Recent advances in Wilms tumor genetics

Curr Opin Pediatr. 2002 Feb;14(1):5-11. doi: 10.1097/00008480-200202000-00002.

Abstract

The past decade has witnessed substantial growth in our knowledge of the genes and loci that are altered in Wilms tumor. Although Wilms tumor was one of the original paradigms of Knudson's two-hit model of cancer formation, it has become apparent that several genetic events contribute to Wilms tumorigenesis. Recent research has identified targets and regulators of the first Wilms tumor gene, WT1, has uncovered several candidate genes at the second Wilms tumor locus, WT2, and has identified two familial Wilms tumor loci, FWT1 and FWT2. The recent discovery of activating beta-catenin mutations in some Wilms tumors has also implicated the Wnt signaling pathway in this neoplasm. Recurrent abnormalities of other loci, including 16q, 1p, and 7p, have indicated that these sites may harbor Wilms tumor genes. An enhanced understanding of these and other genetic lesions will provide the foundation for novel targeted Wilms tumor therapies.

Publication types

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

MeSH terms

  • Beckwith-Wiedemann Syndrome / genetics
  • Child
  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 16
  • Chromosomes, Human, Pair 7
  • Cytoskeletal Proteins
  • Genes, Wilms Tumor*
  • Genes, p53
  • Humans
  • Kidney Neoplasms / genetics*
  • Trans-Activators*
  • WAGR Syndrome / genetics
  • Wilms Tumor* / genetics*
  • beta Catenin

Substances

  • CTNNB1 protein, human
  • Cytoskeletal Proteins
  • Trans-Activators
  • beta Catenin