J 2019

n-3 Polyunsaturated fatty acids alter benzo[a]pyrene metabolism and genotoxicity in human colon epithelial cell models

TYLICHOVÁ, Zuzana; Jiri NECA; Jan TOPINKA; Alena MILCOVA; Jiřina HOFMANOVÁ et. al.

Základní údaje

Originální název

n-3 Polyunsaturated fatty acids alter benzo[a]pyrene metabolism and genotoxicity in human colon epithelial cell models

Autoři

TYLICHOVÁ, Zuzana (203 Česká republika, domácí); Jiri NECA; Jan TOPINKA; Alena MILCOVA; Jiřina HOFMANOVÁ (203 Česká republika, domácí); Alois KOZUBÍK (203 Česká republika, domácí); Miroslav MACHALA (203 Česká republika) a Jan VONDRÁČEK (203 Česká republika, garant)

Vydání

Food and Chemical Toxicology, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2019, 0278-6915

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30304 Public and environmental health

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 4.679

Kód RIV

RIV/00216224:14310/19:00113499

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000458712400031

EID Scopus

2-s2.0-85058936647

Klíčová slova anglicky

Colon cancer; Eicosapentaenoic acid; Docosahexaenoic acid; Polycyclic aromatic hydrocarbon; DNA damage

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 16. 4. 2020 14:51, Mgr. Michal Petr

Anotace

V originále

Dietary carcinogens, such as benzo[a]pyrene (BaP), are suspected to contribute to colorectal cancer development. n-3 Polyunsaturated fatty acids (PUFAs) decrease colorectal cancer risk in individuals consuming diets rich in PUFAs. Here, we investigated the impact of eicosapentaenoic (EPA) and docosahexaenoic (DHA) acid on metabolism and genotoxicity of BaP in human cell models derived from the colon: HT-29 and HCT-116 cell lines. Both PUFAs reduced levels of excreted BaP metabolites, in particular BaP-tetrols and hydroxylated BaP metabolites, as well as formation of DNA adducts in HT-29 and HCT-116 cells. However, EPA appeared to be a more potent inhibitor of formation of some intracellular BaP metabolites, including BaP-7,8-dihydrodiol. EPA also reduced phosphorylation of histone H2AX (Ser139) in HT-29 cells, which indicated that it may reduce further forms of DNA damage, including DNA double strand breaks. Both PUFAs inhibited induction of CYP1 activity in colon cells determined as 7-ethoxyresorufin-O-deethylase (EROD); this was at least partly linked with inhibition of induction of CYP1A1, 1A2 and 1B1 mRNAs. The downregulation and/or inhibition of CYP1 enzymes by PUFAs could thus alter metabolism and reduce genotoxicity of BaP in human colon cells, which might contribute to known chemopreventive effects of PUFAs in colon epithelium.