[Expression of Ang2 and Tie2 and their relation with the angiogenesis of hepatocellular carcinoma in rats]

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2006 Aug;31(4):523-7.
[Article in Chinese]

Abstract

Objective: To investigate the relationship between the expression of Ang2, Tie2 and the angiogenesis of hepatocellular carcinoma in rats.

Methods: Thirty-eight healthy male rats were randomly divided into 3 groups: 5 rats in the control group; 25 rats in the experimental group were equally divided into 5-day, 10-day, 15-day, 20-day, and 25-day groups; the other 8 rats were used as the supplement of the experimental group. An allogenic transplanted rat model of CBRH-7919 hepatocellular carcinoma in situ was established by immunosuppression. The expressions of Ang2 and Tie2 were detected by immunohistochemical staining in cancerous tissues of different developmental stages and liver tissues of the control group. At the same time, microvessel density was determined by anti-CD31 immunohistochemical staining.

Results: CBRH-7919 hepatocellular carcinoma models were successfully set up in 24 rats. The expression level of Ang2 and Tie2 in cancerous tissues was much higher than that of liver tissues of the control group (P <0.05). The overexpression of Ang2 was pristine and continuous in different developmental stages. The expressions of Ang2 and Tie2 positively correlated with microvessal density in hepatocellular carcinoma (P<0.05).

Conclusion: The up-regulation of Ang2 and Tie2 may play important roles in the angiogenesis of hepatocellular carcinoma. Ang2 may participate in the start of angiogenesis of hepatocellular carcinoma.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiopoietin-2 / biosynthesis*
  • Angiopoietin-2 / genetics
  • Animals
  • Liver Neoplasms, Experimental / blood supply*
  • Liver Neoplasms, Experimental / metabolism*
  • Male
  • Neovascularization, Pathologic*
  • RNA, Messenger / genetics
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Receptor, TIE-2 / biosynthesis*
  • Receptor, TIE-2 / genetics

Substances

  • Angiopoietin-2
  • RNA, Messenger
  • Receptor, TIE-2