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PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma

INTRODUCTION: CD44 has been proposed as a prognostic marker and a stem cell marker but studies in patients with prostate cancer have yielded inconsistent results. PATIENTS AND METHODS: Patients submitted to radical prostatectomy between 2008 and 2013 at a university hospital were followed with biann...

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Autores principales: Hirth, Carlos Gustavo, dos Santos, Adriele Machado, de Cerqueira, João Batista Gadelha, Jamacaru, Francisco Vagnaldo Fechine, da Cunha, Maria do Perpétuo Socorro Saldanha, Dornelas, Conceição Aparecida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846379/
https://www.ncbi.nlm.nih.gov/pubmed/29682524
http://dx.doi.org/10.1155/2018/2061268
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author Hirth, Carlos Gustavo
dos Santos, Adriele Machado
de Cerqueira, João Batista Gadelha
Jamacaru, Francisco Vagnaldo Fechine
da Cunha, Maria do Perpétuo Socorro Saldanha
Dornelas, Conceição Aparecida
author_facet Hirth, Carlos Gustavo
dos Santos, Adriele Machado
de Cerqueira, João Batista Gadelha
Jamacaru, Francisco Vagnaldo Fechine
da Cunha, Maria do Perpétuo Socorro Saldanha
Dornelas, Conceição Aparecida
author_sort Hirth, Carlos Gustavo
collection PubMed
description INTRODUCTION: CD44 has been proposed as a prognostic marker and a stem cell marker but studies in patients with prostate cancer have yielded inconsistent results. PATIENTS AND METHODS: Patients submitted to radical prostatectomy between 2008 and 2013 at a university hospital were followed with biannual serum PSA tests to determine the biochemical recurrence (BR). Archived paraffin blocks with neoplastic and nonneoplastic tissue were evaluated immunohistochemically for a panCD44 and MYC. RESULTS: Sixty-nine patients completed follow-up and were included. CD44 positivity was observed in inflammatory cells (42%), nonneoplastic epithelium (39.7%), and neoplastic tissue (12.3%). In nonneoplastic tissues staining was observed in basal and luminal cells with the morphology of terminally differentiated cells. In neoplastic tissues, CD44 negativity was correlated with higher Gleason scores (Rho = −0.204; p = 0.042) and higher preoperative serum PSA levels when evaluated continuously (p = 0.029). CD44 expression was not associated with tumor stage (p = 0.668), surgical margin status (p = 0.471), or BR (p = 0.346), nor was there any association between CD44 and MYC expression in neoplastic tissue (p = 1.0). CONCLUSION: In the bulk of cells, the minority of cancer stem cells would not be detected by immunohistochemistry using panCD44. As a prognostic marker, its expression was weakly correlated with Gleason score and preoperative PSA level, but not with surgical margin status, tumor stage, or BR.
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spelling pubmed-58463792018-04-22 PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma Hirth, Carlos Gustavo dos Santos, Adriele Machado de Cerqueira, João Batista Gadelha Jamacaru, Francisco Vagnaldo Fechine da Cunha, Maria do Perpétuo Socorro Saldanha Dornelas, Conceição Aparecida Biomed Res Int Research Article INTRODUCTION: CD44 has been proposed as a prognostic marker and a stem cell marker but studies in patients with prostate cancer have yielded inconsistent results. PATIENTS AND METHODS: Patients submitted to radical prostatectomy between 2008 and 2013 at a university hospital were followed with biannual serum PSA tests to determine the biochemical recurrence (BR). Archived paraffin blocks with neoplastic and nonneoplastic tissue were evaluated immunohistochemically for a panCD44 and MYC. RESULTS: Sixty-nine patients completed follow-up and were included. CD44 positivity was observed in inflammatory cells (42%), nonneoplastic epithelium (39.7%), and neoplastic tissue (12.3%). In nonneoplastic tissues staining was observed in basal and luminal cells with the morphology of terminally differentiated cells. In neoplastic tissues, CD44 negativity was correlated with higher Gleason scores (Rho = −0.204; p = 0.042) and higher preoperative serum PSA levels when evaluated continuously (p = 0.029). CD44 expression was not associated with tumor stage (p = 0.668), surgical margin status (p = 0.471), or BR (p = 0.346), nor was there any association between CD44 and MYC expression in neoplastic tissue (p = 1.0). CONCLUSION: In the bulk of cells, the minority of cancer stem cells would not be detected by immunohistochemistry using panCD44. As a prognostic marker, its expression was weakly correlated with Gleason score and preoperative PSA level, but not with surgical margin status, tumor stage, or BR. Hindawi 2018-02-26 /pmc/articles/PMC5846379/ /pubmed/29682524 http://dx.doi.org/10.1155/2018/2061268 Text en Copyright © 2018 Carlos Gustavo Hirth et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hirth, Carlos Gustavo
dos Santos, Adriele Machado
de Cerqueira, João Batista Gadelha
Jamacaru, Francisco Vagnaldo Fechine
da Cunha, Maria do Perpétuo Socorro Saldanha
Dornelas, Conceição Aparecida
PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma
title PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma
title_full PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma
title_fullStr PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma
title_full_unstemmed PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma
title_short PanCD44 Immunohistochemical Evaluation in Prostatectomies from Patients with Adenocarcinoma
title_sort pancd44 immunohistochemical evaluation in prostatectomies from patients with adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846379/
https://www.ncbi.nlm.nih.gov/pubmed/29682524
http://dx.doi.org/10.1155/2018/2061268
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