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中国应用生理学杂志 ›› 2022, Vol. 38 ›› Issue (1): 53-57.doi: 10.12047/j.cjap.6206.2022.010

• 研究论文 • 上一篇    下一篇

长链非编码RNA Linc00673过表达对胃癌MGC-803细胞增殖与凋亡的影响*

郭红艳1, 徐亚茹2, 李耕慧3, 孙晓杰4△, 赵正林1, 吴琦4, 刘波5   

  1. 1.齐齐哈尔医学院生化教研室, 2.齐齐哈尔医学院附属第一医院检验科, 3.齐齐哈尔市第一医院老年科, 4.齐齐哈尔医学院临床生化教研室, 5.齐齐哈尔医学院附属第二医院办公室, 齐齐哈尔 161006
  • 收稿日期:2021-05-13 修回日期:2021-12-24 出版日期:2022-01-28 发布日期:2022-05-30
  • 通讯作者: Tel: 0452-2663151; E-mail: sunxj97@163.com
  • 基金资助:
    * 黑龙江省省属本科高校基本科研业务费项目(2019-KYYWF-1219)

Effects of long-chain noncoding RNA Linc00673 overexpression on proliferation and apoptosis of gastric cancer cell line MGC-803

GUO Hong-yan1, XU Ya-ru 2, LI Geng-hui3, SUN Xiao-jie4△, ZHAO Zheng-lin1, WU Qi4, LIU Bo5   

  1. 1. Department of Biochemistry, Qiqihar Medical College, 2. The Clinical laboratory, the First Affiliated Hospital of Qiqihar Medical College, 3. Cadre Ward, the First Hospital of Qiqihar, 4. Department of Clinical Biochemistry, Qiqihar Medical College, 5. Office of the Second Affiliated Hospital of Qiqihar Medical College, Qiqihar 161006, China
  • Received:2021-05-13 Revised:2021-12-24 Online:2022-01-28 Published:2022-05-30

摘要: 目的: 探讨长链非编码RNA Linc00673过表达对胃癌细胞增殖和凋亡的影响及其机制。方法: 将重组慢病毒表达质粒pLVX-Linc00673和对照空载体质粒pLVX-NC在293T细胞中进行慢病毒包装与扩增,将重组慢病毒转染胃癌细胞MGC-803建立稳定过表达 Linc00673的细胞系,实时荧光定量PCR方法检测Linc00673基因的表达; MTT实验和克隆形成实验观察细胞的生长增殖;流式细胞术检测细胞周期和细胞凋亡;qPCR检测细胞周期相关调控基因表达;免疫印迹法检测PI3K/Akt信号通路关键分子及肿瘤增殖相关蛋白的表达。结果: Linc00673在胃癌细胞系MGC-803、BGC-823和AGS中的表达量显著高于正常胃粘膜细胞GES-1(P<0.05)。建立了稳定过表达Linc00673的MGC-803细胞系,Linc00673的表达量比对照空载体组高200倍。Linc00673过表达促进MGC-803细胞增殖和克隆形成(P<0.05),抑制细胞凋亡并影响细胞周期G1→S期进程(P<0.01);Linc00673过表达可影响MGC-803细胞周期调节基因CCNG2、p19和CDK1的表达;免疫印迹结果显示,Linc00673过表达不仅促进PI3K/Akt信号通路关键分子pAKT及其下游靶点NF-κB和Bcl-2蛋白的表达,而且上调肿瘤相关因子β-catenin和EZH2蛋白的表达。结论: Linc00673过表达可能通过PI3K/Akt信号通路促进MGC-803细胞增殖、抑制凋亡。

关键词: Linc00673, 胃癌, 细胞增殖, 细胞凋亡, PI3K/Akt信号通路

Abstract: Objective: To investigate the effects of long-chain noncoding RNA Linc00673 overexpression on proliferation and apoptosis of gastric cancer cells and its mechanisms. Methods: The recombinant lentivirus expressing plasmid pLVX-Linc00673 and the control empty plasmid pLVX-NC were packaged and amplified in 293T cells, and the recombinant lentivirus was transfected into gastric cancer cell line MGC-803 to establish a cell line stably overexpressing Linc00673. The expression of Linc00673 gene was detected by real-time fluorescence quantitative PCR. The growth and proliferation of cells were observed by MTT assay and clone formation assay. Cell cycle and apoptosis were detected by flow cytometry. The expressions of cell cycle related regulatory genes were detected by qPCR. The expressions of key molecules in the PI3K/Akt signaling pathway and tumor proliferation related proteins were detected by Western blot. Results: The expressions of Linc00673 in gastric cancer cell line MGC-803, BGC-823 and AGS were significantly higher than that in normal gastric mucosa cell line GES-1 (P<0.05). MGC-803 cell line with stable overexpression of LINC00673 was established, and the expression level of LincC00673 was 200 times higher than that of the control empty carrier group. Overexpression of Linc00673 promoted proliferation of MGC-803 cells (P<0.05) and clone formation (P<0.05), inhibited cell apoptosis and affected the G1→S phase progression of cell cycle (P<0.01). Overexpression of Linc00673 could affect the expressions of cell cycle regulatory gene CCNG2, P19 and CDK1 in MGC-803. Western blot showed that Linc00673 overexpression not only promoted the expressions of the key molecule pAkt in PI3K / Akt signaling pathway and its downstream target NF-κ B and Bcl-2 protein, but also up regulated the expressions of tumor related factors β-catenin and EZH2 proteins. Conclusion: Overexpression of Linc00673 may promote proliferation and inhibit apoptosis of MGC-803 cells through PI3K/Akt signaling pathway.

Key words: Linc00673, gastric cancer, cell proliferation, apoptosis, PI3K/Akt signal pathway

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