文章摘要
孙党泽,丁 超,朱昌生,张 潍,刘士源,马震川,李 宇.miR-199a-3p负调控CBX7影响肺癌细胞NCI-H460的生物学行为研究[J].,2020,(3):455-459
miR-199a-3p负调控CBX7影响肺癌细胞NCI-H460的生物学行为研究
Investigate the Effect of miR-199a-3p on the Biological Behavior of NCI-H460 Lung Cancer Cells by Negatively Regulating CBX7
投稿时间:2019-06-24  修订日期:2019-07-18
DOI:10.13241/j.cnki.pmb.2020.03.011
中文关键词: 肺癌  微小RNA  miR-199a-3p  CBX7
英文关键词: Lung cancer  miRNA  miR-199a-3p  CBX7
基金项目:国家自然科学基金青年科学基金项目(81602023)
作者单位E-mail
孙党泽 西安市胸科医院胸外科 陕西 西安 710100 sundangze_xb@yeah.net 
丁 超 西安市胸科医院胸外科 陕西 西安 710100  
朱昌生 西安市胸科医院胸外科 陕西 西安 710100  
张 潍 西安交通大学第二附属医院胸外科 陕西 西安 710004  
刘士源 西安交通大学第二附属医院胸外科 陕西 西安 710004  
马震川 西安交通大学第二附属医院胸外科 陕西 西安 710004  
李 宇 西安交通大学第二附属医院胸外科 陕西 西安 710004  
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中文摘要:
      摘要 目的:探讨miR-199a-3p负调控CBX7影响肺癌细胞NCI-H460的生物学行为。方法:qRT-PCR法检测并比较肺癌组织、癌旁正常组织、肺癌细胞、正常肺上皮细胞中的miR-199a-3p mRNA相对表达量。比较远处转移肺癌组织、未转移肺癌组织中miR-199a-3p mRNA相对表达量。qRT-PCR法、Western Blot法检测并比较肺癌组织、癌旁正常组织中的CBX7 mRNA及蛋白的表达水平。荧光素酶活性法检测miR-199a-3p 与靶基因CBX7 的结合。比较miR-199a-3p模拟物转染组与阴性对照组的肺癌细胞中的CBX7 mRNA相对表达量及CBX7蛋白表达水平。CCK8实验检测miR-199a-3p对肺癌细胞增殖的促进作用。Tranwell实验检测miR-199a-3p对肺癌细胞侵袭与迁移能力的影响。结果:肺癌组织中miR-199a-3p 明显高于癌旁正常组织,发生远处转移的肺癌组织中miR-199a-3p mRNA的表达量明显高于未发生转移的肺癌组织,差异有统计学意义(P<0.001)。肺癌组织中CBX7 mRNA、CBX7蛋白表达水平均明显低于癌旁正常组织,差异有统计学意义(P<0.001)。荧光素酶活性法证实miR-199a-3p 可与靶基因CBX7结合抑制CBX7的表达。肺癌细胞中miR-199a-3p mRNA的相对表达量明显高于正常肺上皮细胞,CBX7 mRNA相对表达量明显低于正常肺上皮细胞(P<0.05)。对于肺癌细胞,miR-199a-3p模拟物转染组的CBX7 mRNA相对表达量及CBX7蛋白表达水平均明显低于阴性对照组(P<0.001)。CCK8实验证实miR-199a-3p能够促进肺癌细胞的增殖,Tranwell实验证实miR-199a-3p对肺癌细胞侵袭与迁移具有积极的促进作用。结论:miR-199a-3p在肺癌的发生发展过程中发挥重要作用,能够通过抑制CBX7基因的表达,促进肺癌细胞的增殖、侵袭和转移。
英文摘要:
      ABSTRACT Objective: To explore the effect of miR-199a-3p on the biological behavior of NCI-H460 lung cancer cells by negatively regulating CBX7. Methods: The relative expressions of miR-199a-3p mRNA in lung cancer tissues, adjacent normal tissues, lung cancer cells and normal lung epithelial cells were detected and compared by qRT-PCR. The relative expression levels of miR-199a-3p mRNA in distant metastatic lung cancer tissues and non-metastatic lung cancer tissues were compared. The expression levels of CBX7 mRNA and protein in lung cancer tissues and adjacent normal tissues were detected by qRT-PCR and Western Blot. The binding of miR-199a-3p to target gene CBX7 was detected by luciferase activity. CBX7 mRNA expression levels and CBX7 protein expression levels in lung cancer cells transfected with miR-199a-3p mimics and the negative control group were compared. CCK8 assay detected the promoting effect of miR-199a-3p on the proliferation of lung cancer cells. Tranwell assay examined the effect of miR-199a-3p on invasion and migration of lung cancer cells. Results: miR-199a-3p in lung cancer tissues was significantly higher than that in adjacent normal tissues, and the expression level of miR-199a-3p mRNA in lung cancer tissues with distant metastasis was significantly higher than that in lung cancer tissues without metastasis, the difference was statistically significant(P<0.001). The expression levels of CBX7 mRNA and CBX7 protein in lung cancer tissues were significantly lower than those in adjacent normal tissues(P<0.001). Luciferase activity confirmed that miR-199a-3p could bind to target gene CBX7 and inhibit the expression of CBX7.The relative expression level of miR-199a-3p mRNA in lung cancer cells was significantly higher than that in normal lung epithelial cells, and the relative expression level of CBX7 mRNA was significantly lower than that in normal lung epithelial cells (P<0.05). For lung cancer cells, the relative mRNA expression level and CBX7 protein expression level of miR-199a-3p mimics transfected group were significantly lower than those of the negative control group(P<0.001). CCK8 assay confirmed that miR-199a-3p could promote the proliferation of lung cancer cells, and Tranwell assay confirmed that miR-199a-3p had a positive promoting effect on the invasion and migration of lung cancer cells. Conclusion: miR-199a-3p plays an important role in the occurrence and development of lung cancer, and can promote the proliferation, invasion and metastasis of lung cancer cells by inhibiting the expression of CBX7 gene.
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