生物技术通讯
生物技術通訊
생물기술통신
LETTERS IN BIOTECHNOLOGY
2014年
6期
783-786
,共4页
南雪%曾泉%吕洋%姚海雷%陈琳%岳文%裴雪涛
南雪%曾泉%呂洋%姚海雷%陳琳%嶽文%裴雪濤
남설%증천%려양%요해뢰%진림%악문%배설도
miRNA%miR-155%肝癌%细胞增殖
miRNA%miR-155%肝癌%細胞增殖
miRNA%miR-155%간암%세포증식
miRNA%miR-155%hepatocellular carcinoma%cell proliferation
目的:在肝癌细胞系中过表达miR-155,研究其对肝癌细胞增殖的影响。方法:将pcDNA3.0-miR-155表达载体瞬时转染Huh7.5.1及Hcclm3肝癌细胞系,通过实时定量PCR技术对miR-155在转录水平的表达进行检测,采用CCK8法及克隆形成实验检测miR-155过表达后对Huh7.5.1及Hcclm3肝癌细胞系增殖的影响。结果:转染细胞后72 h,经实时定量PCR检测,Huh7.5.1及Hcclm3肝癌细胞中成熟miR-155的表达分别上调约431及16倍(P<0.01),说明其能有效高表达;CCK8法及克隆形成实验结果显示,miR-155能够明显促进肝癌细胞增殖(P<0.01)。结论:pcDNA3.0-miR-155转染Huh7.5.1及Hcclm3肝癌细胞系后能高效表达成熟miR-155,同时证明过表达miR-155能使肝癌细胞的增殖受到非常明显的促进。
目的:在肝癌細胞繫中過錶達miR-155,研究其對肝癌細胞增殖的影響。方法:將pcDNA3.0-miR-155錶達載體瞬時轉染Huh7.5.1及Hcclm3肝癌細胞繫,通過實時定量PCR技術對miR-155在轉錄水平的錶達進行檢測,採用CCK8法及剋隆形成實驗檢測miR-155過錶達後對Huh7.5.1及Hcclm3肝癌細胞繫增殖的影響。結果:轉染細胞後72 h,經實時定量PCR檢測,Huh7.5.1及Hcclm3肝癌細胞中成熟miR-155的錶達分彆上調約431及16倍(P<0.01),說明其能有效高錶達;CCK8法及剋隆形成實驗結果顯示,miR-155能夠明顯促進肝癌細胞增殖(P<0.01)。結論:pcDNA3.0-miR-155轉染Huh7.5.1及Hcclm3肝癌細胞繫後能高效錶達成熟miR-155,同時證明過錶達miR-155能使肝癌細胞的增殖受到非常明顯的促進。
목적:재간암세포계중과표체miR-155,연구기대간암세포증식적영향。방법:장pcDNA3.0-miR-155표체재체순시전염Huh7.5.1급Hcclm3간암세포계,통과실시정량PCR기술대miR-155재전록수평적표체진행검측,채용CCK8법급극륭형성실험검측miR-155과표체후대Huh7.5.1급Hcclm3간암세포계증식적영향。결과:전염세포후72 h,경실시정량PCR검측,Huh7.5.1급Hcclm3간암세포중성숙miR-155적표체분별상조약431급16배(P<0.01),설명기능유효고표체;CCK8법급극륭형성실험결과현시,miR-155능구명현촉진간암세포증식(P<0.01)。결론:pcDNA3.0-miR-155전염Huh7.5.1급Hcclm3간암세포계후능고효표체성숙miR-155,동시증명과표체miR-155능사간암세포적증식수도비상명현적촉진。
Objective: To study the effect of miR-155 overexpression on hepatocellular carcinoma cell prolifera?tion. Methods: pcDNA3.0-miR-155 was transiently transfected into Huh7.5.1 and Hcclm3 hepatocellular carcino?ma cell lines. RT-PCR assay was used to access the transcription level of miR-155. CCK8 assay and colony-form?ing unit assay were used to evaluate the effect of miR-155 overexpression on Huh7.5.1 and Hcclm3 cell prolifera?tion. Results: miR-155 could be highly efficient expressed 72 h post transfection, and the expression level was accordingly upregulated 431 and 16 folds respectively(P<0.01). CCK8 assay and colony-forming unit assay also showed that miR-155 could obviously stimulate hepatocellular carcinoma cell proliferation(P<0.01). Conclusion:miR-155 can be highly expressed in Huh7.5.1 and Hcclm3 hepatocellular carcinoma cell lines via pcDNA3.0-miR-155 transfection. Meanwhile, miR-155 overexpression can obviously promote hepatocellular carcinoma cell pro?liferation.