基础医学与临床 ›› 2017, Vol. 37 ›› Issue (8): 1133-1139.

• 研究论文 • 上一篇    下一篇

PER2对人口腔鳞癌SCC15细胞增殖、凋亡以及生物钟基因表达的影响

敖奕然1,赵钦1,杨凯1,郑刚2   

  1. 1. 重庆医科大学 附属第一医院
    2. 重庆市中医研究院
  • 收稿日期:2016-07-07 修回日期:2016-11-01 出版日期:2017-08-05 发布日期:2017-07-17
  • 通讯作者: 杨凯 E-mail:cqfyyk@aliyun.com

Effect of PER2 on proliferation, apoptosis and clock gene expression in human oral squamous cell carcinoma SCC15 cells

  • Received:2016-07-07 Revised:2016-11-01 Online:2017-08-05 Published:2017-07-17
  • Contact: Kai YANG E-mail:cqfyyk@aliyun.com

摘要: 目的 探讨人口腔鳞癌SCC15细胞中生物钟基因PER2的表达改变对细胞增殖、凋亡以及其它生物钟基因的影响。方法 用RNA干扰技术沉默人口腔鳞癌SCC15细胞中PER2基因;流式细胞术检测细胞增殖和凋亡水平;实时荧光定量PCR检测生物钟基因CLOCK、BMAL1、PER1、PER3、DEC1、DEC2、CRY1、CRY2、TIM、CKIε、RORα、NPAS2和REV-ERBα mRNA表达。结果 沉默PER2后,SCC15细胞的增殖水平显著增加,凋亡显著下降(P <0.05);SCC15细胞中生物钟基因PER3、BMAL1、DEC1、DEC2、CRY2、TIM、RORα和NPAS2 mRNA的表达水平显著降低,PER1和REV-ERBα mRNA的表达显著升高(P <0.05)。结论 在癌细胞中,生物钟基因PER2对生物钟基因网络中其它生物钟基因具有重要调控作用,PER2表达降低导致细胞增殖增加和细胞凋亡水平下降。

关键词: 癌, 口腔, 生物钟基因, PER2

Abstract: Objectives To discuss the effect of alter-expressed PER2 on proliferation, apoptosis and other clock genes expression in human oral squamous cell carcinoma SCC15 cells. Method Short hairpin RNA interference was used to knockdown PER2 effectively in SCC15 human oral squamous cell carcinoma cells. Flow cytometry analysis was used to testify the cell proliferation and apoptosis. Quantitative real-time PCR was used to testify the mRNA expressions of PER3, BMAL1, DEC1, DEC2, CRY2, TIM, RORα, NPAS2, PER1 and REV-ERBα. Results The proliferation was enhanced and apoptosis was decreased obviously after PER2 knockdown in SCC15 cells (P<0.05). The mRNA expressions of PER3, BMAL1, DEC1, DEC2, CRY2, TIM, RORα and NPAS2 were significantly down-regulated, and the mRNA expressions of PER1 and REV-ERBα were significantly up-regulated (P<0.05). Conclusions Clock gene PER2 plays an important role in regulating other clock genes of the clock gene network in cancer cells, PER2 knockdown can enhance proliferation and recede apoptosis of cancer cell.

Key words: cancer, oral ?cavity, clock gene, PER2

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