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作 者:尹逊海[1] 姜爱民[1] 张秀峰[1] 梁桃[1]
机构地区:[1]哈尔滨医科大学附属第一临床医学院消化内科,黑龙江哈尔滨150001
出 处:《中国临床医学》2007年第1期29-30,共2页Chinese Journal of Clinical Medicine
摘 要:目的:探讨选择性环氧化酶2(COX-2)抑制剂对COX-2高表达的结肠癌细胞株HT-29增殖和凋亡的影响,明确以COX-2为靶点治疗结肠癌的作用途径。方法:将选择性COX-2抑制剂尼美舒利(nimesulide)按不同浓度作用于结肠癌细胞系HT-29,用MTT(四甲基偶氮唑蓝比色法)法分别于0、24、48、72h检测细胞增殖状态;流式细胞仪观察尼美舒利对细胞凋亡的影响,进一步采用ELISA法检测药物作用后前列腺素E2(PGE2)的表达,免疫组化法测定内皮细胞生长因子(VEGF)表达阳性率。结果:尼美舒利对结肠癌细胞系HT-29呈时间、剂量依赖性方式抑制细胞增殖,促进其凋亡。PEG2及VEGF表达水平随作用时间延长而下降。结论:选择性COX-2抑制剂可能通过PGE2与VEGF途径影响结肠癌细胞HT-29的增殖与凋亡,是其治疗结肠癌的分子机制。Objective:To investigate the influence of nimesulide, a selective cyclooxygenase-2(COX-2) inhibitor, on the prolfieration and apoptosis of colorectal cancer cell HT-29, and to explore it's potential mechanism to treat colorectal carcinoma, Methods:Cultured HT-29 cells were treated with nimesulide. MTT assay and flow cytometry were used to measure the prolifer- ation and apoptosis in 0,24,48,72 h respectively. The expression of PGE2 and VEGF was detected by ELISA and immunohistochemistry methods separately after treatment With nimesulide. Results: Nimesulide inhibited the cells proliferation and induced apoptosis in a dose- and time-dependent manner, and resulted in a significant down-regulation of PGE2 and VEGF. Conclusion:Our results showed that Nimesulide may inhibit the proliferation and induce apoptosis of colon cancer cell through decreasing expression of PGE2 and VEGF. This may be a new interfering target of selective COX-2 inhibitor on treating colon cancer.
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