Malignant transformation of the cultured human hepatocytes induced by hepatitis C virus core protein

: Background/Aim: Hepatitis C virus core protein (HCV‐C) has been known to play an important role in hepatocarcinogenesis. But, up to now there is no certain evidence in pathomorphology directly supporting this standpoint. In this study, a human hepatocytes model expressing HCV‐C was established for...

Full description

Saved in:
Bibliographic Details
Published inLiver international Vol. 25; no. 1; pp. 141 - 147
Main Authors Shan, Yu, Chen, Xi-gu, Huang, Bing, Hu, An-bin, Xiao, Dong, Guo, Zhong-min
Format Journal Article
LanguageEnglish
Published Oxford, UK Munksgaard International Publishers 01.02.2005
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:: Background/Aim: Hepatitis C virus core protein (HCV‐C) has been known to play an important role in hepatocarcinogenesis. But, up to now there is no certain evidence in pathomorphology directly supporting this standpoint. In this study, a human hepatocytes model expressing HCV‐C was established for investigating the influence of HCV‐C on hepatocytes biological properties. Methods: The HCV‐C expression plasmid, PcDNA3‐C, was transfected into Chang‐liver cells to establish HCV‐C expressing cells. Proliferation rate and variation index of DNA content of these cells were measured by MTT and FCM. The malignant transformation of these cells was observed by electron microscope. Furthermore, these cells were subcutaneous injected into nude mice to observed their tumor genesis. Results: Proliferation rate and variation index of DNA content of these cells markedly increased. 10/10 of BALB/c‐nu/nu nude mice generated tumors at 3 weeks after subcutaneous inoculation of the HCV‐C expressing cells. And, histological structure of the tumors coincided with that of hepatocarcinoma. Conclusions: The HCV‐C may play a key role in hepatocarcinogenesis resulting from HCV infection.
Bibliography:ArticleID:LIV999
ark:/67375/WNG-XQSS4WL5-N
istex:6A16EEA4CAA2AB7AC9BA10CBC15A042C6DCAD99A
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1478-3223
1478-3231
DOI:10.1111/j.1478-3231.2005.0999.x