《口腔颌面外科杂志》 ›› 2014, Vol. 24 ›› Issue (3): 180-. doi: 10.3969/j.issn.1005-4979.2014.03.004

• 基础研究 • 上一篇    下一篇

siRNA沉默COX-2基因对KB/VCR细胞的增殖及侵袭的影响

莫显超,李伟忠   

  1. 南方医科大学南方医院口腔颌面外科,广东   广州   510515
  • 出版日期:2014-05-28 发布日期:2015-06-24
  • 通讯作者: 李伟忠,教授. E-mail:gzliwz@126.com
  • 作者简介:莫显超(1988—),男,广州人,硕士研究生.
  • 基金资助:

    广东省自然科学基金项目(S2011010003841,S2013010014551);广东省科技计划项目(2012B031800468)

siRNA-mediated COX-2 Gene Silencing Inhibits the Proliferation and Invasion of KB/VCR Cell Lines

MO Xian-chao, LI Wei-zhong   

  1. Department of Oral and Maxillofacial Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, Guangdong  Province, China
  • Online:2014-05-28 Published:2015-06-24

摘要: 目的:观察siRNA沉默口腔癌耐长春新碱细胞株KB/VCR细胞COX-2基因后,对KB/VCR细胞增殖及侵袭能力的影响。方法:将KB/VCR细胞分为COX-2 siRNA组、阴性对照组及空白对照组,采用RT-PCR检测各组细胞COX-2 mRNA的表达,蛋白印迹法检测COX-2蛋白的表达,MTT法检测各组细胞的生长抑制率,Transwell小室测定各组细胞侵袭能力的变化。结果:COX-2 siRNA组细胞的COX-2蛋白和mRNA的表达明显低于阴性对照组和空白对照组(P<0.01)。COX-2 siRNA组细胞的生长抑制率明显高于阴性对照组和空白对照组(P<0.01)。COX-2 siRNA组细胞的侵袭能力也明显降低。结论:COX-2 siRNA能特异性沉默KB/VCR细胞的COX-2基因,使KB/VCR细胞生长得到抑制,并减弱其侵袭能力。

关键词: KB/VCR细胞, 环氧化酶-2, 小干扰RNA, 增殖, 侵袭

Abstract: Objective: To investigate the effect of small interfering RNA-mediated (siRNA-mediated) COX-2 gene silencing to change the proliferation and invasion behavior of KB/VCR cell lines. Methods: The KB/VCR cells were divided into 3 groups ,which were COX-2 siRNA group, negative control group, blank control group. The transcription of COX-2 gene was examined with RT-PCR. The protein expression of COX-2 was determined by Western blotting. MTT assay was used to analyze the proliferation of KB/VCR cells. The cell invasion was evaluated using a transwell assay. Results: COX-2 mRNA and protein levels were significantly reduced in COX-2 siRNA group (P<0.01). The growth inhibition of KB/VCR cells in COX-2 siRNA group was significantly higher than other groups (P<0.01). Meanwhile, the invasiveness of KB/VCR cells in COX-2 siRNA group was decreased remarkably. Conclusion: siRNA-mediated COX-2 gene silencing can increase the growth inhibition in KB/VCR cells and down regulate the cell invasion.

Key words: KB/VCR cell, cyclooxygenase-2, siRNA, proliferation, ivasion

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