Your browser doesn't support javascript.
loading
Correlation of integrated ERG/PTEN assessment with biochemical recurrence in prostate cancer.
Brady, Lauren; Carlsson, Jessica; Baird, Anne-Marie; Casey, Orla; Vlajnic, Tatjana; Murchan, Pierre; Cormican, David; Costigan, Danielle; Gray, Steven; Sheils, Orla; O'Neill, Amanda; Watson, R William; Andren, Ove; Finn, Stephen.
Afiliação
  • Brady L; Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Carlsson J; Department of Urology, Faculty of Medicine and Health, Örebro University, Orebro, Sweden.
  • Baird AM; School of Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Casey O; Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Vlajnic T; Pathology, Institute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Switzerland.
  • Murchan P; Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Cormican D; Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Costigan D; Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Gray S; Thoracic Oncology Research Group, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Sheils O; School of Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • O'Neill A; UCD School of Medicine, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
  • Watson RW; UCD School of Medicine, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
  • Andren O; Department of Urology, Faculty of Medicine and Health, Örebro University, Orebro, Sweden.
  • Finn S; Department of Histopathology and Morbid Anatomy, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland; Department of Histopathology, St James's Hospital, Dublin, Ireland. Electronic address: Stephen.finn@tcd.ie.
Cancer Treat Res Commun ; 29: 100451, 2021.
Article em En | MEDLINE | ID: mdl-34507017
ABSTRACT

INTRODUCTION:

Prostate cancer is a heterogeneous disease, with a complex molecular landscape that evolves throughout disease progression. Common alterations in genes such as ERG and PTEN have been attributed to worse prognosis. This study aimed to further examine the clinical relevance of PTEN and ERG expression in a cohort of patients with prostate cancer post radical prostatectomy.

METHODS:

Tissue microarrays were constructed from 132 patients with prostate cancer from the Irish Prostate Cancer Research Consortium and University Hospital of Orebro, Sweden. Patients were divided into three groups - Group 1 biochemical recurrence, Group 2 no biochemical recurrence and Group 3 immediate progression after surgery. PTEN and ERG immunohistochemical analysis was performed and the association between expression levels and clinical parameters were compared.

RESULTS:

Pathological stage pT3 tumours were more common at borderline significantly higher levels amongst patients who biochemically recurred when compared to patients who did not recur after radical prostatectomy (p = 0.05). ERG and PTEN expression levels were compared separately and concurrently across all three patient groups. Lack of ERG expression was strongly associated with immediate progression after surgery (p = 0.029). Loss of/low PTEN trended towards an association with immediate progression, however this was not statistically significant (p = 0.066).

CONCLUSION:

In this study, negative ERG expression was strongly associated with immediate biochemical progression after radical prostatectomy. Moreover, a trend towards a relationship between aberrant PTEN expression and progression was observed. Additional studies with long-term follow up data may provide further clinical insight into the genomic heterogeneity in this population.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / PTEN Fosfo-Hidrolase / Recidiva Local de Neoplasia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / PTEN Fosfo-Hidrolase / Recidiva Local de Neoplasia Idioma: En Ano de publicação: 2021 Tipo de documento: Article