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Träfflista för sökning "WFRF:(Wu WF) srt2:(2015-2019)"

Search: WFRF:(Wu WF) > (2015-2019)

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  • Miao, YF, et al. (author)
  • An ERβ agonist induces browning of subcutaneous abdominal fat pad in obese female mice
  • 2016
  • In: Scientific reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 6, s. 38579-
  • Journal article (peer-reviewed)abstract
    • Estrogen, via estrogen receptor alpha (ERα), exerts several beneficial effects on metabolism and energy homeostasis by controlling size, enzymatic activity and hormonal content of adipose tissue. The actions of estrogen on sympathetic ganglia, which are key players in the browning process, are less well known. In the present study we show that ERβ influences browning of subcutaneous adipose tissue (SAT) via its actions both on sympathetic ganglia and on the SAT itself. A 3-day-treatment with a selective ERβ agonist, LY3201, induced browning of SAT in 1-year-old obese WT and ERα−/− female mice. Browning was associated with increased expression of ERβ in the nuclei of neurons in the sympathetic ganglia, increase in tyrosine hydroxylase in both nerve terminals in the SAT and sympathetic ganglia neurons and an increase of β3-adrenoceptor in the SAT. LY3201 had no effect on browning in young female or male mice. In the case of young females browning was already maximal while in males there was very little expression of ERβ in the SAT and very little expression of the β3-adrenoceptor. The increase in both sympathetic tone and responsiveness of adipocytes to catecholamines reveals a novel role for ERβ in controlling browning of adipose tissue.
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3.
  • Wu, WF, et al. (author)
  • Estrogen receptor β, a regulator of androgen receptor signaling in the mouse ventral prostate
  • 2017
  • In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 1091-6490. ; 114:19, s. E3816-E3822
  • Journal article (peer-reviewed)abstract
    • Prostate cancer is an androgen receptor (AR)-dependent disease. Goals in treatment of prostate cancer include keeping low Gleason grades low and preventing development of the lethal disease castration-resistant metastatic prostate cancer. The present study revealed that ERβ modulates AR signaling by repressing AR driver RORc and increasing AR corepressor DACH1/2. Loss of ERβ resulted in up-regulation of genes whose expression is associated with poor prognosis in prostate cancer accompanied by down-regulation of tumor-suppressive or tumor-preventive genes. Treatment of mice with an ERβ agonist resulted in the nuclear import of PTEN and repression of AR signaling. ERβ may be a promising target for treating early stage prostate cancer to prevent cancer progression.
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  • Result 1-3 of 3
Type of publication
journal article (3)
Type of content
peer-reviewed (3)
Author/Editor
Wu, WF (3)
Gustafsson, JA (2)
Warner, M (2)
Huang, B. (2)
Dai, YB (2)
Miao, YF (2)
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aut (1)
Guan, YF (1)
Nguyen, H. (1)
Barros, RPA (1)
Su, W (1)
Nadarshina, S (1)
Maneix, L (1)
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University
Karolinska Institutet (3)
Language
English (3)

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