학술논문

Hepatitis B virus induces G1 phase arrest by regulating cell cycle genes in HepG2.2.15 cells
Document Type
article
Source
Virology Journal, Vol 8, Iss 1, p 231 (2011)
Subject
HepG2.2.15
HepG2
HBV
proliferation
cell cycle
Infectious and parasitic diseases
RC109-216
Language
English
ISSN
1743-422X
Abstract
Abstract Background To investigate the effect of HBV on the proliferative ability of host cells and explore the potential mechanism. Methods MTT, colony formation assay and tumourigenicity in nude mice were performed to investigate the effect of HBV on the proliferative capability of host cells. In order to explore the potential mechanism, cell cycle and apoptosis were analysed. The cell cycle genes controlling the G1/S phase transition were detected by immunohistochemistry, westernblot and RT-PCR. Results HepG2.2.15 cells showed decreased proliferation ability compared to HepG2 cells. G1 phase arrest was the main cause but was not associated with apoptosis. p53, p21 and total retinoblastoma (Rb) were determined to be up-regulated, whereas cyclinE was down-regulated at both the protein and mRNA levels in HepG2.2.15 cells. The phosphorylated Rb in HepG2.2.15 cells was decreased. Conclusions Our results suggested that HBV inhibited the capability of proliferation of HepG2.2.15 cells by regulating cell cycle genes expression and inducing G1 arrest.