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机构地区:[1]第三军医大学西南医院肿瘤科,重庆400038 [2]第三军医大学西南医院病理科,重庆400038
出 处:《实用医院临床杂志》2008年第3期56-58,共3页Practical Journal of Clinical Medicine
摘 要:目的探讨一磷酸腺苷活化蛋白激酶(AMPK)对环氧合酶-2(COX-2)蛋白表达及结肠癌5-氟尿嘧啶(5-Fu)化疗敏感性的影响。方法选用HT-29结肠癌细胞株,按照HT-29细胞的培养液不同,分为空白对照组(常规培养)、5-Fu培养组、5-氨基咪唑-4-甲酰胺核苷酸(AICAR)培养组、5-Fu+AICAR培养组。用western blot法测定各组中P-ACC和COX-2的表达,并分别于培养6、12、24小时分析5-Fu培养组和5-Fu+AICAR培养组中P-ACC和COX-2的表达水平的变化;用MTT法检测12、24、48小时各组细胞的存活率。结果5-Fu组作用后COX-2蛋白上调,AICAR致P-ACC表达后,可下调COX-2蛋白的表达;5-Fu联合AICAR可降低细胞存活率。结论AMPK的激活可能下调COX-2表达,并可能提高以5-Fu治疗为基础的结肠癌化疗敏感性。Objective To investigate the expression of cyclooxygenase-2 (COX-2) by the activation of adenosine monophosphate protein kinase (AMPK) and the relationship between the expression and chemosensitivity of 5-Fluorouracil in colon cancer. Methods We chose HT-29 colon carcinoma cells as our study object and divided them into 4 groups according to the culture media : blank control ( conventional culture) , 5-Fu, AICAR, 5-Fu + AICAR groups. Western blot were performed to detect the expression of P-ACC and COX-2 in each group, and the expression of P-ACC and COX-2 at 6, 12, 24 hours after culture in 5-Fu and 5-Fu + AICAR groups. Cell viability was measured by MTT. Results Compared with control group, we found upregulation of COX-2 in 5-Fu group and down-regulation of COX-2 when P-ACC had been expressed induced by AICAR in 5-Fu + AICAR group;Combination of 5-Fu and AICAR minimized cell viability. Conclusion Activation of AMPK can decrease the expression of COX-2, and may increase the chemosensitivity of 5-Fu drug in the treatment of colon cancer.
关 键 词:一磷酸腺苷活化蛋白激酶 环氧合酶-2 5-氟尿嘧啶 结肠癌 化疗敏感性
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