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作 者:王顺业 徐瑞容[1] 黄红铭[1] 丁润生[1] 那文秀 张立娜[1]
出 处:《交通医学》2015年第1期4-6,共3页Medical Journal of Communications
基 金:江苏省自然科学基金资助项目(BK2011388);南通大学研究生创新课题计划(YKC13082)
摘 要:目的:探究miR-17-3P对多发性骨髓瘤(MM)细胞增殖的影响。方法:通过实时荧光定量聚合酶链反应测定miR-17-3P在MM细胞系RPMI 8226、U266和KM3及正常人骨髓细胞中的表达情况。合成miR-17-3P模拟物和抑制物,分别转染U266细胞,采用MTT法测细胞活力,PI染色流式细胞仪测细胞周期,观察U266细胞增殖情况。结果:MM细胞株RPMI8226、U266、KM3中miR-17-3P相对表达量均明显高于正常人骨髓细胞;利用模拟物上调miR-17-3P后,U266的细胞活力较对照组明显提高,48h时作用效果最为显著;相反,下调miR-17-3P后,U266的细胞活力降低;上调miR-17-3P后,G1期细胞比例较对照组有所减少,S期细胞比例明显增多;相反,下调miR-17-3P后,细胞多被阻滞在G1期。结论:Mi R-17-3P可能促进多发性骨髓瘤细胞增殖。Objective:To study the effection of miR-17-3P on cell proliferation of multiple myeloma. Methods:The expressions of miR-17-3P in MM cell lines RPMI8226,U266,KM3 and the healthy controls were measured by real-time PCR. After the construction of the angomiR-17-3P and antagomiR-17-3P, they were transfected into U266, the cell proliferation was measured by MTT, growth curve was drawn, and then the cell cycle was measured with PI stained by flow cytometry. Results: AngomiR-17-3P mimics could increase the expression of corresponding miRNA, promote the proliferation of MM cells; AntagomiR-17-3P inhibitor could reduce the expression of corresponding miRNA and suppress the proliferation of MM cells. Conclusion:MiR-17-3P could promote the cell proliferation of multiple myeloma.
关 键 词:多发性骨髓瘤 U266细胞 实时荧光定量聚合酶链反应 流式细胞仪检测 MTT比色法
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