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

doi:10.3969/j.issn.1005-4979.2014.03.004

Abstract

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

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

CLC Number:

R739.8
Q754

MO Xian-chao, LI Wei-zhong. siRNA-mediated COX-2 Gene Silencing Inhibits the Proliferation and Invasion of KB/VCR Cell Lines[J]. 《Journal of Oral and Maxillofacial Surgery》, 2014, 24(3): 180-.

莫显超，李伟忠. siRNA沉默COX-2基因对KB/VCR细胞的增殖及侵袭的影响[J]. 《口腔颌面外科杂志》, 2014, 24(3): 180-.

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URL: https://journal06.magtech.org.cn/Jweb_joms/EN/10.3969/j.issn.1005-4979.2014.03.004

https://journal06.magtech.org.cn/Jweb_joms/EN/Y2014/V24/I3/180

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