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作 者:蒲猛 汪建林[1] 黄启科[1] 赵戈[1] 夏聪聪[1] 何大立 杨针 陶开山[1] PU Meng WANG Jian-lin HUANG Qi-ke ZHAO Ge XIA Cong-cong HE Da-li YANG Zhen TAO KM-shan(Department of Hepatobiliary Surgery, Xijing Hospital, Fourth Military Mech'cal University, Xi'nn, Shaanxi, 710032, China)
机构地区:[1]第四军医大学西京医院肝胆胰脾外科,陕西西安710032
出 处:《现代生物医学进展》2017年第12期2201-2204,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(81670593;81272648)
摘 要:目的:研究Bub1基因在肝癌中的表达以及对肝癌细胞系MHCC97-H增殖、周期和凋亡的影响。方法:利用RNA干扰技术下调肝癌细胞系MHCC97-H中Bub1的表达;qRT-PCR和Western Blot分别检测Bub1在mRNA和蛋白水平表达的变化;CCK-8实验检测肿瘤细胞增殖能力的改变;流式细胞术检测细胞周期和凋亡的变化。结果:qRT-PCR和Western Blot结果显示si-Bub1能够成功下调Bub1的表达;下调Bub1后肝癌MHCC97-H细胞的增殖能力下降(P<0.05),细胞的凋亡比例升高(P<0.05),细胞发生S期阻滞。结论:Bub1基因在肝癌中高表达,下调Bub1的表达后能够降低肝癌细胞的增殖能力,促进细胞凋亡,诱导细胞发生S期阻滞。Objective: To study the expression of Bubl in hepatocellular carcinoma (HCC) and its effect on the cell proliferation, cell cycle and apoptosis in hepatocellular carcinoma cell line MHCC97-H. Methods: Bubl was down-regulated by small interfering RNA (siRNA) in MHCC97-H. qRT-PCR and Western blot were used to determine the expression of mRNA and protein. CCK-8 assay was performed to evaluate the proliferation ability. Apoptosis and cell cycles were determined by flow cytometry. Rosults: qRT-PCR and Western blot showed that si-Bubl group displayed a low expression ofBubl. Down-regulated of Bubl by siRNA significantly inhibited the cell proliferation (P〈0.05), Cell cycle had changed and increased the cell apoptosis rates (P〈0.05). Conclusion: Bubl was highly expressed in hepatocellular carcinoma and down-regnlating the expression of Bubl couldreduce the proliferation of hepatocellular carcinoma cells and affect the cell cycle and apoptosis of HCC.
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