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Unique Bisphenol A Transcriptome in Prostate Cancer: Novel Effects on ERβ Expression That Correspond to Androgen Receptor Mutation Status
Author(s) -
Janet K. Hess-Wilson,
Siobhan Webb,
Hannah K. Daly,
YuetKin Leung,
Joanne Boldison,
Clay E.S. Comstock,
Maureen A. Sartor,
ShukMei Ho,
Karen E. Knudsen
Publication year - 2007
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.10283
Subject(s) - prostate cancer , androgen receptor , cancer research , transcriptome , biology , estrogen receptor , mutation , germline mutation , cancer , endocrinology , medicine , microbiology and biotechnology , gene expression , genetics , gene , breast cancer
Prostatic adenocarcinomas are dependent on androgen receptor (AR) activity for growth and progression, and therapy for disseminated disease depends on ablation of AR activity. Recurrent tumors ultimately arise wherein AR has been re-activated. One mechanism of AR restoration is via somatic mutation, wherein cells containing mutant receptors become susceptible to activation by alternative ligands, including bisphenol A (BPA). In tumors with specific AR mutations, BPA promotes therapeutic bypass, suggesting significant negative impact to the clinical management of prostate cancer.

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