p53 accumulation in favorable-histology Wilms tumor is associated with angiogenesis and clinically aggressive disease

J Pediatr Surg. 2002 Mar;37(3):523-7. doi: 10.1053/jpsu.2002.30858.

Abstract

Background/purpose: Unfavorable histology (UH) in Wilms tumor has been linked to malfunction of the p53 tumor suppressor gene, which regulates (1) the endogenous angiogenesis suppressor thrombospondin-1 (TSP-1) and (2) vascular endothelial growth factor (VEGF). The authors hypothesized that clinically aggressive favorable histology Wilms tumor (FH), like UH, but distinct from standard-risk FH disease, would display altered p53/TSP-1 function and upregulated angiogenesis.

Methods: Three Wilms tumor specimens manifesting different histology and clinical behavior were obtained: clinically aggressive UH, clinically aggressive FH, and standard-risk FH disease. Xenografts were induced intrarenally in athymic mice. P53, TSP-1, and VEGF status and neovascularity were assessed in tumor tissues. Lungs were evaluated for metastasis.

Results: Clinically aggressive FH Wilms tumor displayed progressive alteration in p53/TSP-1 status and upregulation of VEGF. Such alteration was observed in the UH tumor, but was absent from the standard-risk FH tumor. Xenografts from clinically aggressive tumors displayed brisk neoangiogenesis and yielded lung metastases.

Conclusions: This is the first report of altered p53/TSP-1 function in association with clinically aggressive behavior in FH Wilms tumor. These characteristics were not observed in parallel studies of a nonaggressive FH tumor. Loss of wild-type p53 function may contribute to disease progression in FH Wilms tumor, in part by upregulation of VEGF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Endothelial Growth Factors / analysis
  • Endothelial Growth Factors / physiology
  • Humans
  • Immunohistochemistry
  • Kidney / surgery
  • Kidney Neoplasms / chemistry
  • Kidney Neoplasms / metabolism
  • Lung Neoplasms / chemistry
  • Lung Neoplasms / secondary
  • Lymphokines / analysis
  • Lymphokines / physiology
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Neoplasms, Experimental
  • Neovascularization, Pathologic / metabolism*
  • Neovascularization, Pathologic / pathology*
  • Paraffin Embedding
  • Platelet Endothelial Cell Adhesion Molecule-1 / analysis
  • Thrombospondin 1 / analysis
  • Thrombospondin 1 / physiology
  • Transplantation, Heterologous
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / analysis
  • Tumor Suppressor Protein p53 / metabolism*
  • Tumor Suppressor Protein p53 / physiology
  • Up-Regulation / physiology
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Wilms Tumor / blood supply*
  • Wilms Tumor / metabolism*
  • Wilms Tumor / pathology

Substances

  • Endothelial Growth Factors
  • Lymphokines
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Thrombospondin 1
  • Tumor Suppressor Protein p53
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors