Characterization of flavonoids with potent and subtype-selective actions on estrogen receptors alpha and beta
Michael J. Bolt,
Jessica Oceguera,
Pankaj K. Singh,
Kazem Safari,
Derek H. Abbott,
Kaley A. Neugebauer,
Maureen G. Mancini,
Daniel A. Gorelick,
Fabio Stossi,
Michael A. Mancini
Affiliations
Michael J. Bolt
Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA; Center for Translational Cancer Research, Institute of Biosciences & Technology, Texas A&M University, Houston, TX 77030, USA
Jessica Oceguera
Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA; Center for Translational Cancer Research, Institute of Biosciences & Technology, Texas A&M University, Houston, TX 77030, USA
Pankaj K. Singh
Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA; Center for Translational Cancer Research, Institute of Biosciences & Technology, Texas A&M University, Houston, TX 77030, USA
Kazem Safari
Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA; Center for Translational Cancer Research, Institute of Biosciences & Technology, Texas A&M University, Houston, TX 77030, USA
Derek H. Abbott
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
Kaley A. Neugebauer
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center For Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA
Maureen G. Mancini
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
Daniel A. Gorelick
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center For Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA
Fabio Stossi
Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
Michael A. Mancini
Center for Advanced Microscopy and Image Informatics, Institute of Biosciences & Technology, Texas A&M University, and Baylor College of Medicine, Houston, TX 77030, USA; Center for Translational Cancer Research, Institute of Biosciences & Technology, Texas A&M University, Houston, TX 77030, USA; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX 77030, USA; Corresponding author
Summary: The initial step in estrogen-regulated transcription is the binding of a ligand to its cognate receptors, named estrogen receptors (ERα and ERβ). Phytochemicals present in foods and environment can compete with endogenous hormones to alter physiological responses. We screened 224 flavonoids in our engineered biosensor ERα and ERβ PRL-array cell lines to characterize their activity on several steps of the estrogen signaling pathway. We identified 83 and 96 flavonoids that can activate ERα or ERβ, respectively. While most act on both receptors, many appear to be subtype-selective, including potent flavonoids that activate ER at sub-micromolar concentrations. We employed an orthogonal assay using a transgenic zebrafish in vivo model that validated the estrogenic potential of these compounds. To our knowledge, this is the largest study thus far on flavonoids and the ER pathway, facilitating the identification of a new set of potential endocrine disruptors acting on both ERα and ERβ.