Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes

Prostate cancer is the second leading cause of cancer-related death. The androgen deprivation therapy is the standard treatment for advanced stages. Unfortunately, virtually all tumors become resistant to androgen withdrawal. The progression to castration-resistance is not fully understood, although...

Full description

Bibliographic Details
Main Authors: Bruno Jim Rocca, Alessandro Ginori, Aurora Barone, Calogera Calandra, Filippo Crivelli, Giulia De Falco, Sara Gazaneo, Sergio Tripodi, Gabriele Cevenini, Maria Teresa del Vecchio, Maria Raffaella Ambrosio, Piero Tosi
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2015/985950
id doaj-417e7f54afb74957a9b217a948310ba0
record_format Article
spelling doaj-417e7f54afb74957a9b217a948310ba02020-11-24T23:24:09ZengHindawi LimitedBioMed Research International2314-61332314-61412015-01-01201510.1155/2015/985950985950Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related ChangesBruno Jim Rocca0Alessandro Ginori1Aurora Barone2Calogera Calandra3Filippo Crivelli4Giulia De Falco5Sara Gazaneo6Sergio Tripodi7Gabriele Cevenini8Maria Teresa del Vecchio9Maria Raffaella Ambrosio10Piero Tosi11Section of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Ospedale di Circolo di Busto Arsizio, Presidio Ospedaliero di Saronno, Piazzale Borella 1, 21047 Saronno, ItalySection of Pathology, Ospedale di Circolo di Busto Arsizio, Presidio Ospedaliero di Saronno, Piazzale Borella 1, 21047 Saronno, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Azienda Ospedaliera Universitaria Senese, Viale Bracci 16, 53100 Siena, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalyDepartment of Medicine, Science and Neurosciences, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalySection of Pathology, Department of Medical Biotechnology, University of Siena, Via delle Scotte 6, 53100 Siena, ItalyProstate cancer is the second leading cause of cancer-related death. The androgen deprivation therapy is the standard treatment for advanced stages. Unfortunately, virtually all tumors become resistant to androgen withdrawal. The progression to castration-resistance is not fully understood, although a recent paper has suggested translationally controlled tumor protein to be implicated in the process. The present study was designed to investigate the role of this protein in prostate cancer, focusing on the correlation between its expression level with tumor differentiation and response to treatment. We retrieved 292 prostatic cancer specimens; of these 153 had been treated only by radical prostatectomy and 139 had undergone radical prostatectomy after neoadjuvant treatment with combined androgen blockade therapy. Non-neoplastic controls were represented by 102 prostatic peripheral zone specimens. In untreated patients, the expression of the protein, evaluated by RT-qPCR and immunohistochemistry, was significantly higher in tumor specimens than in non-neoplastic control, increasing as Gleason pattern and score progressed. In treated prostates, the staining was correlated with the response to treatment. An association between protein expression and the main clinicopathological factors involved in prostate cancer aggressiveness was identified. These findings suggest that the protein may be a promising prognostic factor and a target for therapy.http://dx.doi.org/10.1155/2015/985950
collection DOAJ
language English
format Article
sources DOAJ
author Bruno Jim Rocca
Alessandro Ginori
Aurora Barone
Calogera Calandra
Filippo Crivelli
Giulia De Falco
Sara Gazaneo
Sergio Tripodi
Gabriele Cevenini
Maria Teresa del Vecchio
Maria Raffaella Ambrosio
Piero Tosi
spellingShingle Bruno Jim Rocca
Alessandro Ginori
Aurora Barone
Calogera Calandra
Filippo Crivelli
Giulia De Falco
Sara Gazaneo
Sergio Tripodi
Gabriele Cevenini
Maria Teresa del Vecchio
Maria Raffaella Ambrosio
Piero Tosi
Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes
BioMed Research International
author_facet Bruno Jim Rocca
Alessandro Ginori
Aurora Barone
Calogera Calandra
Filippo Crivelli
Giulia De Falco
Sara Gazaneo
Sergio Tripodi
Gabriele Cevenini
Maria Teresa del Vecchio
Maria Raffaella Ambrosio
Piero Tosi
author_sort Bruno Jim Rocca
title Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes
title_short Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes
title_full Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes
title_fullStr Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes
title_full_unstemmed Translationally Controlled Tumor Protein in Prostatic Adenocarcinoma: Correlation with Tumor Grading and Treatment-Related Changes
title_sort translationally controlled tumor protein in prostatic adenocarcinoma: correlation with tumor grading and treatment-related changes
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2015-01-01
description Prostate cancer is the second leading cause of cancer-related death. The androgen deprivation therapy is the standard treatment for advanced stages. Unfortunately, virtually all tumors become resistant to androgen withdrawal. The progression to castration-resistance is not fully understood, although a recent paper has suggested translationally controlled tumor protein to be implicated in the process. The present study was designed to investigate the role of this protein in prostate cancer, focusing on the correlation between its expression level with tumor differentiation and response to treatment. We retrieved 292 prostatic cancer specimens; of these 153 had been treated only by radical prostatectomy and 139 had undergone radical prostatectomy after neoadjuvant treatment with combined androgen blockade therapy. Non-neoplastic controls were represented by 102 prostatic peripheral zone specimens. In untreated patients, the expression of the protein, evaluated by RT-qPCR and immunohistochemistry, was significantly higher in tumor specimens than in non-neoplastic control, increasing as Gleason pattern and score progressed. In treated prostates, the staining was correlated with the response to treatment. An association between protein expression and the main clinicopathological factors involved in prostate cancer aggressiveness was identified. These findings suggest that the protein may be a promising prognostic factor and a target for therapy.
url http://dx.doi.org/10.1155/2015/985950
work_keys_str_mv AT brunojimrocca translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT alessandroginori translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT aurorabarone translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT calogeracalandra translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT filippocrivelli translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT giuliadefalco translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT saragazaneo translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT sergiotripodi translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT gabrielecevenini translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT mariateresadelvecchio translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT mariaraffaellaambrosio translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
AT pierotosi translationallycontrolledtumorproteininprostaticadenocarcinomacorrelationwithtumorgradingandtreatmentrelatedchanges
_version_ 1725561437720412160