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Regulation of interleukin‐6‐mediated PI3K activation and neuroendocrine differentiation by androgen signaling in prostate cancer LNCaP cells
Author(s) -
Xie Shaozhen,
Lin HuiKuan,
Ni Jing,
Yang Lin,
Wang Liang,
di Sant'Agnese P. Anthony,
Chang Chawnshang
Publication year - 2004
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.20048
Subject(s) - lncap , androgen receptor , neuroendocrine differentiation , prostate cancer , androgen , cancer research , pi3k/akt/mtor pathway , biology , endocrinology , medicine , signal transduction , microbiology and biotechnology , cancer , hormone
BACKGROUND Neuroendocrine (NE) differentiation in prostate cancer has been suggested to be one of the early events in the development of androgen independence. In the human prostate cancer LNCaP cell line, treatment with interleukin‐6 (IL‐6) induces NE‐like differentiation, which is similar to the phenomena observed in advanced stages of prostate cancer progression. In this study, we investigate how androgen plays a role in IL‐6‐mediated NE differentiation in LNCaP cell line. METHODS Western blot, co‐immunoprecipitation (co‐IP), and GST pull‐down assays were performed to detect the protein expression and protein–protein interaction. PI3K kinase assay was used to measure PI3K activity. RESULTS Addition of androgen blocks IL‐6‐mediated PI3K activation and NE differentiation in LNCaP cells. In vivo and in vitro protein interaction assays suggested that androgen receptor (AR) can directly interact with IL‐6 transducer gp130. In addition, androgen treatment enhances the interaction between AR and gp130, interrupts the IL‐6‐induced gp130‐mediated PI3K activation, which may lead to inhibition of IL‐6‐mediated NE differentiation in LNCaP cells. CONCLUSIONS Our results suggest androgen and AR can regulate IL‐6‐mediated LNCaP cell NE differentiation via directly modulating the IL‐6‐PI3K pathway. © 2004 Wiley‐Liss, Inc.