Turcot's Syndrome of Glioma and Polyposis Occurs in the Absence of Germ Line Mutations of Exons 5 to 9 of the p53 Gene

Academic Article

Abstract

  • The term “Turcot's syndrome” has been used to describe approxima-tively 55 patients with an association of colonic polyposis and primary neuroepithelial tumors of the central nervous system. The pS3 tumor suppressor gene is a possible candidate underlying the syndrome because (a) mutations in the p53 gene are ubiquitous in human cancer, including colon carcinoma and gliomas, and (b) somatic or germ line mutations of the p53 tumor suppressor gene cause the Li-Fraumeni syndrome, which is characterized by the association of breast and soft tissue tumors. We determined the DNA sequence of the conserved regions of the p53 gene (exons 5 to 9) in the tumor tissues and lymphocytes of two patients with glioma-polyposis and found that mutations did occur as independent tumor-specific alterations but did not involve the germ line of these patients, suggesting that p53 may play a role in progression but not initiation of the disease. © 1993, American Association for Cancer Research. All rights reserved.
  • Authors

    Published In

  • Cancer Research  Journal
  • Author List

  • Kikuchi T; Rempel SA; Rutz HP; Tribolet ND; Mulligan L; Cavenee WK; Jothy S; Leduy L; Van Meir EG
  • Start Page

  • 957
  • End Page

  • 961
  • Volume

  • 53
  • Issue

  • 5