Role of Mammalian Homologs of the Drosophila Discs Large 1 (dlg1) Gene in the Genesis of Epithelial Ovarian Cancer

Abstract

Mouse homologs of the Drosophila melanogaster tumor suppressor gene, discs large 1, have been examined for their presence in the ovarian surface epithelium (OSE), the origin of the most virulent and common form of ovarian cancer. The presence often such mouse genes was verified in the ovary by RT-PCR analysis of whole ovarian homogenates. Antibodies specific to each of the homologs were utilized to assess the presence of each protein in the surface epithelial layer. CASK and ZO-2 were both expressed in the surface epithelium as well as in other ovarian cell types. ZO-1 and SAP102 were not found in the surface epithelium although they were determined to be present in the granulosa cells. ZO-3 was not found in any of the ovarian tissues. Immunofluorescence could not positively localize five additional proteins, Dlgh1, Dlgh2, Dlgh3, p55, and PSD95 to any ovarian tissue; however, Dlgh2 and pSS proteins were found in whole ovarian lysates by western blot analysis. Primary cell cultures from mouse ovary surface epithelium have been established. The challenge, as yet unrealized, has been to target specifically the OSE expression of a protein. We propose a change in research objectives during the third year of funding to accomplish this objective.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2002
Accession Number
ADA411419

Entities

People

  • Carrie A. Stoltzman
  • Eli Y. Adashi
  • Gretchen J. King
  • Nikki J. Kirkman

Organizations

  • University of Utah

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Animals
  • Biology
  • Biomedical Research
  • Cancer
  • Cells
  • Culture Techniques
  • Diptera
  • Drosophila
  • Epithelial Cells
  • Fish
  • Genes
  • Neoplasms
  • Ovarian Cancer
  • Proteins
  • Synapses
  • Tissues

Fields of Study

  • Biology

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Molecular Genetics
  • Molecular and genetic basis of cancer.