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[细胞周期对肝癌细胞端粒酶活性的影响及其与乙型肝炎病毒复制的关系]

[Effect of cell cycle on telomerase activity of hepatoma cells and its relationship with replication of hepatitis B virus].

作者信息

Yan Shao-Nan, Deng Bin, Gong Zuo-Jiong

机构信息

Department of Infectious Disease, Renmin Hospital, Wuhan University, Wuhan, Hubei, PR China.

出版信息

Ai Zheng. 2003 May;22(5):504-7.

Abstract

BACKGROUND & OBJECTIVE: Previous studies have shown that the expression of telomerase activity is closely correlated with the formation and development of tumor cells. Furthermore, the cell cycle is associated with hepatitis B virus (HBV) replication level and telomerase activity. For further study their relationship, this experiment was designed to investigate the effect of serum deprivation or all-trans-retinoic acid(RA)on cell cycle of human hepatoma cells transfected by HBV DNA (HepG2 cell line) and the associations of cell cycle with telomerase activity and HBV replication.

METHODS

Human hepatoma HepG2 cells were respectively treated with serum deprivation or RA. Cell cycle was analyzed using flow cytometry. Telomerase activity was determined quantitatively by TRAP-PCR-ELISA. HBV-DNA in culture media was determined using quantitative PCR and semiquantitative dot blot hybridization assay. HBsAg and HBeAg in cell culture media were measured using quantitative ELISA.

RESULTS

RA treatment or serum deprivation inhibited the proliferation of HepG2 cells and the cells were arrested at G(0)/G(1) phase. The percentages of G(0)/G(1) phase of RA group and serum deprivation were 68.3% and 65.2%, respectively, while that of control group was 43.1% (P< 0.01). The levels of telomerase activity also significantly decreased. The absorbance values that represented the telomerase activity of RA group and serum deprivation group were 0.32 and 0.41, respectively, while that of control group was 1.34(P< 0.01). In addition,HBV replication of HepG2 cells remarkably increased, which was shown as high products of HBV-DNA, HBsAg and HBeAg in culture media of RA group and serum deprivation group. The contents of HBV DNAs were 4.4x10(6), 5.1x10(6), and 1.2x10(6) copies/ml in RA group, serum deprivation group, and control group, respectively(P< 0.01). The values of P/N of HBsAg were 3.5, 3.7, and 1.3 in RA group, serum deprivation group, and control group, respectively (P< 0.01). The values of P/N of HBeAg were 19.8, 22.5, and 13.4 in RA group, serum deprivation group, and control group, respectively (P< 0.01).

CONCLUSION

Telomerase expression was associated with cell cycle in HepG2 cells. Telomerase was mainly expressed in S phase of cell cycle. HBV replication was also closely correlated with cell cycle, which increased in quiescent hepatocytes and decreased in proliferating hepatocytes.

摘要

背景与目的

既往研究表明,端粒酶活性的表达与肿瘤细胞的形成和发展密切相关。此外,细胞周期与乙型肝炎病毒(HBV)复制水平及端粒酶活性相关。为进一步研究它们之间的关系,本实验旨在探讨血清剥夺或全反式维甲酸(RA)对转染HBV DNA的人肝癌细胞(HepG2细胞系)细胞周期的影响,以及细胞周期与端粒酶活性和HBV复制的关系。

方法

人肝癌HepG2细胞分别用血清剥夺或RA处理。采用流式细胞术分析细胞周期。通过TRAP-PCR-ELISA法定量测定端粒酶活性。采用定量PCR和半定量斑点杂交法检测培养基中的HBV-DNA。采用定量ELISA法检测细胞培养基中的HBsAg和HBeAg。

结果

RA处理或血清剥夺抑制了HepG2细胞的增殖,细胞停滞于G(0)/G(1)期。RA组和血清剥夺组G(0)/G(1)期细胞百分比分别为68.3%和65.2%,而对照组为43.1%(P<0.01)。端粒酶活性水平也显著降低。代表RA组和血清剥夺组端粒酶活性的吸光度值分别为0.32和0.41,而对照组为1.34(P<0.01)。此外,HepG2细胞的HBV复制显著增加,表现为RA组和血清剥夺组培养基中HBV-DNA、HBsAg和HBeAg的高产量。RA组、血清剥夺组和对照组HBV DNA含量分别为4.4×10(6)、5.1×10(6)和1.2×10(6)拷贝/ml(P<0.01)。RA组、血清剥夺组和对照组HBsAg的P/N值分别为3.5、3.7和1.3(P<0.01)。RA组、血清剥夺组和对照组HBeAg的P/N值分别为19.8、22.5和13.4(P<0.01)。

结论

端粒酶表达与HepG2细胞的细胞周期相关。端粒酶主要在细胞周期的S期表达。HBV复制也与细胞周期密切相关,在静止肝细胞中增加,在增殖肝细胞中减少。

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