miR-216a-5p inhibits invasion ability in human lung cancer cells by down-regulation of MMP16 expression

安　宁; 李宏敏; 于瑞莲

doi:10.3969/j.issn.1007-3969.2015.08.005

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miR-216a-5p inhibits invasion ability in human lung cancer cells by down-regulation of MMP16 expression

更新时间：2025-12-31

- miR-216a-5p inhibits invasion ability in human lung cancer cells by down-regulation of MMP16 expression
- China Oncology Vol. 25, Issue 8, Pages: 588-594(2015)
- 作者机构：
  
  四川省医学科学院，四川省人民医院肿瘤科,四川,成都,610072
- 作者简介：
- 基金信息：
- DOI：10.3969/j.issn.1007-3969.2015.08.005
  CLC：
- Published Online：14 December 2015，
  
  Published：14 December 2015
- 稿件说明：
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安　宁,李宏敏,于瑞莲,等. miR-216a-5p通过下调MMP16表达抑制肺癌细胞的侵袭[J]. 中国癌症杂志, 2015, 25(8): 588-594.

安　宁, 李宏敏, 于瑞莲. miR-216a-5p inhibits invasion ability in human lung cancer cells by down-regulation of MMP16 expression[J]. China Oncology, 2015, 25(8): 588-594.
安　宁,李宏敏,于瑞莲,等. miR-216a-5p通过下调MMP16表达抑制肺癌细胞的侵袭[J]. 中国癌症杂志, 2015, 25(8): 588-594. DOI： 10.3969/j.issn.1007-3969.2015.08.005.

安　宁, 李宏敏, 于瑞莲. miR-216a-5p inhibits invasion ability in human lung cancer cells by down-regulation of MMP16 expression[J]. China Oncology, 2015, 25(8): 588-594. DOI： 10.3969/j.issn.1007-3969.2015.08.005.

摘要

背景与目的：微小RNA(microRNA，miRNA)是一类存在于真核生物体内只有19~39 bp大小的内源性非编码RNA，它能在转录和翻译水平调控基因的表达，在细胞的增殖分化、新陈代谢、免疫调控和凋亡等方面起着重要的作用。本研究检测miR-216a-5p在肺癌组织和肺癌细胞系的表达并探讨其对肺癌细胞侵袭能力的影响及其调控机制。方法：使用实时荧光定量PCR(quantitative real-time PCR，qRT-PCR)检测55例肺癌患者的肺癌组织和7种肺癌细胞系中miR-216a-5p的表达情况；miR-216a-5p瞬时转染A549、95D和H460 3种肺癌细胞系，使用Transwell侵袭实验检测miR-216a-5p对肺癌细胞系侵袭能力的影响；预测并构建miR-216a-5p的候选靶基因基质金属蛋白酶16(matrix metalloproteinase 16，MMP16)基因的双荧光素酶报告基因表达质粒，使用qRT-PCR和蛋白［质］印迹法(Western blot)检测miR-216a-5p对靶基因MMP16的mRNA和蛋白表达的影响；小干扰RNA(siRNA)干扰MMP16与上调miR-216a-5p对比检测其对肺癌细胞侵袭能力的影响。结果：90.91%(50/55)的肺癌患者肿瘤组织中miR-216a-5p表达明显低于对应的癌旁组织(P0.05)。7种肺癌细胞系中miR-216a-5p的表达量仅为对照组的7.00%~32.00%(P0.05)。上调miR-216a-5p的表达能够抑制肺癌细胞的侵袭；siRNA干扰MMP16与转染上调miR-216a-5p都能够抑制肺癌细胞中MMP16的表达，并抑制肺癌细胞侵袭。结论：miR-216a-5p可以作为临床肺癌诊断的候选标志物之一，并且其能够通过下调MMP16的表达从而抑制肺癌细胞的侵袭。

Abstract

Background and purpose: MicroRNA (miRNA) belongs to a class of 19 to 30 nucleotidelong

endogenous noncoding RNA expressed in eukaryotes and predominantly inhibits gene expression at the posttranscriptional level. The miRNAs play critical roles in cell proliferation and differentiation

apoptosis

metabolism

and immune regulation. This study aimed to detect the expression of miR-216a-5p in lung cancer tissues and lung cancer cell lines

and to discuss the effects of miR-216a-5p on the invasion ability of lung cancer cells and the mechanism. Methods: Quantitative real-time PCR (qRT-PCR) was used to detect the expression of miR-216a-5p in lung cancer tissues of 55 cases and 7 lung cancer cell lines. Three lung cancer cell lines of A549

95D and H460 were transiently transfected by miR-216a-5p

and Transwell was used to detect the effects of miR-216a-5p on the invasion of lung cancer cell lines. The dual luciferase reporter plasmids containing the miR-216a-5p candidate target gene and the gene of matrix metalloproteinase 16 (MMP16) were predicted and constructed. qRT-PCR and Western blot were used to detect the changes in mRNA and protein levels of target gene MMP16 by miR-216a-5p. The interference of MMP16 by siRNA and up-regulation miR-216a-5p by transfection were compared on the invasion of lung cancer cells. Results: The miR-216a-5p expression levels were all significantly reduced in 90.91% (50 of 55 patients) tumor tissues compared with corresponding adjacent normal lung tissues (P0.05). The miR-216a-5p expression levels were only 7.00%-32.00% in 7 lung cancer cells compared with the control group (P0.05). Up-regulation of the expression of miR-216a-5p inhibited the invasion of lung cancer cells; interference of MMP16 by siRNA

as well as up-regulating miR-216a-5p by transfection

inhibited the expression of MMP16 in lung cancer leading to inhibition of the invasion of lung cancer cells. Conclusion: miR-216a-5p can be a candidate marker in clinical diagnosis and it can inhibit the invasion of lung cancer cells by down-regulating the expression of MMP16.

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