Enhancement of gap junctional communication by retinoids correlates with their ability to inhibit neoplastic transformation

Mohammad Z. Hossain, Lynne R. Wilkens, Parmender P. Mehta, Werner Loewenstein, John S. Bertram

Research output: Contribution to journalArticle

140 Scopus citations

Abstract

Retinoids that cause inhibition of methylcbolanthrene-induced neoplastic transformation of C3H/10T1/2 cells enhance gap-junctional communication in carcinogen-initiated cells. Dose-response studies using retinoids of diverse structures and potency demonstrated a good correlation between these two events. Junctional permeability was enhanced by retinol and tetrahydrotetramethylnaphthalenyl propenylbenzok acid (TTNPB) at concentrations from 10-8 to 10-6 M, and by retinoic acid between 10-8 and 10-6 M, the same concentrations that inhibited neoplastic transformation. Retinoic acid inhibited permeability at 10-10 M, at which concentration transformation was enhanced. Retinoids caused similar alterations in communication in parental 10T1/2 cells. Communication between initiated and 10T1/2 cells was not influenced by TTNPB. The tumor promoter 12-O-tetrade-canoylphorbol-13-acetate (TPA) inhibited junctional communication in initiated cells, in 10T1/2 cells and between these two cell lines. After repeated exposure of 10T1/2 cells to TPA only retinoid-enhanced communication was blocked; in contrast, basal communication became refractory. It is proposed that much of the chemopreventive action of retinoids can be explained by the enhanced junctional communication of growth regulatory signals.

Original languageEnglish (US)
Pages (from-to)1743-1748
Number of pages6
JournalCarcinogenesis
Volume10
Issue number9
DOIs
Publication statusPublished - Sep 1 1989

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ASJC Scopus subject areas

  • Cancer Research

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