Androgen Receptor and Epidermal Growth Factor Signaling in Prostate Cancer Public Deposited

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  • March 19, 2019
  • Ponguta, Liliana Angelica
    • Affiliation: School of Medicine, Department of Pathology and Laboratory Medicine
  • The androgen receptor (AR) is required for prostate cancer development and contributes to tumor progression following remission in response to androgen deprivation therapy. Epidermal growth factor (EGF) increases AR transcriptional activity at low levels of androgen in the CWR-R1 prostate cancer cell line derived from the castration-recurrent CWR22 prostate cancer xenograft. Our studies indicated that EGF does not regulate TIF2 mRNA levels and that TIF2 is required for AR transactivation induced by DHT and EGF in CWR-R1 cells. Real-time RT-PCR was used to determine that hK2 is a suitable marker for androgen-regulated gene transcription in CWR-R1 cells and that DHT does not up-regulate EGF transcription. Here we report that knockdown of AR decreases EGF stimulation of prostate cancer cell growth and demonstrate a mechanistic link between EGF and AR signaling. The EGF induced increase in AR transcriptional activity is dependent on phosphorylation at MAP kinase consensus site Ser-515 in the AR NH2-terminal region and at protein kinase C consensus site Ser-578 in the AR DNA binding domain. Phosphorylation at these sites alters the nuclear-cytoplasmic shuttling of AR and AR interaction with the Ku-70/80 regulatory subunits of DNA-dependent protein kinase. Abolishing AR Ser-578 phosphorylation by introducing an S578A mutation eliminates the AR transcriptional response to EGF, increases both AR binding of Ku-70/80 and nuclear retention of AR in association with hyperphosphorylation of AR Ser-515. AR-S578A did not transactivate the MMTV-Luc reporter and we show the negative regulatory element-1 in the long terminal repeat of MMTV mediates AR-induced transcription of that promoter. The results support a model in which AR transcriptional activity increases castration-recurrent prostate cancer cell growth in response to EGF by site-specific serine phosphorylation that regulates nuclear-cytoplasmic shuttling through interactions with the Ku-70/80 regulatory complex.
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  • In Copyright
  • Wilson, Elizabeth M.
  • Open access

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