A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix

Cancer Res. 1998 Mar 15;58(6):1140-3.

Abstract

Adenoma malignum (AM) is known to be one of the malignant tumors that is commonly associated with Peutz-Jeghers syndrome. Recently, the genetic locus of Peutz-Jeghers syndrome was mapped to the telomeric region of chromosome 19p. We analyzed nine sporadic cases of AM with high-density loss of heterozygosity to study the region of chromosome 19p13.2-13.3 using eight microsatellite markers. Our deletion mapping data revealed a distinct region with 100% loss of heterozygosity frequency at marker D19S216. This result indicates that a putative tumor suppressor gene for AM is located at D19S216 on chromosomal band 19p13.3 and plays an important role in AM tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Adenoma / genetics*
  • Cell Separation
  • Chromosome Mapping
  • Chromosomes, Human, Pair 19*
  • Female
  • Genes, Tumor Suppressor*
  • Humans
  • Loss of Heterozygosity
  • Peutz-Jeghers Syndrome / genetics*
  • Sequence Deletion
  • Uterine Cervical Neoplasms / genetics*