PEDF effectively decreases VEGF to PEDF messenger RNA ratio of the inner edge of rat hepatocellular carcinoma induced by diethyl nitrosamine - an "in vivo" study

Hepatogastroenterology. 2012 Jul-Aug;59(117):1484-90. doi: 10.5754/hge11543.

Abstract

Background/aims: Hepatocellular carcinoma (HCC) is hypervascular. Pigment epithelial derived factor (PEDF), a potent angiogenic inhibitor, usually coexists with the stimulator, vascular endothelial growth factor (VEGF). To assess the treatment effect of PEDF on growing HCCs we conducted this study.

Methodology: Pathogen-free male LEW/SsN rats (n=150 in 5 groups), group A as control, groups B, C, D and E were given diethyl nitrosamine (DEN) to induce HCC. Group C received intraperitoneal injection (i.p.) of PEDF (0.3mg/kg/day) since induction. Group D received i.p. of PEDF (0.3mg/kg/day) since 18th week (wk). Group E received i.p. of normal saline. We examined VEGF mRNA and PEDF mRNA of livers of group A and 3 different areas (advancing edge, inner edge and central area) of HCC of other 4 groups at 24th wk.

Results: Tumor weight and metastasis score of group C were significantly lower (p=0.026). Comparing among 5 groups, the ratio of VEGF/PEDF mRNA of inner edge of HCC of group C and D were significantly lower (p=0.002 and p=0.011). By multivariate analysis, the difference of group C remains significant (p=0.030).

Conclusions: PEDF significantly suppresses rat hepatocarcinogenesis if given simultaneously since cancer induction. The significant decrease of VEGF/PEDF mRNA is at the inner edge of HCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinoma, Hepatocellular / chemically induced
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / metabolism*
  • Carcinoma, Hepatocellular / pathology*
  • Diethylnitrosamine
  • Eye Proteins / metabolism*
  • Eye Proteins / pharmacology*
  • Eye Proteins / therapeutic use
  • Liver Neoplasms, Experimental / chemically induced
  • Liver Neoplasms, Experimental / drug therapy
  • Liver Neoplasms, Experimental / metabolism*
  • Liver Neoplasms, Experimental / pathology*
  • Male
  • Multivariate Analysis
  • Neoplasm Metastasis
  • Nerve Growth Factors / metabolism*
  • Nerve Growth Factors / pharmacology*
  • Nerve Growth Factors / therapeutic use
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Lew
  • Serpins / metabolism*
  • Serpins / pharmacology*
  • Serpins / therapeutic use
  • Statistics, Nonparametric
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Eye Proteins
  • Nerve Growth Factors
  • RNA, Messenger
  • Serpins
  • Vascular Endothelial Growth Factor A
  • pigment epithelium-derived factor
  • Diethylnitrosamine