中国男科学杂志
中國男科學雜誌
중국남과학잡지
CHINESE JOURNAL OF ANDROLOGY
2014年
12期
7-10
,共4页
付振宇%张鸽%黄玉华%严春寅%俞江%孙利国%陈永昌%缪瑜%张杰
付振宇%張鴿%黃玉華%嚴春寅%俞江%孫利國%陳永昌%繆瑜%張傑
부진우%장합%황옥화%엄춘인%유강%손리국%진영창%무유%장걸
微RNAs%前列腺肿瘤%细胞系%肿瘤%缺氧诱导因子1%α亚基%细胞增殖%细胞凋亡
微RNAs%前列腺腫瘤%細胞繫%腫瘤%缺氧誘導因子1%α亞基%細胞增殖%細胞凋亡
미RNAs%전렬선종류%세포계%종류%결양유도인자1%α아기%세포증식%세포조망
microRNAs%prostatic neoplasms%cell line%tumor%hypoxia inducible factor 1%alpha subunit%cell proliferation%apoptosis
目的:探讨沉默缺氧诱导因子-lα(hypoxia inducible factor-lα,HIF-lα)基因对前列腺癌PC3细胞生长增殖及细胞凋亡的影响。方法实验分为PC3组(空白对照组)、PC3+NC siRNA组(阴性对照组)和PC3+HIF-lαsiRNA组(干扰组)。使用经过筛选证实有效的HIF-lα-siRNA序列和阴性对照NC-siRNA序列,经脂质体Lipofectamine 2000转染PC3细胞。采用CCK-8法检测转染后96h内各组细胞的生长增殖情况,流式细胞仪检测转染后48h各组细胞的凋亡率。结果 PC3+HIF-lαsiRNA组肿瘤抑制率高于PC3+NC siRNA组,尤以转染后第48h表现得较为明显;在第48h,PC3+HIF-lαsiRNA组细胞存活率明显低于PC3组和PC3+NCsiRNA组(P<0.01)。转染后第48h,干扰组细胞凋亡率为(11.2±1.13)%,PC3组和PC3+NC siRNA组细胞凋亡率分别为(2.4±0.26)%和(2.5±0.36)%,干扰组细胞凋亡率显著高于两对照组(P<0.01)。结论沉默HIF-lα基因能抑制前列腺癌PC3细胞的生长,诱导癌细胞凋亡,发挥抗肿瘤作用。
目的:探討沉默缺氧誘導因子-lα(hypoxia inducible factor-lα,HIF-lα)基因對前列腺癌PC3細胞生長增殖及細胞凋亡的影響。方法實驗分為PC3組(空白對照組)、PC3+NC siRNA組(陰性對照組)和PC3+HIF-lαsiRNA組(榦擾組)。使用經過篩選證實有效的HIF-lα-siRNA序列和陰性對照NC-siRNA序列,經脂質體Lipofectamine 2000轉染PC3細胞。採用CCK-8法檢測轉染後96h內各組細胞的生長增殖情況,流式細胞儀檢測轉染後48h各組細胞的凋亡率。結果 PC3+HIF-lαsiRNA組腫瘤抑製率高于PC3+NC siRNA組,尤以轉染後第48h錶現得較為明顯;在第48h,PC3+HIF-lαsiRNA組細胞存活率明顯低于PC3組和PC3+NCsiRNA組(P<0.01)。轉染後第48h,榦擾組細胞凋亡率為(11.2±1.13)%,PC3組和PC3+NC siRNA組細胞凋亡率分彆為(2.4±0.26)%和(2.5±0.36)%,榦擾組細胞凋亡率顯著高于兩對照組(P<0.01)。結論沉默HIF-lα基因能抑製前列腺癌PC3細胞的生長,誘導癌細胞凋亡,髮揮抗腫瘤作用。
목적:탐토침묵결양유도인자-lα(hypoxia inducible factor-lα,HIF-lα)기인대전렬선암PC3세포생장증식급세포조망적영향。방법실험분위PC3조(공백대조조)、PC3+NC siRNA조(음성대조조)화PC3+HIF-lαsiRNA조(간우조)。사용경과사선증실유효적HIF-lα-siRNA서렬화음성대조NC-siRNA서렬,경지질체Lipofectamine 2000전염PC3세포。채용CCK-8법검측전염후96h내각조세포적생장증식정황,류식세포의검측전염후48h각조세포적조망솔。결과 PC3+HIF-lαsiRNA조종류억제솔고우PC3+NC siRNA조,우이전염후제48h표현득교위명현;재제48h,PC3+HIF-lαsiRNA조세포존활솔명현저우PC3조화PC3+NCsiRNA조(P<0.01)。전염후제48h,간우조세포조망솔위(11.2±1.13)%,PC3조화PC3+NC siRNA조세포조망솔분별위(2.4±0.26)%화(2.5±0.36)%,간우조세포조망솔현저고우량대조조(P<0.01)。결론침묵HIF-lα기인능억제전렬선암PC3세포적생장,유도암세포조망,발휘항종류작용。
Objective To investigate the effects of hypoxia inducible factor-lα gene silencing with siRNA on the proliferation and apoptosis of human prostate cancer cells. Methods PC3 cells were divided into three groups such as PC3 group, PC3+ NC siRNA group and PC3 + HIF-lα siRNA group. Cells in each group were transfected with HIF-lα-siRNA using Lipofectamine 2000. CCK-8 test was used to measure the proliferation of PC3 cells. Flow cytometer was used to measure cell apoptosis. Results Survival rate of PC3+HIF-lα siRNA group was significantly lower than that of other two control groups at 24h, 48h, 72h and 96h after transfection (P<0.01). The interference effect reached its peak at 48h after transfection. The rates of cell apoptosis of PC3 + HIF-lα siRNA group, PC3 group, PC3+ NC siRNA group at 48h after transfection were (11.2±1.13)%,(2.4±0.26)% and (2.5±0.36)% respectively; The apoptosis rates of PC3 + HIF-lαsiRNA group was higher than that of the others (P<0.01). Conclusion Silencing HIF-lα gene can effectively inhibit cell proliferation, and induce the apoptosis of PC3 cells.