BABICA, Pavel, Lucie ČTVERÁČKOVÁ, Zuzana LENČEŠOVÁ, James E. TROSKO and Brad L. UPHAM. Chemopreventive Agents Attenuate Rapid Inhibition of Gap Junctional Intercellular Communication Induced by Environmental Toxicants. Nutrition and cancer : an international journal. ABINGDON: ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD, 2016, vol. 68, No 5, p. 827-837. ISSN 0163-5581. Available from: https://dx.doi.org/10.1080/01635581.2016.1180409.
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Basic information
Original name Chemopreventive Agents Attenuate Rapid Inhibition of Gap Junctional Intercellular Communication Induced by Environmental Toxicants
Authors BABICA, Pavel (203 Czech Republic, guarantor, belonging to the institution), Lucie ČTVERÁČKOVÁ (203 Czech Republic, belonging to the institution), Zuzana LENČEŠOVÁ (203 Czech Republic, belonging to the institution), James E. TROSKO (840 United States of America) and Brad L. UPHAM (840 United States of America).
Edition Nutrition and cancer : an international journal, ABINGDON, ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD, 2016, 0163-5581.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.447
RIV identification code RIV/00216224:14310/16:00093527
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1080/01635581.2016.1180409
UT WoS 000380883200013
Keywords in English CELL-CELL COMMUNICATION; CANCER CHEMOPREVENTION; STEM-CELLS; GREEN TEA; H2O2-INDUCED INHIBITION; CHEMICAL CARCINOGENESIS; DOWN-REGULATION; CHEMOTHERAPY; PREVENTION; QUERCETIN
Tags AKR, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Michaela Hylsová, Ph.D., učo 211937. Changed: 2/3/2017 12:12.
Abstract
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.
Links
LM2015051, research and development projectName: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX RI)
Investor: Ministry of Education, Youth and Sports of the CR
LO1214, research and development projectName: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX)
Investor: Ministry of Education, Youth and Sports of the CR
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