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作 者:刘大闯[1,3] 陶陶[1] 许斌[1] 陈恕求[1] 刘春辉[1] 张磊[1] 卢凯[1] 陈明[1] 韩从辉[2,3]
机构地区:[1]东南大学附属中大医院泌尿外科,南京210009 [2]东南大学附属徐州市中心医院泌尿外科 [3]徐州医学院附属徐州临床学院泌尿外科
出 处:《中国男科学杂志》2014年第8期3-8,共6页Chinese Journal of Andrology
基 金:本课题受国家自然基金(81370849、81300472、81272557、81202034)、临床医学科技专项-新型临床诊疗技术攻关(BL2013032)、教育部博士点基金(20120092120071)、江苏省自然科学基金(BK2012336、BK2012647)、南京市科技发展项目(201201053)、东南大学新教师基本科研项目(3290002402)、江苏省普通高校研究生科研创新计划项目(CXZZ130133)和中央高校基本科研业务费专项资金资助资助
摘 要:目的:探讨mirR-361-5p在激素非依赖性前列腺癌细胞PC3中的表达和作用。方法采用qRT-PCR检测转染后的PC3中miRNA-361-5p的表达情况,用CCK-8和克隆形成实验检测转染后的PC3细胞增殖能力,流式细胞仪检测细胞周期和细胞凋亡的变化,Transwell实验检测细胞侵袭能力。结果 qRT-PCR检测结果显示PC3中miR-361-5p含量低,脂质体法有较高的转染效率。CCK-8与克隆形成实验表明在PC3中升高miR-361-5p能够抑制前列腺癌细胞的活性和增殖能力。流式细胞检测发现miR-361-5p可增加细胞阻滞在G0/G1期和凋亡的比例。Transwell实验中,转染miR-361-5p后细胞通过小室的数量明显减少。结论 miR-361-5p能够抑制PC3的增殖与侵袭能力,从而发挥抑癌的作用。Objective To investigate the effects of mirR-361-5p on bilogical behaviors of androgen-independent human prostate cancer cellsPC3. Methods The expression of miR-361-5p in PC3 cells after transfection was detected by qRT-PCR. Cell viability and proliferation of PC3 cells trasfected with miR-361-5p were measured by Cell Counting Kit-8(CCK-8) assay and colony formation assay. Cell cycle and apoptosis of PC3 cells transfected with miR-361-5p were analyzed by flow cytometry. The invasion ability of cell was evaluated by Transwell assay. Results The results of qRT-PCR showed that the expression of miR-361-5p in PC3 cells was low, indicating transfection efficiency was higher using liposome method. Overexpression of miR-361-5p significantly inhibited the proliferation of PC3 cells. Cell cycle analysis of PC3 cells transfected with miR-361-5p showed that cell number in G0/G1 phase was high and cell apoptosis number was low. MiR-361-5p significantly inhibited the number of cells migrated through Transwell chambers membrane. Conclusion These findings suggest that miR-361-5p may be a tumor suppressor miR in PC3 and it can inhibit the proliferation and invasion ability of androgen-independent human prostate cancer cells.
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