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Gene Transfer of Pigment Epithelium-Derived Factor Suppresses Tumor Growth and Angiogenesis in a Hepatoblastoma Xenograft Model

Authors
 Marybeth Browne  ;  Veronica Stellmach  ;  Mona Cornwell  ;  Chuhan Chung  ;  Jennifer A Doll  ;  Eun-Jig Lee  ;  J Larry Jameson  ;  Marleta Reynolds  ;  Riccardo A Superina  ;  Lisa P Abramson  ;  Susan E Crawfor 
Citation
 PEDIATRIC RESEARCH, Vol.60(3) : 282-287, 2006 
Journal Title
 PEDIATRIC RESEARCH 
ISSN
 0031-3998 
Issue Date
2006
MeSH
Animals ; Cell Line, Tumor ; Disease Models, Animal ; Eye Proteins/genetics* ; Eye Proteins/metabolism ; Female ; Genetic Therapy* ; Hepatoblastoma/therapy* ; Humans ; Liver Neoplasms/therapy* ; Mice ; Neovascularization, Pathologic/therapy* ; Nerve Growth Factors/genetics* ; Nerve Growth Factors/metabolism ; Serpins/genetics* ; Serpins/metabolism ; Transplantation, Heterologous
Abstract
Normal hepatocytes express pigment epithelium-derived factor (PEDF), an endogenous antiangiogenic factor. We hypothesized that decreased PEDF expression may be one mechanism driving hepatoblastoma growth, and in vivo gene transfer of PEDF could suppress neovascularization and limit tumor growth. PEDF functional activity was determined in vitro using endothelial cell migration assays and in vivo using a subcutaneous tumor model. HUH-6 human hepatoblastoma tumors were treated with hybrid adenoviral/adeno-associated viral expression vectors for PEDF (Hyb-PEDF, n = 4) or β-galactosidase (Hyb-βgal, n = 4) daily for 4 d. Mitotic figures, microvascular density (MVD), PEDF, and VEGF expression were assessed. Hyb-PEDF treatment inhibited in vivo tumor growth (p < 0.008) and decreased MVD (p < 0.001), the number of mitotic figures (p < 0.001), and VEGF expression when compared with Hyb-βgal-treated tumors. HUH-6 expression of PEDF was dramatically reduced when cultured under hypoxic conditions and also when grown in vivo, and the addition of neutralizing anti-PEDF antibody increased the already high baseline angiogenic activity of the HUH-6 cell secretions in vitro (p < 0.04). PEDF is an important endogenous regulator of the liver vasculature. Augmenting intra-tumoral PEDF levels inhibits tumor growth by reducing angiogenesis and VEGF expression. Potent inhibitors of angiogenesis, such as PEDF, may be an effective alternative treatment for children with hepatoblastoma.
Full Text
http://www.nature.com/pr/journal/v60/n3/full/pr2006238a.html
DOI
10.1203/01.pdr.0000232789.86632.91
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Lee, Eun Jig(이은직) ORCID logo https://orcid.org/0000-0002-9876-8370
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/109983
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