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选择性环氧合酶-2抑制剂对人类舌鳞癌Tea-8113细胞血管生成素蛋白表达的影响
引用本文:武云霞,李晓征,赵玮,王晓彦,郝凤翔.选择性环氧合酶-2抑制剂对人类舌鳞癌Tea-8113细胞血管生成素蛋白表达的影响[J].肿瘤研究与临床,2008,20(9):584-587.
作者姓名:武云霞  李晓征  赵玮  王晓彦  郝凤翔
作者单位:山西医科大学第一医院口腔科,030001
摘    要:目的研究选择性环氧合酶-2(COX-2)抑制剂尼美舒利(NIM)对人类舌鳞癌Tea-8113细胞血管生成素-1、2(Ang-1、Ang-2)蛋白表达的影响。方法体外培养人类舌鳞癌Tea-8113细胞,加入不同浓度的NIM(0、25、50、100、200μmol/L)进行干预,分别作用24、48、72h后,放射免疫法检测细胞培养上清液中PGE2分泌水平的改变,免疫组织化学(SP)方法检测人类舌鳞癌Tea-8113细胞内Ang-1和An舻2蛋白表达的变化情况。结果NIM呈浓度和时间依赖性地抑制PGE2分泌和Ang-2蛋白的表达,Ang-1蛋白表达受NIM影响不明显。结论NIM可减少PGE2分泌和Ang-2蛋白的表达,此机制可能是通过COX-2依赖性肿瘤血管生成抑制途径起作用。

关 键 词:前列腺素内过氧化物合酶类  环加氧酶抑制药  血管生成素-1  血管生成素-2  舌肿瘤    鳞状细胞
收稿时间:2007-8-3

Influence of COX-2 inhibitor on expression of Ang-1 and Ang-2 protein in human tongue squamous cell line Tca-8113
WU Yun-xia,LI Xiao-zheng,ZHAO Wei,WA NG Xioo-yan,HAO Feng-xiang.Influence of COX-2 inhibitor on expression of Ang-1 and Ang-2 protein in human tongue squamous cell line Tca-8113[J].Cancer Research and Clinic,2008,20(9):584-587.
Authors:WU Yun-xia  LI Xiao-zheng  ZHAO Wei  WA NG Xioo-yan  HAO Feng-xiang
Institution:WU Yun-xia, LI Xiao-zheng, ZHAO Wei, WANG Xiao-yan, HAO Feng-xiang( Dental Division, the First Hospital, Shanxi Medical University, Taiyuan 030001, China)
Abstract:Objective To investigate the influence of Nimesulide(NIM),a selective Cyclooxygenase-2 (COX-2) inhibitor, on the expression of Angiopoietin-1 (Ang-1) and Angiopoietin-2 (Ang-2) protein in human tongue squamous cell carcinoma Tca-8113 cell lines. Methods Tca-8113 cell were cultured in vitro, and exposed to a range of concentrations of nimesulide (NIM) (0, 25, 50, 100, 200 μmol/L) for 24 h, 48 h, 72 h, and the PGE2 level in the cells cultured supernate was quantitated by the radioimmunoassay, and the expression of Ang-1 and Ang-2 protein in human tongue squamous cell line Tca-8113 were measured by the SABC immunocytochemistry staining simultaneously. Results The PGE2 level in the cultured supematant and expression of Ang-2 in Tca-8113 cells decreased by NIM in a concentration and time dependent manner, but not Ang-1. Conclusion NIM can decrease PGE2 level and Ang-2 expression, which may be involved in the inhibition of cancer angiogenesis of COX-2 dependence mechanisms.
Keywords:Prostaglandin-Endoperofide synthases  Cycloaxygenase inhibitors  Angiopoietin-1  Angiopoietin-2  Tongue neoplasms  Carcinoma  squamous cell
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