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lncRNASNHG11通过吸附miR-193a-5p促进NSCLC细胞A549的恶性生物学行为
引用本文:王羽,曹佳丽,陈哲聪,高梦源,陈文虎.lncRNASNHG11通过吸附miR-193a-5p促进NSCLC细胞A549的恶性生物学行为[J].中国肿瘤生物治疗杂志,2022,29(2):108-113.
作者姓名:王羽  曹佳丽  陈哲聪  高梦源  陈文虎
作者单位:杭州医学院药学院;杭州医学院临床医学院;杭州医学院基础医学与法医学院 生物化学与分子生物学教研室
基金项目:浙江省中医药科技计划项目(No. 2021ZB078);浙江省大学生创新创业项目(No. 202113023001;No. 202113023009)
摘    要:目的: 探讨lncRNA SNHG11对非小细胞肺癌(NSCLC)A549细胞增殖、侵袭和迁移的影响及其可能机制。 方法:qPCR检测人胚肺细胞HEL-1和NSCLC细胞A549、H1299、HCC827中lncRNASNHG11和miR-193a-5p的表达水平,向A549细胞中转染SNHG11小干扰RNA(si-SNHG11)、miR-193a模拟物(miR-193a mimic)或miR-193a抑制剂(miR-193a inhibitor)后,CCK-8法检测其对细胞增殖的影响,Transwell小室和细胞划痕实验检测对细胞侵袭和迁移的影响,WB法检测对细胞增殖抗原Ki67、细胞周期蛋白D1 (cyclin D1)表达的影响,双荧光素酶报告实验验证lncRNASNHG11与miR-193a-5p的靶向关系。 结果: 与人胚肺细胞HEL-1相比,NSCLC细胞A549、H1299、HCC827中lncRNA SNHG11均呈高表达、miR-193a-5p呈低表达(均P<0.05);沉默lncRNA SNHG11可抑制A549细胞的增殖、侵袭和迁移,降低细胞中Ki67和Cyclin D1蛋白的表达水平(均P<0.05);过表达miR-193a-5p可抑制A549细胞增殖和侵袭迁移(均P<0.05)。lncRNASNHG11可靶向吸附miR-193a-5p,抑制miR-139a-5p可部分逆转沉默lncRNA SNHG11对A549细胞增殖、侵袭和迁移的作用(均P<0.05)。 结论:lncRNA SNHG11通过吸附miR-193a-5p促进NSCLCA549细胞的增殖、侵袭和迁移。

关 键 词:非小细胞肺癌  A549细胞  lncRNASNHG11  miR-193a-5p  增殖  侵袭  迁移

lncRNA SNHG11 promotes the malignant biological behaviors of NSCLC A549 cells by adsorbing miR-193a-5p
WANG Yu,CAO Jiali,CHEN Zhecong,GAO Mengyuan,CHEN Wenhu.lncRNA SNHG11 promotes the malignant biological behaviors of NSCLC A549 cells by adsorbing miR-193a-5p[J].Chinese Journal of Cancer Biotherapy,2022,29(2):108-113.
Authors:WANG Yu  CAO Jiali  CHEN Zhecong  GAO Mengyuan  CHEN Wenhu
Affiliation:School of Pharmacy, Hangzhou Medical College;School of Clinical Medicine, Hangzhou Medical College; Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences & Forensic Medicine, Hangzhou Medical College
Abstract:Objective: To investigate the effect of lncRNA SNHG11 on the proliferation, invasion and migration of non-small cell lung cancer (NSCLC) A549 cells and its possible mechanisms. Methods: qPCR was used to detect the levels of lncRNA SNHG11 and miR- 193a-5p in human embryonic lung cells (HEL-1) and lung cancer cells (A549, H1299, and HCC827). A549 cells were transfected with SNHG11 small interfering RNA (si-SNHG11), miR-193a mimic or miR-193a inhibitor. The proliferation of A549 cells was detected by CCK-8 assay, migration and invasion of A549 cells were detected by Wound healing and Transwell assay, the protein expression of Ki67 and Cyclin D1 was determined by Western blot, and the targeting relationship between lncRNA SNHG11 and miR-193a-5p was verified by Dual-luciferase reporter experiment. Results: Compared with HEL-1 cells, the expression level of lncRNA SNHG11 was significantly increased while the expression of miR-193a-5p was decreased in lung cancer A549, H1299 and HCC827 cells (all P<0.05). Silencing lncRNA SNHG11 inhibited the proliferation, migration and invasion of A549 cells and reduced the protein expression of Ki67 and Cyclin D1 (all P<0.05). Over-expression of miR-193a-5p inhibited the proliferation, migration and invasion of A549 cells (all P<0.05). lncRNA SNHG11 could targetedly adsorb miR-193a-5p. miR-139a-5p inhibition could partially reverse the effect of silencing lncRNA SNHG11 on the proliferation, invasion and migration of A549 cells (all P<0.05). Conclusion: lncRNA SNHG11 promotes the proliferation, invasion and migration of NSCLC cells by adsorbing miR-193a-5p.
Keywords:NSCLC  A549 cell  lncRNASNHG11  miR-193a-5p  proliferation  migration  invasion
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