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MED12 overexpression is a frequent event in castration-resistant prostate cancer

Shaikhibrahim, Zaki (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Offermann, Anne (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Braun, Martin (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
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Menon, Roopika (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Syring, Isabella (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany; Clinic for Urology and Pediatric Urology, University Hospital of Bonn, Bonn, Germany
Nowak, Michael (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Halbach, Rebecca (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Vogel, Wenzel (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Ruiz, Christian (author)
Institute for Pathology, University Hospital Basel, Basel, Switzerland
Zellweger, Tobias (author)
Department of Urology, St. Claraspital, Basel, Switzerland
Rentsch, Cyrill A. (author)
Department of Urology, University Hospital Basel, Basel, Switzerland
Svensson, Maria, 1980- (author)
Region Örebro län,Department of Urology, Örebro University Hospital, Örebro, Sweden
Andrén, Ove, 1963- (author)
Region Örebro län,Örebro universitet, Institutionen för hälsovetenskap och medicin,Department of Urology, Örebro University Hospital, Örebro, Sweden
Bubendorf, Lukas (author)
Institute for Pathology, University Hospital Basel, Basel, Switzerland
Biskup, Saskia (author)
Center for Genomics and Transcriptomics, (CeGaT) GmbH, Tuebingen, Germany
Duensing, Stefan (author)
Section of Molecular Urooncology, Department of Urology, School of Medicine, University of Heidelberg, Heidelberg, Germany
Kirfel, Jutta (author)
Institute of Pathology, University Hospital of Bonn, Bonn, Germany
Perner, Sven (author)
Department of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany
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 (creator_code:org_t)
Bioscientifica, 2014
2014
English.
In: Endocrine-Related Cancer. - : Bioscientifica. - 1351-0088 .- 1479-6821. ; 21:4, s. 663-675
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • In a recent effort to unravel the molecular basis of prostate cancer (PCa), Barbieri and colleagues using whole-exome sequencing identified a novel recurrently mutated gene, MED12, in 5.4% of primary PCa. MED12, encoding a subunit of the Mediator complex, is a transducer of Wnt/beta-catenin signaling, linked to modulation of hedgehog signaling and to the regulation of transforming growth factor beta (TGF beta)-receptor signaling. Therefore, these studies prompted us to investigate the relevance of MED12 in PCa. Expression of MED12, SMAD3 phosphorylation, and proliferation markers was assessed by immunohistochemistry on tissue microarrays from 633 patients. siRNA-mediated knockdown of MED12 was carried out on PCa cell lines followed by cellular proliferation assays, cell cycle analysis, apoptosis assays, and treatments with recombinant TGF beta 3. We found nuclear overexpression of MED12 in 40% (28/70) of distant metastatic castration-resistant prostate cancer (CRPCMET) and 21% (19/90) of local-recurrent CRPC (CRPCLOC) in comparison with frequencies of less than 11% in androgen-sensitive PCa, and no overexpression in benign prostatic tissues. MED12 expression was significantly correlated with high proliferative activity in PCa tissues, whereas knockdown of MED12 decreased proliferation, reduced G1-to S-phase transition, and increased the expression of the cell cycle inhibitor p27. TGF beta signaling activation associates with MED12 nuclear overexpression in tissues and results in a strong increase in MED12 nuclear expression in cell lines. Furthermore, MED12 knockdown reduced the expression of the TGF beta target gene vimentin. Our findings show that MED12 nuclear overexpression is a frequent event in CRPC in comparison with androgen-sensitive PCa and is directly implicated in TGF beta signaling.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

MED12
overexpression
prostate cancer
castration-resistant
Onkologi
Oncology

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