In situ detection of TGF betas, TGF beta receptor II mRNA and telomerase activity in rat cholangiocarcinogenesis

Initial report on the in situ examination of the mRNA expression of transforming growth factor betas (TGFbetas), TGFbeta type II receptor (TbetaRII) and telomerase activity in the experimental rat liver tissue during cholangiocarcinogenesis. Rat liver cholangiocarcinogenesis was induced by 3'-m...

Full description

Saved in:
Bibliographic Details
Published inWorld journal of gastroenterology : WJG Vol. 9; no. 3; pp. 590 - 594
Main Authors Lu, Jian-Ping, Mao, Jian-Qun, Li, Ming-Sheng, Lu, Shi-Lun, Hu, Xi-Qi, Zhu, Shi-Neng, Nomura, Shintaro
Format Journal Article
LanguageEnglish
Published United States Department of Pathology, Medical Center of Fudan University (Former Shanghai Medical University), Shanghai 200032,China. Max-Planck-Institute for Cell Biology, Ladenburg 68526,Germany%Department of Pathology, Medical Center of Fudan University,(Former Shanghai Medical University), Shanghai 200032, China%Department of Pathology,Osaka University,School of Medicine,Fukita 565,Japan 01.03.2003
Baishideng Publishing Group Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Initial report on the in situ examination of the mRNA expression of transforming growth factor betas (TGFbetas), TGFbeta type II receptor (TbetaRII) and telomerase activity in the experimental rat liver tissue during cholangiocarcinogenesis. Rat liver cholangiocarcinogenesis was induced by 3'-methyl 4-dimethylazobenzene (3'Me-DAB). In situ hybridization was used to examine the TGFbetas) and TGFbeta type II receptor (TbetaRII) mRNA, in situ TRAP was used to check the telomerase activity in the tissue samples. There was no TGFbetas, TbetaRII mRNA expression or telomerase activity in the control rat cholangiocytes. The expression of TGFbeta1, TbetaRII was increased in regenerative, hyperplastic, dysplastic cholangiocytes and cholangiocarcinoma (CC) cells. The expression of TGFbeta2 mRNA was observed in only a part of hyperplastic, dysplastic cholangiocytes. TGFbeta3 expression was very weak, only in hyperplastic lesion. There was positive telomerase activity in the regenerative, hyperplastic, dysplastic cholangiocytes, and CC cells. Stroma fibroblasts of these lesions also showed positive TGFbetas, TbetaRII mRNA expression and telomerase activity. There were TGFbetas, TbetaRII expression and telomerase activity in hyperplastic, dysplastic cholangiocytes, cholangiocarcinoma cells as well as in stroma fibroblasts during cholangiocarcinogenesis. Their expression or activity is important in cholangiocarcinogenesis andstroma formation.
Bibliography:Correspondence to: Jian-Ping Lu, Ph.D. Max-Planck-Institute for Cell Biology, Ladenburg 68526, Germany. lu_jp@hotmail.com
Telephone: +49-6203-106-208 Fax: +49-6203-106-122
Author contributions: All authors contributed equally to the work.
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v9.i3.590