Chemopreventive Agents Attenuate Rapid Inhibition of Gap Junctional Intercellular Communication Induced by Environmental Toxicants

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Publikace nespadá pod Filozofickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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BABICA Pavel ČTVERÁČKOVÁ Lucie LENČEŠOVÁ Zuzana TROSKO James E. UPHAM Brad L.

Rok publikování 2016
Druh Článek v odborném periodiku
Časopis / Zdroj Nutrition and cancer : an international journal
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www http://www.tandfonline.com/doi/abs/10.1080/01635581.2016.1180409?journalCode=hnuc20
Doi http://dx.doi.org/10.1080/01635581.2016.1180409
Obor Onkologie a hematologie
Klíčová slova CELL-CELL COMMUNICATION; CANCER CHEMOPREVENTION; STEM-CELLS; GREEN TEA; H2O2-INDUCED INHIBITION; CHEMICAL CARCINOGENESIS; DOWN-REGULATION; CHEMOTHERAPY; PREVENTION; QUERCETIN
Popis Altered gap junctional intercellular communication (GJIC) has been associated with chemical carcinogenesis, where both chemical tumor promoters and chemopreventive agents (CPAs) are known to conversely modulate GJIC. The aim of this study was to investigate whether attenuation of chemically inhibited GJIC represents a common outcome induced by different CPAs, which could be effectively evaluated using in vitro methods. Rat liver epithelial cells WB-F344 were pretreated with a CPA for either 30min or 24h, and then exposed to GJIC-inhibiting concentration of a selected tumor promoter or environmental toxicant [12-O-tetradecanoylphorbol-13-acetate (TPA), lindane, fluoranthene, 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (DDT), perfluorooctanoic acid (PFOA), or pentachlorophenol]. Out of nine CPAs tested, quercetin and silibinin elicited the most pronounced effects, preventing the dysregulation of GJIC by all the GJIC inhibitors, but DDT. Metformin and curcumin attenuated the effects of three GJIC inhibitors, whereas the other CPAs prevented the effects of two (diallyl sulfide, emodin) or one (indole-3-carbinol, thymoquinone) GJIC inhibitor. Significant attenuation of chemically induced inhibition of GJIC was observed in 27 (50%) out of 54 possible combinations of nine CPAs and six GJIC inhibitors. Our data demonstrate that in vitro evaluation of GJIC can be used as an effective screening tool for identification of chemicals with potential chemopreventive activity.
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