vitro experiments[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2015, 36(10): 1033-1038. DOI: 10.3969/j.issn.2095-5227.2015.10.019

miRNA153反义核酸上调肺癌细胞对辐射敏感性的体外实验

Up-regulation of microRNA153 causes radio-sensitization of lung cancer cells in vitro experiments

  • 摘要: 目的 探讨反义核酸沉默microRNA 153(miRNA153)对电离辐射杀伤肺癌细胞株的影响。 方法 利用脂质体转染miRNA153的反义核酸;使用60Co-γ射线照射肺癌细胞;使用CCK-8实验、软琼脂成集落实验(锚定非依赖性生长)和Trans-well实验检测miRNA153反义核酸对电离辐射杀伤肺癌细胞的影响;RT-PCR和Western blot实验检测miRNA153的反义核酸对miRNA153、其靶标蛋白PTEN以及细胞存活/凋亡耐受调控蛋白Survivin表达的影响。 结果 CCK-8实验结果显示,中等剂量射线(4 Gy)照射能够杀伤肺癌细胞A549、H460、H1299和H358,下调miRNA153的表达能够增强辐射对肺癌细胞的杀伤作用;软琼脂成集落和Transwell实验进一步证实miRNA153的反义核酸能够上调辐射对A549细胞锚定非依赖性生长和侵袭的抑制作用。分子机制实验结果表明,miRNA153的反义核酸能够显著降低miRNA153的表达水平,提高肿瘤抑制因子PTEN并降低细胞存活因子Survivin的表达。 结论 降低miRNA153的表达能够上调辐射对肺癌细胞系的体外杀伤作用。

     

    Abstract: Objective To declare whether silencing of miRNA153 via its anti-sense nuclear (inhibitor) induces the radio-sensitization of lung cancer cells. Methods The anti-sense nuclear acid (inhibitor) of miRNA153 was transfected into lung cancer cells, which were irradiated by 60Co-γ. The CCK-8 analysis, soft-agar and Transwell assays were performed to identify the effect of miRNA153 silencing on radio-sensitization in lung cancer cells. RT-PCR and Western blot assays were used to detect the effect of anti-sense nuclear acid (inhibitor) of miRNA153 on miRNA153, its target protein PTEN and the expression of Survivin cell proliferation of survival regulators. Results CCK-8 analysis revealed that the irradiation of medium dose ray (4 Gy) could kill the lung cancer cells (A549, H460, H1299 and H358), and the down-regulation of expression of miRNA153 could enhance the radio-sensitization in lung cancer cells. The soft-agar and Transwell assays proved that the up-regulation of rays could inhibit the anchorage-independent growth and invasion of A549 cells. And the molecular mechanism experiment indicated that the anti-sense nuclear acid of miRNA153 significantly disrupted the endogenous expression of miRNA153 and Survivin, and in turn upregulated the expression of PTEN. Conclusion Silencing of miR-153 significantly enhances the sensitivity of lung cancers.

     

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