中华普通外科杂志
中華普通外科雜誌
중화보통외과잡지
CHINESE JOURNAL OF GENERAL SURGERY
2010年
10期
834-837
,共4页
夏荣龙%徐宗全%张瑞琴%陈孝平
夏榮龍%徐宗全%張瑞琴%陳孝平
하영룡%서종전%장서금%진효평
癌,肝细胞%细胞周期%HIF-1α基因%Tet-on基因表达系统
癌,肝細胞%細胞週期%HIF-1α基因%Tet-on基因錶達繫統
암,간세포%세포주기%HIF-1α기인%Tet-on기인표체계통
Carcinoma,hepatocellular%Cell cycles%Hypoxia-inducible factor-1α%Tet-on gene expression system
目的 探讨HIF-1α表达对肝癌细胞增殖和细胞周期的影响.方法 利用Tet-on基因表达系统调控肝癌细胞系HepG2中HIF-1α的表达,检测细胞周期和细胞增殖的变化.结果 酶切和DNA测序证实Tet-on基因表达系统反应质粒PTRE-HIF-1α构建成功.获得了受强力霉素调控、稳定表达HIF-1α的肝癌细胞.随着强力霉素浓度增加,hiF-1α基因表达增加,HIF-1α在体外明显增加HepG2细胞增殖活性;G0/G1期细胞指数减少,细胞增殖指数增多.RT-PCR检测结果表明,随着HIF-1α基因表达增加,Cyclin A mRNA表达增加(P<0.001),Cyclin D1和Cyclin E mRNA表达水平无明显变化(P>0.05).结论 HIF-1α基因在体外可以通过HIF-1α表达水平的增加而促进肝癌细胞增殖活性,通过CyclinA表达增加缩短了肝癌细胞增殖周期.
目的 探討HIF-1α錶達對肝癌細胞增殖和細胞週期的影響.方法 利用Tet-on基因錶達繫統調控肝癌細胞繫HepG2中HIF-1α的錶達,檢測細胞週期和細胞增殖的變化.結果 酶切和DNA測序證實Tet-on基因錶達繫統反應質粒PTRE-HIF-1α構建成功.穫得瞭受彊力黴素調控、穩定錶達HIF-1α的肝癌細胞.隨著彊力黴素濃度增加,hiF-1α基因錶達增加,HIF-1α在體外明顯增加HepG2細胞增殖活性;G0/G1期細胞指數減少,細胞增殖指數增多.RT-PCR檢測結果錶明,隨著HIF-1α基因錶達增加,Cyclin A mRNA錶達增加(P<0.001),Cyclin D1和Cyclin E mRNA錶達水平無明顯變化(P>0.05).結論 HIF-1α基因在體外可以通過HIF-1α錶達水平的增加而促進肝癌細胞增殖活性,通過CyclinA錶達增加縮短瞭肝癌細胞增殖週期.
목적 탐토HIF-1α표체대간암세포증식화세포주기적영향.방법 이용Tet-on기인표체계통조공간암세포계HepG2중HIF-1α적표체,검측세포주기화세포증식적변화.결과 매절화DNA측서증실Tet-on기인표체계통반응질립PTRE-HIF-1α구건성공.획득료수강력매소조공、은정표체HIF-1α적간암세포.수착강력매소농도증가,hiF-1α기인표체증가,HIF-1α재체외명현증가HepG2세포증식활성;G0/G1기세포지수감소,세포증식지수증다.RT-PCR검측결과표명,수착HIF-1α기인표체증가,Cyclin A mRNA표체증가(P<0.001),Cyclin D1화Cyclin E mRNA표체수평무명현변화(P>0.05).결론 HIF-1α기인재체외가이통과HIF-1α표체수평적증가이촉진간암세포증식활성,통과CyclinA표체증가축단료간암세포증식주기.
Objective To investigate the effects of HIF-1α expression regulated by Tet-on gene expression system on cell proliferation and cell cycle of hepatoma cells in vitro. Methods The change of human hepatocellular carcinoma cell lines HepG2 cell cycle and cell proliferation was measured after HIF-1 α expression of HepG2 in vitro was regulated by Tet-on expression system. Results Amplified products were confirmed as the cDNA of HIF-1α by DNA sequencing, and pTRE-HIF-1α obtained by edonuclease digestion,capable of expression in HepG2 Tet-on cells. After being incubated under different concentrations of doxycycline for 48 h, MTT assays showed that up-regulation of HIF-1α expression increased HepG2 cell proliferation activities. The cell index of S and G2/M phase was significantly higher and that of G0/G1 phase reduced with the increasing concentrations of doxycycline. The mRNA expression of Cyclin A increased with the increasing concentrations of doxycycline ( P < 0. 001 ), CyclinD1 and CyclinE did not change ( P >0. 05). Conclusion HIF-1 α gene promotes cell proliferation and cell cycle of hcpatoma cells in vitro, and this effects increased with the increasing of HIF-1α expression possibly through influencing the expression of CyclinA.