Analysis of WT1 in granulosa cell and other sex cord-stromal tumors

Cancer Res. 1993 Jun 15;53(12):2712-4.

Abstract

The molecular genetic events involved in the etiology of granulosa cell, Sertoli cell, and Leydig cell tumors are unknown. The expression of the Wilms' tumor suppressor gene WT1 in granulosa and Sertoli cells prompted us to analyze this gene for mutations in 11 granulosa cell tumors, three Leydig cell tumors, and one Sertoli/Leydig cell tumor. Although most of these tumors express WT1 mRNA, none harbors a WT1 mutation in the zinc finger domains where > 90% of WT1 mutations in sporadic Wilms' tumors have been found. In addition we were able to exclude tumor-specific loss of heterozygosity in 13 of 15 cases. Taken together these results suggest that the WT1 gene is unlikely to play an important role in the development of sex cord-stromal tumors.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Base Sequence
  • Child
  • Chromosomes, Human, Pair 11*
  • DNA, Neoplasm / chemistry*
  • DNA, Neoplasm / genetics
  • Exons / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic / genetics*
  • Granulosa Cell Tumor / genetics*
  • Humans
  • Leydig Cell Tumor / genetics*
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Ovarian Neoplasms / genetics*
  • Sertoli Cell Tumor / genetics*
  • Testicular Neoplasms / genetics*

Substances

  • DNA, Neoplasm