Disruption of Gap Junctions in Toxicity and Carcinogenicity
Author(s) -
James Kevin Chipman,
Angela Mally,
Gareth O. Edwards
Publication year - 2003
Publication title -
toxicological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.352
H-Index - 183
eISSN - 1096-6080
pISSN - 1096-0929
DOI - 10.1093/toxsci/71.2.146
Subject(s) - connexin , bystander effect , gap junction , downregulation and upregulation , toxicity , carcinogen , cancer research , mechanism of action , biology , homeostasis , cancer , microbiology and biotechnology , intracellular , toxicology , bioinformatics , medicine , immunology , genetics , in vitro , gene
Although the specific role of connexin-mediated gap junctional intercellular communication in the control of cell homeostasis, proliferation, and death are still not clear, several lines of evidence support these roles. The disturbance of this communication, through multiple mechanisms, may in the short term be a protective mechanism to limit the spread of toxicity in a tissue following chemical or radiation damage. However, sustained downregulation confers a loss of tumor-suppressive action. Consequently, connexin dysfunction has been associated with both the action of many carcinogens and being a feature of cancer per se. Connexins offer not only a target for cancer chemoprevention but also for exploitation in chemotherapy through the "bystander" effect.
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