The effect of several tumor promoters (12-O-tetradecanoyl-phorbol-13-acetate (TPA); 1,1′-(2,2,2-trichloroethylidene)bis[4-chlorobenzene] (DDT); Aroclor1260, and clofibrate) on the inhibition of gap junctional intercellular communication (GJIC) and intracellular calcium concentration ([Ca2 ]i) was studied in a cell line consisting of initiated cells (3PC). In addition, the effect of different extracellular calcium concentrations ([Ca2 ]e) on the effects of tumor promoters on both GJIC and [Ca2 ]i were studied. Agents with GJIC inhibiting capacity increased [Ca2 ]i. However, the increase of [Ca2 ]i did not (always) precede GJIC inhibition. The effect of tumor promoters on GJIC were similar under low (0.05 mM) and high (1.20 mM) Ca2 e conditions, while different effects on [Ca2 ]i were found. These results suggest that tumor promoters can inhibit GJIC and change [Ca2 ]i, but that there is no direct relationship between these two processes.
Jansen, L. A. M., de Vrije, T., Koeman, J. H., & Jongen, W. M. F. (1997). The role of calcium in the tumor promoter-induced inhibition of gap junctional intercellular communication. Environmental Toxicology and Pharmacology, 3, 13-16. https://doi.org/10.1016/S1382-6689(96)00132-9