中国男科学杂志
中國男科學雜誌
중국남과학잡지
CHINESE JOURNAL OF ANDROLOGY
2014年
8期
3-8
,共6页
刘大闯%陶陶%许斌%陈恕求%刘春辉%张磊%卢凯%陈明%韩从辉
劉大闖%陶陶%許斌%陳恕求%劉春輝%張磊%盧凱%陳明%韓從輝
류대틈%도도%허빈%진서구%류춘휘%장뢰%로개%진명%한종휘
前列腺肿瘤%miR-361-5p%细胞增殖%肿瘤侵袭力
前列腺腫瘤%miR-361-5p%細胞增殖%腫瘤侵襲力
전렬선종류%miR-361-5p%세포증식%종류침습력
prostatic neoplasms%miR-361-5p%cell proliferation%invasiveness
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。
目的:探討mirR-361-5p在激素非依賴性前列腺癌細胞PC3中的錶達和作用。方法採用qRT-PCR檢測轉染後的PC3中miRNA-361-5p的錶達情況,用CCK-8和剋隆形成實驗檢測轉染後的PC3細胞增殖能力,流式細胞儀檢測細胞週期和細胞凋亡的變化,Transwell實驗檢測細胞侵襲能力。結果 qRT-PCR檢測結果顯示PC3中miR-361-5p含量低,脂質體法有較高的轉染效率。CCK-8與剋隆形成實驗錶明在PC3中升高miR-361-5p能夠抑製前列腺癌細胞的活性和增殖能力。流式細胞檢測髮現miR-361-5p可增加細胞阻滯在G0/G1期和凋亡的比例。Transwell實驗中,轉染miR-361-5p後細胞通過小室的數量明顯減少。結論 miR-361-5p能夠抑製PC3的增殖與侵襲能力,從而髮揮抑癌的作用。
목적:탐토mirR-361-5p재격소비의뢰성전렬선암세포PC3중적표체화작용。방법채용qRT-PCR검측전염후적PC3중miRNA-361-5p적표체정황,용CCK-8화극륭형성실험검측전염후적PC3세포증식능력,류식세포의검측세포주기화세포조망적변화,Transwell실험검측세포침습능력。결과 qRT-PCR검측결과현시PC3중miR-361-5p함량저,지질체법유교고적전염효솔。CCK-8여극륭형성실험표명재PC3중승고miR-361-5p능구억제전렬선암세포적활성화증식능력。류식세포검측발현miR-361-5p가증가세포조체재G0/G1기화조망적비례。Transwell실험중,전염miR-361-5p후세포통과소실적수량명현감소。결론 miR-361-5p능구억제PC3적증식여침습능력,종이발휘억암적작용。
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.