Linked Life Data

20215828

Source:http://linkedlifedata.com/resource/pubmed/id/20215828

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pubmed-article:20215828pubmed:abstractTextIntroduction: Pim1 overexpression was found to be associated with more advanced prostate cancer. Interleukin-6 (IL-6) induces Pim1 expression and is often found elevated after androgen-ablative therapy. Methods: Tumor tissue from 31 selected prostate cancer patients and cell lines were studied immunohistochemically for c-myc, Pim1, STAT3, pSTAT3-Tyr705, and androgen receptor (AR) expression. The effect of Pim1 on androgen dependence in prostate cancer was studied in transgene cell lines. Results: Pim1 expression was increased in high-grade prostate tumors (Gleason >7), irrespective of androgen status, was highest in hormone refractory prostate cancer and correlated to pSTAT3-Tyr705 expression levels. Co-expression of Pim1 and MYC was observed specifically after androgen ablation. Pim1 expression could be induced in LNCaP and PC3 cells by IL-6. Pim1 overexpression in PC3 and PNCaP increased the transcriptional activity of the AR at low levels of dihydrotestosterone. Consequently, Pim1 expression increased LNCaP cell survival specifically at castrate levels of androgen. Conclusions: Pim1 expression was increased in primary tumor samples after androgen ablation. Pim1 overexpression increased AR transcriptional activity in a ligand-dependent manner in prostate cancer cell lines, resulting in enhanced cell survival at castrate levels of androgen.lld:pubmed
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pubmed-article:20215828pubmed:authorpubmed-author:BergmanA MAMlld:pubmed
pubmed-article:20215828pubmed:authorpubmed-author:ZevenhovenJJlld:pubmed
pubmed-article:20215828pubmed:copyrightInfoCopyright (c) 2010 S. Karger AG, Basel.lld:pubmed
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pubmed-article:20215828pubmed:articleTitlePim1 regulates androgen-dependent survival signaling in prostate cancer cells.lld:pubmed
pubmed-article:20215828pubmed:affiliationDepartment of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands. h_vanderpoel @ hotmail.comlld:pubmed
pubmed-article:20215828pubmed:publicationTypeJournal Articlelld:pubmed
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