Antiproliferative and apoptotic effects of selective phenolic acids on T47D human breast cancer cells: potential mechanisms of action

[1] Bonnesen C(2001)Dietary indoles and isothiocyanates that are generated from cruciferous vegetables can both stimulate apoptosis and confer protection against DNA damage in human colon cell lines Cancer Res 61 6120-6130

[2] Eggleston IM(1998)PD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase Mol Pharmacol 53 438-445

[3] Hayes JD(1999)Suppression of cell cycle progression by flavonoids: dependence on the aryl hydrocarbon receptor Carcinogenesis 20 1561-1566

[4] Reiners JJ(1997)Mechanism of inhibition of MDA-MB-468 breast cancer cell growth by 2,3,7,8-tetrachlorodibenzo-p-dioxin Carcinogenesis 18 925-933

[5] Lee JY(1994)Antiestrogenic effect of 2,3,7,8-tetrachlorodibenzo- Cancer Res 54 2707-2713

[6] Clift RE(2000)-dioxin on 17 beta-estradiol-induced pS2 expression Int J Cancer 88 902-906

[7] Dudley DT(1998)Increased expression of cytochrome p450 1A1 and 1B1 genes in anti-estrogen-resistant human breast cancer cell lines Cancer Res 58 5707-5712

[8] Myrand SP(1999)Resveratrol inhibits transcription of CYP1A1 in vitro by preventing activation of the aryl hydrocarbon receptor Br J Cancer 79 1340-1346

[9] Reiners JJ(1993)The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor Biochem Pharmacol 45 1129-1136

[10] Clift R(2002)Ah receptor binding properties of indole carbinols and induction of hepatic estradiol hydroxylation J Biol Chem 277 24780-24787

[1] Bonnesen C(2001)Dietary indoles and isothiocyanates that are generated from cruciferous vegetables can both stimulate apoptosis and confer protection against DNA damage in human colon cell lines Cancer Res 61 6120-6130

[2] Eggleston IM(1998)PD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase Mol Pharmacol 53 438-445

[3] Hayes JD(1999)Suppression of cell cycle progression by flavonoids: dependence on the aryl hydrocarbon receptor Carcinogenesis 20 1561-1566

[4] Reiners JJ(1997)Mechanism of inhibition of MDA-MB-468 breast cancer cell growth by 2,3,7,8-tetrachlorodibenzo-p-dioxin Carcinogenesis 18 925-933

[5] Lee JY(1994)Antiestrogenic effect of 2,3,7,8-tetrachlorodibenzo- Cancer Res 54 2707-2713

[6] Clift RE(2000)-dioxin on 17 beta-estradiol-induced pS2 expression Int J Cancer 88 902-906

[7] Dudley DT(1998)Increased expression of cytochrome p450 1A1 and 1B1 genes in anti-estrogen-resistant human breast cancer cell lines Cancer Res 58 5707-5712

[8] Myrand SP(1999)Resveratrol inhibits transcription of CYP1A1 in vitro by preventing activation of the aryl hydrocarbon receptor Br J Cancer 79 1340-1346

[9] Reiners JJ(1993)The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor Biochem Pharmacol 45 1129-1136

[10] Clift R(2002)Ah receptor binding properties of indole carbinols and induction of hepatic estradiol hydroxylation J Biol Chem 277 24780-24787