Simple numeric abnormalities as primary karyotype changes in ovarian carcinoma

Floyd H. Thompson, Yun Liu, Julia Emerson, Ronald Weinstein, Rosemary Makar, Jeffrey M. Trent, Raymond Taetle, David S. Alberts

Research output: Contribution to journalArticle

41 Scopus citations

Abstract

Simple near‐diploid karyotypes in ovarian cancer may indicate either primary alterations related to tumor pathogenesis or abnormalities associated with early tumor progression. We have identified a series of 13 epithelial ovarian tumors with very simple karyotypes. Specifically, these karyotypes were near‐diploid and displayed numeric abnormalities alone or combined with one or two structural alterations. The present series includes samples from 10 patients with newly diagnosed adenocarcinomas and 3 patients having borderline malignancies. Recurrent numeric abnormalities were identified and included 9/13 cases (69%) with + 12, eight cases (62%) with + 8, five cases (38%) with + 7, three cases (23%) each with + 3 or + 5, and two cases (15%) with ‐X, Five cases in this series displayed certain numeric abnormalities (+ 12, + 7, and ‐X) as the sole anomalies, thereby qualifying as primary karyotype changes. Of the 6 cases with structural abnormalities, 4 involved chromosome 19, 2 involved chromosome I, and the remaining abnormalities or translocation partners involved other chromosomes. These findings indicate that some numeric abnormalities are primary karyotype alterations in patients with malignant epithelial ovarian tumors and that chromosome 19 may be preferentially involved in structural rearrangements during early tumor progression. Genes Chromosom Cancer 10:262–266 (1994). © 1994 Wiley‐Liss, Inc.

Original languageEnglish (US)
Pages (from-to)262-266
Number of pages5
JournalGenes, Chromosomes and Cancer
Volume10
Issue number4
DOIs
StatePublished - Aug 1994

    Fingerprint

ASJC Scopus subject areas

  • Genetics
  • Cancer Research

Cite this