吉林大学学报(医学版) ›› 2020, Vol. 46 ›› Issue (02): 233-239.doi: 10.13481/j.1671-587x.20200205

• 基础研究 • 上一篇    下一篇

奥沙利铂对人舌鳞癌CAL27细胞增殖和凋亡的影响及其机制

张楚1, 郝苗2, 王会俞1, 王晓峰1, 张天夫1   

  1. 1. 吉林大学中日联谊医院口腔科, 吉林 长春 130033;
    2. 吉林大学中日联谊医院科研中心, 吉林 长春 130033
  • 收稿日期:2019-10-20 发布日期:2020-04-07
  • 通讯作者: 张天夫,教授,主任医师,硕士研究生导师(Tel:0431-84995573,E-mail:zhangtianfu1963@sina.com);王晓峰,副教授,副主任医师,硕士研究生导师(Tel:0431-84995573,E-mail:xiaofeng2238@sina.com) E-mail:zhangtianfu1963@sina.com;xiaofeng2238@sina.com
  • 作者简介:张楚(1993-),女,河南省郑州市人,在读医学硕士,主要从事口腔肿瘤发病机制方面的研究。
  • 基金资助:
    国家自然科学基金资助课题(81903881);吉林省发改委科研基金资助课题(2018C007);吉林省卫健委科研基金资助课题(2017F007,2019SCZ006);吉林大学白求恩计划科研基金资助课题(2018B02)

Effect of Oxaliplatin on proliferation and apoptosis of human tongue squamous cell carcinoma CAL27 cells and its mechanism

ZHANG Chu1, HAO Miao2, WANG Huiyu1, WANG Xiaofeng1, ZHANG Tianfu1   

  1. 1. Department of Stomatology, China-Japan Union Hospital, Jilin University, Changchun 130033, China;
    2. Scientific Research Center, China-Japan Union Hospital, Jilin University, Changchun 130033, China
  • Received:2019-10-20 Published:2020-04-07

摘要: 目的:探讨奥沙利铂(Oxaliplatin)对人舌鳞状细胞癌(简称舌鳞癌)CAL27细胞增殖和凋亡的影响,并阐明其潜在作用机制。方法:采用不同浓度(0、10、20、40和80 mg·L-1)Oxaliplatin处理CAL27细胞,分别作为对照组和10、20、40及80 mg·L-1 Oxaliplatin组,采用结晶紫染色法观察各组CAL27细胞形态表现,CCK-8法检测各组CAL27细胞增殖率,流式细胞术检测不同细胞周期CAL27细胞百分比和凋亡率,实时荧光定量PCR法检测各组CAL27细胞中周期蛋白依赖性激酶2(CDK2)和细胞周期蛋白E(cyclin E)mRNA表达水平,Western blotting法检测各组CAL27细胞中抗凋亡蛋白survivin和促凋亡蛋白Bax的表达水平。结果:与对照组比较,40 mg·L-1 Oxaliplatin组CAL27细胞出现一定程度的皱缩,80 mg·L-1 Oxaliplatin组CAL27细胞明显失去原有形态,细胞间连接丧失。与对照组比较,10、20、40和80 mg·L-1 Oxaliplatin组CAL27细胞增殖率明显降低(P<0.05或P<0.01)。与对照组比较,40 mg·L-1 Oxaliplatin组G0/G1期CAL27细胞百分比明显升高(P<0.01),CDK2和cyclin E mRNA表达水平明显降低(P<0.05)。与对照组比较,40与80 mg·L-1 Oxaliplatin组CAL27细胞凋亡率明显升高(P<0.01)。与对照组比较,40和80 mg·L-1 Oxaliplatin组CAL27细胞中survivin蛋白表达水平明显降低(P<0.01),Bax蛋白表达水平则明显升高(P<0.05或P<0.01)。结论:Oxaliplatin能够抑制CAL27细胞增殖,促进细胞凋亡,其机制可能与细胞发生G0/G1期阻滞以及survivin蛋白表达水平降低和Bax蛋白表达水平升高有关。

关键词: 舌鳞状细胞癌, 奥沙利铂, 细胞增殖, 细胞凋亡, 细胞周期

Abstract: Objective: To explore the effect of Oxaliplatin on the proliferation and apoptosis of human tongue squamous cell carcinoma CAL27 cells, and to clarify its underlying mechanism. Methods: The CAL27 cells were treated with different concentrations of Oxaliplatin (0,10, 20, 40 and 80 mg·L-1) and used as control group and 10, 20, 40 and 80 mg·L-1 Oxaliplatin groups. The morphology of CAL27 cells in various groups were observed by crystal violet staining. The proliferation rates of the CAL27 cells in various groups were detected by CCK-8 assay. The percentages of CAL27 cells in different cell cycles and the apoptotic rates in various groups were detected by flow cytometry. The expression levels of cyclin-dependent kinase 2(CDK2)and E-type cyclin(cyclin E) mRNA in the CAL27 cells in various groups were analyzed by Real-time fluorescence quantitative PCR. The expression levels of anti-apoptotic protein survivin and pro-apoptotic protein Bax in the CAL27 cells in various groups were determined by Western blotting method. Results: Compared with control group, the CAL27 cells in 40 mg·L-1 Oxaliplatin group wrinkled; the cells in 80 mg·L-1 Oxaliplatin group lost the former morphology, and the intercellular connections of cells disapeared. Compared with control group, the proliferation rates of CAL27 cells in 10, 20, 40 and 80 mg·L-1 Oxaliplatin groups were significantiy decreased (P<0.05 or P<0.01).Compared with control group, the percentage of CAL27 cells in G0/G1 phase in 40 mg·L-1 Oxaliplatin group was significantly increased (P<0.01), and the expression levels of CDK2 and cyclin E mRNA were significantly decreased (P<0.05).Compared with control group, the apoptptic rates of CAL27 cells in 40 and 80 mg·L-1 Oxaliplatin groups were markedly increased (P<0.01). Compared with control group, the expression levels of survivin protein in CAL27 cells in 40 and 80 mg·L-1 Oxaliplatin groups were significantly decreased (P<0.01), and the expression levels of Bax protein were obviously increased (P<0.05 or P<0.01). Conclusion: Oxaliplatin can inhibit the proliferation and induce the apoptosis of CAL27 cells, and its mechanism may be related to arresting G0/G1 phase, up-regulating the expression level of survivin and down-regulating the expression level of Bax.

Key words: tongue squamous cell carcinoma, Oxaliplatin, cell proliferation, apoptosis, cell cycle

中图分类号: 

  • R739.86