| miR-142-5p靶向转录因子YY1调控非小细胞肺癌上皮间质转化 |
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| 引用本文： | 张 峤1,张 健2,单 莉1. miR-142-5p靶向转录因子YY1调控非小细胞肺癌上皮间质转化[J]. 现代肿瘤医学, 2021, 0(23): 4080-4086. DOI: 10.3969/j.issn.1672-4992.2021.23.002 |
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| 作者姓名： | 张 峤1 张 健2 单 莉1 |
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| 作者单位： | 1.新疆医科大学附属肿瘤医院胸部肿瘤科，新疆 乌鲁木齐 830011;2.中国人民解放军69260部队卫生队，新疆 乌鲁木齐 830002 |
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| 基金项目： | 新疆维吾尔自治区卫生健康青年医学科技人才专项（编号:WJWY-201907） |
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| 摘 要： | 目的:探究miR-142-5p靶向转录因子YY1调控上皮间质转化（epithelial-mesenchymal transition,EMT）抑制非小细胞肺癌（non-small cell lung cancer,NSCLC）细胞体外转移的机制。方法:qRT-PCR检测肺癌细胞系中YY1和miR-142-5p表达水平;利用生物信息学软件预测并通过双荧光素酶报告基因实验验证miR-142-5p与YY1的结合位点；Transwell实验和划痕愈合实验分析YY1和miR-142-5p过表达对肺癌细胞迁移、侵袭的影响；Western blot与qRT-PCR检测各组细胞内EMT相关蛋白的表达变化。结果:YY1在不同肺癌细胞系中均表达上调，miR-142-5p表现为表达下调；双荧光素酶报告基因实验结果进一步验证了YY1与miR-142-5p的靶向结合相关性；抑制miR-142-5p表达水平能显著提高细胞中YY1表达，而miR-142-5p过表达能显著抑制肺癌细胞中YY1的表达水平，两者表达水平呈负相关；Transwell和划痕实验表明，YY1过表达能够促进肺癌细胞转移，而miR-142-5p过表达会抑制肺癌细胞转移；YY1过表达促进EMT相关蛋白的表达，而miR-142-5p作用相反。结论:miR-142-5p负向调控YY1作用于EMT相关分子表达，进而在体外抑制NSCLC细胞的转移。
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| 关 键 词： | miR-142-5p YY1 上皮间质转化 肺癌 |
miR-142-5p targeting YY1 regulating epithelial-mesenchymal transition in non-small cell lung cancer |
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| ZHANG Qiao1,ZHANG Jian2,SHAN Li1. miR-142-5p targeting YY1 regulating epithelial-mesenchymal transition in non-small cell lung cancer[J]. Journal of Modern Oncology, 2021, 0(23): 4080-4086. DOI: 10.3969/j.issn.1672-4992.2021.23.002 |
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| Authors: | ZHANG Qiao1 ZHANG Jian2 SHAN Li1 |
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| Affiliation: | 1.Department of Thoracic Oncology,Tumor Hospital Affiliated to Xinjiang Medical University,Xinjiang Urumqi 830011,China;2.Outpatient Department，People's Liberation Army 69260 Troops of Medical Team,Xinjiang Urumqi 830002,China. |
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| Abstract: | Objective:To explore the mechanism by which miR-142-5p targets YY1 to regulate epithelial-mesenchymal transition and inhibit the metastasis of non-small cell lung cancer cells in vitro and in vivo.Methods:qRT-PCR was used to detect the expression levels of YY1 and miR-142-5p in lung cancer cell lines.The dual-luciferase reporter gene assay was used to verify the targeted binding of miR-142-5p to YY1.The effect of YY1 and miR-142-5p on the cell migration and invasion by Transwell and wound-healing assay.Finally,the EMT-related proteins in each group were detected by Western blot and qRT-PCR.Results:The expression of YY1 was up-regulated and the miR-142-5p was down-regulated in lung cancer cell lines.The results of the dual-luciferase reporter assay further validated the targeted binding correlation between YY1 and miR-142-5p.Inhibiting the expression of miR-142-5p can increase the expression of YY1 significantly，However，overexpression of miR-142-5p inhibit the expression of YY1 in lung cancer cells.The expressions of YY1 and miR-142-5p in different lung cancer cell lines were negatively correlated.Transwell and wound-healing assay indicated that YY1 could enhance the metastasis ability of lung cancer cells，but overexpression of miR-142-5p could inhibit the metastasis ability of lung cancer cells.Overexpression of YY1 promotes the expression of EMT-related proteins.On the contrary，miR-142-5p constrained the expression of EMT related proteins.Conclusion:miR-142-5p may regulated the expression of EMT-related proteins by targeting YY1 involved in the lung cancer metastasis. |
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| Keywords: | miR-142-5p YY1 epithelial-mesenchymal transition lung cancer |
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