Nonlinkage of 16q markers to familial predisposition to Wilms' tumor

Cancer Res. 1992 Nov 1;52(21):6117-20.

Abstract

Wilms' tumor (WT), a childhood cancer of the kidney, occurs in both familial and sporadic forms. Chromosome 11 genes have been implicated in the etiology of WT, and mutations in a gene at chromosomal band 11p13, WT1, have been identified in a few WT cases. However, 11p13 has been excluded as the site of the predisposition mutation segregating in several large WT families, which implies the existence of a non-11p familial predisposition gene. Recently, loss of heterozygosity for 16q markers located between chromosomal bands 16q13 and 16q22 has been reported in approximately 20% of sporadic Wilms' tumors. To determine if this region of 16q harbors the non-11p familial WT gene, a genetic linkage study of five WT families was undertaken. Using multipoint analyses, we ruled out genetic linkage of familial WT predisposition to 16q.

Publication types

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

MeSH terms

  • Chromosome Banding
  • Chromosomes, Human, Pair 16*
  • Female
  • Genes, Wilms Tumor*
  • Genetic Markers
  • Humans
  • Kidney Neoplasms / genetics*
  • Lod Score*
  • Male
  • Pedigree
  • Polymorphism, Restriction Fragment Length
  • Wilms Tumor / genetics*

Substances

  • Genetic Markers