Up-regulation of vascular endothelial growth factor/vascular permeability factor in mouse skin carcinogenesis correlates with malignant progression state and activated H-ras expression levels

Cancer Res. 1996 Dec 1;56(23):5391-6.

Abstract

Angiogenesis is a crucial process for tumor growth and metastasis regulated by the balance of positive and negative factors. Vascular endothelial growth factor (VEGF/VPF) is a specific mitogen for endothelial cells that has been shown to be overexpressed in a variety of tumors and other inflammatory diseases. To analyze the implication of VEGF/VPF during tumorigenesis, we have studied its expression at different stages of tumor development using the mouse skin carcinogenesis model. VEGF/VPF mRNA was induced in skin in vivo after 12-O-tetradecanoylphorbol-13-acetate treatment. Constitutive up-regulation of VEGF/VPF at the mRNA and protein levels was also observed in premalignant papillomas and, at a higher level, in squamous carcinomas, suggesting a correlation between VEGF/VPF expression and tumor progression. A direct positive correlation between VEGF/VPF mRNA expression and the level of activated H-ras gene was found in a series of cell lines representing different stages of epidermal tumor development. Consequently, a clone of one of these cell lines, HaCa4, which has lost most of its v-ras expression, down-regulated VEGF mRNA expression concomitantly with its metastatic potential. Direct evidence of H-ras involvement in VEGF induction was obtained when an immortalized mouse keratinocyte cell line transduced with a retrovirus carrying v-H-ras showed highly increased VEGF/VPF mRNA levels. These data show that in mouse skin carcinogenesis, the VEGF/VPF angiogenic stimulus occurs early during premalignant papilloma development and further increases at later stages. Moreover, we demonstrate that increasing the activated H-ras dose, a phenomenon that takes place sequentially throughout mouse skin tumor development, may play an additional role by facilitating malignant in vivo progression through the modulation of VEGF/VPF-mediated angiogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carcinoma, Squamous Cell / chemically induced
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / pathology
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic / genetics*
  • Disease Progression
  • Endothelial Growth Factors / biosynthesis*
  • Endothelial Growth Factors / genetics
  • Endothelial Growth Factors / physiology
  • Female
  • Gene Expression Regulation*
  • Gene Expression Regulation, Neoplastic
  • Genes, ras*
  • Interleukin 1 Receptor Antagonist Protein
  • Keratinocytes / drug effects
  • Lymphokines / biosynthesis*
  • Lymphokines / genetics
  • Lymphokines / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Mice, Inbred SENCAR
  • Neoplasm Metastasis
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics
  • Neovascularization, Pathologic / genetics*
  • Neovascularization, Pathologic / physiopathology
  • Oncogene Protein p21(ras) / physiology
  • Papilloma / chemically induced
  • Papilloma / genetics*
  • Papilloma / pathology
  • Precancerous Conditions / genetics
  • Precancerous Conditions / pathology
  • Proto-Oncogene Proteins p21(ras) / physiology
  • RNA, Messenger / biosynthesis
  • RNA, Neoplasm / biosynthesis
  • Sialoglycoproteins / biosynthesis
  • Sialoglycoproteins / genetics
  • Skin Neoplasms / chemically induced
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology
  • Species Specificity
  • Tetradecanoylphorbol Acetate
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • Endothelial Growth Factors
  • Il1rn protein, mouse
  • Interleukin 1 Receptor Antagonist Protein
  • Lymphokines
  • Neoplasm Proteins
  • RNA, Messenger
  • RNA, Neoplasm
  • Sialoglycoproteins
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Oncogene Protein p21(ras)
  • Proto-Oncogene Proteins p21(ras)
  • Tetradecanoylphorbol Acetate