Gene expression profiling in dorsolateral prostates of prepubertal and adult Sprague-Dawley rats dosed with estradiol benzoate, estradiol, and testosterone
Author:
Affiliation:
1. Division of Systems Biology, National Center for Toxicological Research, U.S. Food and Drug Administration, USA
Publisher
Japanese Society of Toxicology
Subject
Toxicology
Link
https://www.jstage.jst.go.jp/article/jts/45/8/45_435/_pdf
Reference51 articles.
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2. Bosland, M.C., Ford, H. and Horton, L. (1995): Induction at high incidence of ductal prostate adenocarcinomas in NBL/Cr and Sprague-Dawley Hsd:SD rats treated with a combination of testosterone and estradiol-17 beta or diethylstilbestrol. Carcinogenesis, 16, 1311-1317.
3. Bosland, M.C. (2005): The role of estrogens in prostate carcinogenesis: a rationale for chemoprevention. Rev. Urol., 7 (Suppl. 3), S4-S10.
4. Cheong, A., Zhang, X., Cheung, Y.Y., Tang, W.Y., Chen, J., Ye, S.H., Medvedovic, M., Leung, Y.K., Prins, G.S. and Ho, S.M. (2016): DNA methylome changes by estradiol benzoate and bisphenol A links early-life environmental exposures to prostate cancer risk. Epigenetics, 11, 674-689.
5. Diamanti-Kandarakis, E., Bourguignon, J.P., Giudice, L.C., Hauser, R., Prins, G.S., Soto, A.M., Zoeller, R.T. and Gore, A.C. (2009): Endocrine-disrupting chemicals: an Endocrine Society scientific statement. Endocr. Rev., 30, 293-342.
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