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环氧合酶-2抑制剂对人舌鳞癌Tca8113/BLM 细胞MDR1/P-gp表达的影响

Effect of Cyclooxygenase-2 Inhibitor on Expression of MDR1 mRNA and P-glycoprotein in Human Tongue Cancer Drug-resistance Cell Line Tca8113/BLM

  • 摘要: 目的 探讨环氧合酶-2抑制剂塞来昔布对人舌鳞癌耐药细胞系Tca8113/BLM细胞多药耐药基因和P-糖蛋白表达的影响。方法 采用BLM(30 μg/ml)反复24h暴露法处理人舌鳞癌细胞系Tca8113细胞,采用不同浓度的塞来昔布作用于Tca8113/BLM细胞,MTT法检测细胞增殖活性,流式细胞仪测定P-gp的表达水平,RT-PCR检测多药耐药基因mRNA的表达。结果 塞来昔布显著抑制Tca8113/BLM细胞增殖、下调Tca8113/BLM细胞MDR1基因表达,其作用呈剂量依赖关系。结论 塞来昔布以剂量依赖方式抑制人舌鳞癌耐药细胞系Tca8113/BLM细胞MD1l/P-gp表达,并抑制细胞增殖,这种作用可能与COX-2抑制剂增强抗癌药物对肿瘤细胞的杀伤作用有关。

     

    Abstract: Abstract:Objective To investigate the effect of celecoxib, a selective COX-2 inhibitor, on the expression of multidrug resistance gene (MDR1) and P-glycoprotein (P-gp) in human tongue cancer drug-resistance cell line Tca8113/BLM. Methods Human tongue squamous cell carcinoma cell line Tca8113 cells were repeatedly treated with BLM (30μg/ml) to establish drug-resistant cell line Tca8113/BLM. The inhibitory effect of celecoxib on Tca8113/BLM cell line was determined by MTT assay. The expression of P-gp and MRP were detected by flow cytometry and RT-PCR, respectively. Results The MTT results suggested that celecoxib inhibited the growth and proliferation of Tca8113/BLM cell lines in dose-dependent manner. Celecoxib treatment also resulted in significant down-regulated expression of MDR1 mRNA and P-gp. Conclusion Celecoxib shows a significant effect on inhibiting expression of MDR1 mRNA and P-gp in Tca8113/BLM cells, this is probably related to enhancing the lethal effects of anticancer agents against carcinoma cells.

     

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