Inhibitory modulation of human estrogen receptor α and β activities by dicyclohexyl phthalate in human breast cancer cell lines
Author:
Affiliation:
1. Department of Molecular Biology, Daiichi University of Pharmacy
2. Laboratory of Xenobiotic Metabolism and Environmental Toxicology, Faculty of Pharmaceutical Sciences, Hiroshima International University (HIU)
Publisher
Japanese Society of Toxicology
Subject
Toxicology
Link
https://www.jstage.jst.go.jp/article/jts/42/4/42_417/_pdf
Reference20 articles.
1. CERI (Chemicals Evaluation and Research Institute, Japan) (2001): 2000 Contract investigation/research on environment-compatible technology development on behalf of the Ministry of Environment and Industry – Report on evaluation and method development for hormone-like effects of exogenous substances.
2. Forsell, C., Enmark, E., Axelman, K., Blomberg, M., Wahlund, L.O., Gustafsson, J.A. and Lannfelt, L. (2001): Investigations of a CA repeat in the oestrogen receptor β gene in patients with Alzheimer’s disease. Eur. J. Hum. Genet., 9, 802-804.
3. Harris, C.A., Henttu, P., Parker, M.G. and Sumpter, J.P. (1997): The estrogenic activity of phthalate esters in vitro. Environ. Health Perspect., 105, 802-811.
4. Honma, N., Horii, R., Iwase, T., Saji, S., Younes, M., Takubo, K., Matsuura, M., Ito, Y., Akiyama, F. and Sakamoto, G. (2008): Clinical importance of estrogen receptor-β evaluation in breast cancer patients treated with adjuvant tamoxifen therapy. J. Clin. Oncol., 26, 3727-3734.
5. Holliday, D.L. and Speirs, V. (2011): Choosing the right cell line for breast cancer research. Breast Cancer Res., 13, 215.
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