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TMPRSS2-ERG gene fusion is rare compared to PTEN deletions in stage T1a prostate cancer.
Fisher, Kurt W; Zhang, Shaobo; Wang, Mingsheng; Montironi, Rodolfo; Wang, Lisha; Baldrige, Lee A; Wang, Jonas Y; MacLennan, Gregory T; Williamson, Sean R; Lopez-Beltran, Antonio; Cheng, Liang.
Afiliação
  • Fisher KW; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Zhang S; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Wang M; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Montironi R; Department of Urology, Institute of Pathological Anatomy and Histopathology, Polytechnic University of the Marche Region (Ancona), United Hospitals, Ancona, Italy.
  • Wang L; Michigan Center for Translational Pathology, University of Michigan, Ann Arbor, Michigan.
  • Baldrige LA; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Wang JY; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana.
  • MacLennan GT; Departments of Pathology and Laboratory Medicine, Case Western Reserve University, Cleveland, Ohio.
  • Williamson SR; Department of Pathology and Laboratory Medicine, Henry Ford Health System, Detroit, Michigan.
  • Lopez-Beltran A; Josephine Ford Cancer Institute, Henry Ford Health System, Detroit, Michigan.
  • Cheng L; Department of Pathology, Wayne State University School of Medicine, Detroit, Michigan.
Mol Carcinog ; 56(3): 814-820, 2017 03.
Article em En | MEDLINE | ID: mdl-27500376
ABSTRACT
T1a prostate cancers (cancer found incidentally in transurethral resection, <5% of the tissue) are indolent tumors of the transition zone. The overexpression of ERG and the inactivation of PTEN have been shown to be important drivers of carcinogenesis in large series of prostate cancer, but the genetics of transition zone tumors have not been well characterized. We evaluated the status of ERG and PTEN in formalin-fixed paraffin-embedded tissue using immunohistochemical and FISH analysis in 54 T1a transition zone tumors. The protein expression of ERG was determined using a rabbit monoclonal antibody and nuclear staining was scored as positive or negative. The genomic status of ERG was determined using three colored FISH using an ERG-TMPRSS2 tri-color probe set. The protein expression of PTEN was determined using a rabbit monoclonal antibody and cytoplasmic, and nuclear staining was scored as positive or negative. The genomic status of PTEN was determined using dual color FISH with a PTEN probe and a CEP10 probe. We found ERG rearrangement in 2 of 54 tumors (4%), one with protein overexpression by immunohistochemistry. PTEN inactivation was seen in 13 of 54 tumors (24%). Nine of the 13 PTEN alleles were inactivated by hemizygous deletion. No homozygous PTEN deletion was observed. PTEN deletion and ERG rearrangement were mutually exclusive. ERG rearrangement was rare compared to peripheral zone tumors and to PTEN inactivation in T1a transition zone tumors. © 2016 Wiley Periodicals, Inc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Proteínas de Fusão Oncogênica / Deleção de Genes / PTEN Fosfo-Hidrolase Limite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Proteínas de Fusão Oncogênica / Deleção de Genes / PTEN Fosfo-Hidrolase Limite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article