Loss of heterozygosity at 7q22 and mutation analysis of the CDP gene in human epithelial ovarian tumors

Int J Cancer. 2001 Feb 1;91(3):345-9. doi: 10.1002/1097-0215(200002)9999:9999<::aid-ijc1050>3.0.co;2-1.

Abstract

Many tumor types including that of the ovary show loss of heterozygosity (LOH) on chromosome arm 7q, which suggests the existence of at least one tumor suppressor gene (TSG) on this chromosome arm. We have studied the region surrounding the putative tumor suppressor gene CUTL1 at 7q22 in 127 epithelial ovarian tumors. LOH was found across 7q22 in 31% of malignant and 14% of benign ovarian tumors. In 16% of the tumors the LOH appeared to be centered on the CUTL1 gene. This gene has been implicated previously as a TSG in both uterine leiomyomas and breast carcinoma. However, mutation analysis of the CUTL1 gene in 47 tumors with 7q22 LOH failed to identify any somatic alterations in the coding regions. This finding suggests that CUTL1 may not be the target of the 7q22 LOH in ovarian cancers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma, Mucinous / genetics
  • Carcinoma, Endometrioid / genetics
  • Chromosomes, Human, Pair 7 / genetics*
  • Cystadenocarcinoma, Serous / genetics
  • DNA Mutational Analysis
  • DNA Primers / genetics
  • Female
  • Genes, Tumor Suppressor / genetics*
  • Homeodomain Proteins
  • Humans
  • Loss of Heterozygosity*
  • Microsatellite Repeats / genetics
  • Neoplasm Proteins / genetics*
  • Nuclear Proteins / genetics*
  • Ovarian Neoplasms / genetics*
  • Repressor Proteins / genetics*
  • Transcription Factors

Substances

  • CUX1 protein, human
  • DNA Primers
  • Homeodomain Proteins
  • Neoplasm Proteins
  • Nuclear Proteins
  • Repressor Proteins
  • Transcription Factors