[1] |
Nguyen LP, Bradfield CA. The search for endogenous activators of the aryl hydrocarbon receptor. Chem Res Toxicol, 2008; 21, 102-16. doi: 10.1021/tx7001965 |
[2] |
Quattrochi LC, Vu T, Tukey RH. The human CYP1A2 gene and induction by 3-methylcholanthrene. A region of DNA that supports AH-receptor binding and promoter-specific induction. J Biol Chem, 1994; 269, 6949-54. http://www.jbc.org/content/269/9/6949.full.pdf |
[3] |
Willett KL, Wassenberg D, Lienesch L, et al, In vivo and in vitro inhibition of CYP1A-dependent activity in Fundulus heteroclitus by the polynuclear aromatic hydrocarbon fluoranthene. Toxicol Appl Pharmacol, 2001; 177, 264-71. doi: 10.1006/taap.2001.9296 |
[4] |
Perepechaeva ML, YA Sidorova, AY Grishanova. Weak CYP1A Inducers: A Potential Role in Prevention and Therapy of Chemically-Induced Cancer. Cancer Etiology, Diagnosis and Treatments. 2013, New York: Nova Science Publishers, Inc. |
[5] |
G Sharmila, FA Bhat, R Arunkuma, et al. Chemopreventive effect of quercetin, a natural dietary flavonoid on prostate cancer in in vivo model. Clin Nutr, 2013; 33, 718-26. https://www.researchgate.net/profile/Elumalai_Perumal/publication/259250552_Chemopreventive_Effect_of_Quercetin_in_MNU_and_Testosterone_Induced_Prostate_Cancer_of_Sprague-Dawley_Rats/links/53e090110cf2aede4b4cd166.pdf?origin=publication_detail |
[6] |
Chen Y, Xiao P, Ou-Yang DS, et al. Simultaneous action of the flavonoid quercetin on cytochrome P450 (CYP) 1A2, CYP2A6, N-acetyltransferase and xanthine oxidase activity in healthy volunteers. Clin Exp Pharmacol Physiol, 2009; 36, 828-33. doi: 10.1111/cep.2009.36.issue-8 |
[7] |
Oesch-Bartlomowicz B, F Oesch. Phosphorylation of xenobiotic-metabolizing cytochromes P450. Anal Bioanal Chem, 2008; 392, 1085-92. doi: 10.1007/s00216-008-2315-2 |
[8] |
Zhang S, Qin C, Safe SH. Flavonoids as aryl hydrocarbon receptor agonists/antagonists: effects of structure and cell context. Environ Health Perspect, 2003; 111, 1877-82. doi: 10.1289/ehp.6322 |
[9] |
Niestroy J, Barbara A, Herbst K, et al. Single and concerted effects of benzo[a]pyrene and flavonoids on the AhR and Nrf2-pathway in the human colon carcinoma cell line Caco-2. Toxicol In Vitro, 2011; 25, 671-83. doi: 10.1016/j.tiv.2011.01.008 |
[10] |
Mohammadi-Bardbori A, Bengtsson J, Rannug U, et al. Quercetin, resveratrol, and curcumin are indirect activators of the aryl hydrocarbon receptor (AHR). Chem Res Toxicol, 2012; 25, 1878-84. doi: 10.1021/tx300169e |