Identification of Junctionally-Transmitted Growth Inhibitors

Abstract

We have proposed the identification of junctionally transmitted growth control signals which we hypothesize to be responsible for the growth inhibition of tumor cells when in junctional communication with normal cells. In order to test this hypothesis rigorously, we have genetically engineered human breast cancer cells to contain the gap junction gene connexin 43, under the control of a tetracycline inducible promoter. We have been successful in producing several clones in which connexin 43 is strongly induced on withdrawal of tetracycline and in which connexin 43 is integrated into the plasma membrane and is functional as determined by dye. injection studies. We have moreover shown that exposure of isolated cells to EGTA results in the opening of hemi--channels to the extra-cellular environment; expression of connexin 43 is required for this effect. To determine that any responses of cells are due to junctional transfer of signals, rather than the presence of a trans- membrane protein, we have similarly produced breast cancer cell lines containing a mutant connexin 43 gene in which the pore is predicted to be blocked. These molecular and biological tools put us in a good position to carefully address the stated hypothesis.

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 1999
Accession Number
ADA383351

Entities

People

  • John S. Bertram

Organizations

  • University of HawaiĘ»i System

Tags

DTIC Thesaurus Topics

  • Anti-Bacterial Agents
  • Antibodies
  • Breast Cancer
  • Cell Line
  • Cells
  • Identification
  • Inhibitors
  • Intercellular Junctions
  • Laboratory Animals
  • Materials
  • Membranes
  • Molecules
  • Neoplasms
  • Production
  • Proteins
  • Recombinant Dna
  • Tumor Cell Line

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics
  • Molecular Genetics

Technology Areas

  • Biotechnology