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Cited by 267

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From estrogen to androgen receptor: A new pathway for sex hormones in prostate

Open access
Yeh, Shuyuan, Miyamoto, Hiroshi, Shima, Hiroki, Chang, Chawnshang·1998·Proceedings of the National Academy of Sciences

Abstract

While all three coactivators ARA 70 , steroid receptor coactivator 1, and RAC3/ACTR can enhance androgen receptor (AR) transcriptional activity at 1 nM dihydrotestosterone, we here demonstrate that only ARA 70 can induce AR transcriptional activity >30-fold in the presence of 10 nM 17β-estradiol (E2), but not diethylstilbestrol. The significance of this newly described E2-induced AR transcriptional activity in DU145 human prostate cancer cells was further strengthened by finding patients with Reifenstein partial-androgen-insensitive syndrome that fail in the E2-AR-ARA 70 pathway. Together, our data suggest, for the first time, testosterone/dihydrotestosterone may not be the only ligands for the AR. E2 represents another important natural ligand for AR that may play an essential role for the AR function and the development of the male reproductive system.

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Metadata

Authors
Yeh, S., Miyamoto, H., Shima, H., & Chang, C.
Venue
Proceedings of the National Academy of Sciences
Published
1998-05-12
Volume
95
Issue
10
Pages
5527-5532
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2137676273
Cited by
267
References
1
FWCI
25.13
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: From estrogen to androgen receptor: A new pathway for sex hormones in prostate. https://app.cochat.ai/papers/10.1073/pnas.95.10.5527
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Yeh, S., Miyamoto, H., Shima, H., & Chang, C. (1998). From estrogen to androgen receptor: A new pathway for sex hormones in prostate. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.95.10.5527

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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