蛋白激酶B
雄激素受体
前列腺癌
癌症研究
PI3K/AKT/mTOR通路
雄激素
前列腺
细胞生长
内科学
生物
LNCaP公司
内分泌学
信号转导
癌症
化学
医学
细胞生物学
激素
生物化学
作者
Yong Wen,Mickey C.‐T. Hu,Keishi Makino,Bill Spohn,Geoffrey Bartholomeusz,Duen‐Hwa Yan,Mien‐Chie Hung
出处
期刊:PubMed
[National Institutes of Health]
日期:2000-12-15
卷期号:60 (24): 6841-5
被引量:463
摘要
HER-2/neu has been implicated in the activation of androgen receptor (AR) and in inducing hormone-independent prostate cancer growth. Here we report that HER-2/neu activates Akt (protein kinase B) to promote prostate cancer cell survival and growth in the absence of androgen. Blocking of the Akt pathway by a dominant-negative Akt or an inhibitor LY294002 abrogates the HER-2/neu-induced AR signaling and cell survival/growth effects in the absence or presence of androgen. Akt specifically binds to AR and phosphorylates serines 213 and 791 of AR. Thus, Akt is a novel activator of AR required for HER-2/neu signaling to androgen-independent survival and growth of prostate cancer cells.
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