化疗联合自噬抑制剂对结肠癌细胞钙调蛋白表达的影响

Q4 Biochemistry, Genetics and Molecular Biology 解放军医学杂志 Pub Date : 2016-04-01 DOI:10.11855/J.ISSN.0577-7402.2016.04.03
R. Peng, D. Li, Ya Ding, Xingjie Zhang, Xiao Zhang, Xiao-jun Wu
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引用次数: 1

摘要

目的探讨化疗联合自噬抑制剂对结肠癌细胞凋亡及钙调蛋白(CRT)表达的影响。方法以结肠癌细胞HCT116为研究对象。MTT法测定化疗药物奥沙利铂、5-Fu和SN-38的抑制率(IC50)。采用流式细胞术检测化疗前后HCT116细胞膜上CRT表达及细胞凋亡的变化。采用荧光免疫法检测化疗前后HCT116的CRT位置。采用Western blotting检测化疗药物对HCT116细胞自噬的影响。采用流式细胞术检测化疗药物联合自噬抑制剂氯喹(CQ)治疗前后HCT116膜上CRT表达及细胞凋亡的变化。结果奥沙利铂、5-Fu和SN38治疗12 h后,细胞凋亡率和CRT膜表达均升高,但差异无统计学意义。荧光免疫分析显示,奥沙利铂治疗后,CRT从细胞质转移到膜。Western blotting结果显示,奥沙利铂、5Fu和SN38均可诱导HCT116细胞自噬,CQ的加入可抑制细胞自噬。流式细胞术分析显示,化疗药物联合CQ治疗后,膜联蛋白V+细胞百分比和CRT膜表达均较高。奥沙利铂联合CQ治疗后,膜上CRT表达的上调幅度明显高于治疗前(P=0.027)。结论奥沙利铂联合CQ可提高HCT116细胞的凋亡率,上调细胞膜上CRT的表达。DOI: 10.11855 / j.issn.0577-7402.2016.04.03
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Influences of combination of chemotherapy and autophagy inhibitor on the calreticulin expression in colon cancer cells
Objective  To investigate the influence of chemotherapy combined with autophagy inhibitor on apoptosis and calreticulin (CRT) expression on colonic cancer cells. Methods  The colon cancer cells HCT116 were taken as the target in the present study. The inhibition rates (IC50) of chemotherapeutics oxaliplatin, 5-Fu and SN-38 were assessed by MTT assay. The changes in CRT expression on the membrane of HCT116 and apoptosis were determined with flow cytometry before and after treatment with chemotherapeutics. CRT location in HCT116 was detected by fluorescent immunoassay before and after treatment with chemotherapeutic agents. The influence on HCT116 autophagy was determined by Western blotting after treatment with these chemotherapeutic agents. The changes in CRT expression on HCT116 membrane and apoptosis were determined with flow cytometry before and after treatment with the chemotherapeutics combined with autophagy inhibitor chloroquine (CQ). Results  The ratio of apoptosis and membrane expression of CRT were elevated 12 hours after treatment with Oxaliplatin, 5-Fu and SN38, but without statistical significance. Fluorescent immunoassay showed a transposition of CRT from cytoplasm to the membrane after oxaliplatin treatment. Western blotting revealed that oxaliplatin, 5Fu and SN38 induced autophagy of HCT116 cells, and the autophagy was inhibited by the addition of CQ. Flow cytometric analysis indicated that the percentages of annexin V+ cells and membrane expression of CRT were higher after treatment with the chemotherapy agents combined with CQ. The upregulation of CRT expression on membrane was obviously higher after treatment with oxaliplatin combined with CQ than that before the treatment with these agents (P=0.027). Conclusion  Oxaliplatin combined with CQ may increase the apoptosis rate of HCT116 cells and upregulate CRT expression in the membrane. DOI: 10.11855/j.issn.0577-7402.2016.04.03
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解放军医学杂志
解放军医学杂志 Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
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