D. C. Spink, H. P. Eugster, D. W. Lincoln 2nd, J. D. Schuetz, E. G. Schuetz, J. A. Johnson, et al., “17 Beta-Estradiol Hydroxylation Catalyzed by Human Cytochrome P450 1A1 A Comparison of the Activities Induced by 2,3,7,8-Tetrachlorodibenzo-p-Dioxin in MCF-7 Cells with Those from Heterologous Expression of the cDNA,” Archives of Biochemistry and Biophysics, Vol. 293, No. 2, 1992, pp. 342-348. doi10.1016/0003-9861(92)90404-K - References

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D. C. Spink, H. P. Eugster, D. W. Lincoln 2nd, J. D. Schuetz, E. G. Schuetz, J. A. Johnson, et al., “17 Beta-Estradiol Hydroxylation Catalyzed by Human Cytochrome P450 1A1: A Comparison of the Activities Induced by 2,3,7,8-Tetrachlorodibenzo-p-Dioxin in MCF-7 Cells with Those from Heterologous Expression of the cDNA,” Archives of Biochemistry and Biophysics, Vol. 293, No. 2, 1992, pp. 342-348. doi:10.1016/0003-9861(92)90404-K

has been cited by the following article:

TITLE: The Aryl Hydrocarbon Receptor: A Target for Breast Cancer Therapy

AUTHORS: Joann B. Powell, Gennifer D. Goode, Sakina E. Eltom

KEYWORDS: Aryl Hydrocarbon Receptor; Therapeutic Targeting; Breast Cancer Progression; Chemosensitization

JOURNAL NAME: Journal of Cancer Therapy, Vol.4 No.7, August 22, 2013

ABSTRACT: The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that regulates a battery of genes in response to exposure to a broad class of environmental poly aromatic hydrocarbons (PAH). AhR is historically characterized for its role in mediating the toxicity and adaptive responses to these chemicals, however mounting evidence has established a role for it in ligand-independent physiological processes and pathological conditions, including cancer. The AhR is overexpressed and constitutively activated in advanced breast cancer cases and was shown to drive the progression of breast cancer. In this article we will review the current state of knowledge on the possible role of AhR in breast cancer and how it will be exploited in targeting AhR for breast cancer therapy.

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