[Molecular genetic mechanism of the kidney cancer]

Nihon Rinsho. 2001 Jan;59(1):104-9.
[Article in Japanese]

Abstract

The oncogenic mechanisms of renal cell carcinoma(RCC) are becoming elucidated with recent advances in molecular biology. von Hipple-Lindau disease(VHL) tumor suppressor gene is mutated and inactivated frequently in clear cell type RCCs. The VHL protein forms a complex which shows a ubiquitin ligase activity. The lost of the ubiquitin ligase activity of VHL protein may be a key step for clear cell tumorigenesis. Papillary renal cell carcinomas are caused by activating mutation in the tyrosine kinase domain of the MET gene. This tumorigenic pathway is regulated by c-Src. Immunogene therapies have been started for the patients with advanced RCC. The information based on microarray and Serial Analysis of Gene Expression(SAGE) will provide novel diagnosis and therapy which focus on the tumorigenic mechanism of RCC in the near future.

Publication types

  • Review

MeSH terms

  • Animals
  • Carcinoma, Renal Cell / genetics*
  • Carcinoma, Renal Cell / therapy
  • Gene Expression Profiling
  • Genes, Suppressor / genetics
  • Genes, src
  • Genetic Therapy
  • Humans
  • Kidney Neoplasms / genetics*
  • Kidney Neoplasms / therapy
  • Ligases*
  • Mutation
  • Protein-Tyrosine Kinases / genetics
  • Proteins / genetics
  • Proto-Oncogene Proteins c-met / genetics
  • Tumor Suppressor Proteins*
  • Ubiquitin-Protein Ligases*
  • Von Hippel-Lindau Tumor Suppressor Protein
  • von Hippel-Lindau Disease / genetics

Substances

  • Proteins
  • Tumor Suppressor Proteins
  • Ubiquitin-Protein Ligases
  • Von Hippel-Lindau Tumor Suppressor Protein
  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-met
  • Ligases
  • VHL protein, human