《口腔颌面外科杂志》 ›› 2020, Vol. 30 ›› Issue (2): 74-79. doi: 10.3969/j.issn.1005-4979.2020.02.003

• 基础研究 • 上一篇    下一篇

沉默信息调节因子3对舌癌细胞凋亡的影响

袁玮(), 周骥驰, 李曼, 程龙, 杨金锁, 殷博雅, 黄欣()   

  1. 首都医科大学附属北京口腔医院口腔颌面头颈肿瘤外科,北京 100050
  • 收稿日期:2019-11-28 修回日期:2020-02-23 出版日期:2020-04-28 发布日期:2020-04-24
  • 通讯作者: 黄 欣,主任医师. E-mail:
  • 作者简介:

    袁 玮(1994—),女,山东青岛人,硕士研究生. E-mail:

  • 基金资助:
    北京市教育委员会科技计划及社科计划资助项目(KM201710025020)

SIRT3 Regulates Apoptosis of Tongue Squamous Cell Carcinoma Cells in Vitro

YUAN Wei(), ZHOU Jichi, LI Man, CHENG Long, YANG Jinsuo, YIN Boya, HUANG Xin()   

  1. Department of Oral and Maxillofacial Head and Neck Oncology, Beijing Stomatological Hospital, Capital Medical University, Beijing 100050,China
  • Received:2019-11-28 Revised:2020-02-23 Online:2020-04-28 Published:2020-04-24

摘要:

目的:探讨沉默信息调节因子3(sirtuin3,SIRT3)对舌癌细胞凋亡的影响。方法:采用小干扰RNA(small interfere RNA,siRNA)沉默舌癌细胞中的SIRT3。MTT法检测SIRT3沉默对舌癌细胞增殖活力的影响;TUNEL染色检测SIRT3沉默对舌癌细胞凋亡的影响;酶联免疫吸附实验(enzyme linked immunosorbent assay, ELISA)检测SIRT3沉默对舌癌细胞半胱氨酸天冬氨酸蛋白酶-3(Caspase-3)活性的影响;蛋白质免疫印迹法(Western blot)检测SIRT3沉默对舌癌细胞Caspase-3和多聚二磷酸腺苷核糖聚合酶(poly ADP-ribose polymerase, PARP)表达的影响。结果:SIRT3沉默有效,在SIRT3沉默后观察到舌癌细胞的增殖活力降低,细胞凋亡增加,Caspase-3活性增加,Caspase-3和PARP表达增加。沉默SIRT3前后,舌癌细胞的增殖活力、TUNEL阳性细胞比例、Caspase-3的活性值以及Caspase-3和PARP表达水平差异有统计学意义(P<0.05)。结论:SIRT3沉默可促进舌癌细胞凋亡。

关键词: 沉默信息调节因子3, 舌鳞状细胞癌, 细胞凋亡

Abstract:

Objective: To explore the role of sirtuin3(SIRT3) in regulating the apoptosis of tongue squamous cell carcinoma (TSCC) cells in vitro. Methods: The knockdown of SIRT3 of TSCC cell lines were accomplished through small interfering RNA (siRNA). The proliferation activity of the TSCC cells was examined by MTT assay; the apoptosis of the TSCC cell lines was tested using TUNEL staining; the Caspase-3 activity of the cells was analyzed by enzyme-linked immunosorbent assay (ELISA); and the expression of Caspase-3 and PARP of 2 squamous cell carcinoma (SCC) cells was determined with Western blotting. Results: SIRT3 knockdown in TSCC cells significantly lowered the proliferation activity, increased the number of TUNEL-positive cells, enhanced the Caspase-3 activity, and the expression of Caspase-3 and PARP were significantly high in the two SCC cell lines than the control group. The proliferation activity, the number of TUNEL-positive cell, the activity of Caspase-3, and the expression of Caspase-3 and PARP in TSCC cells were significantly different before and after modulation of SIRT3 expression (P<0.05). Conclusion: Knockdown of SIRT3 plays a positive role for apoptosis of SCC cells in vitro.

Key words: sirtuin3(SIRT3), tongue squamous cell carcinoma, apoptosis

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