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Asporin is a stromally expressed marker associated with prostate cancer progression

BACKGROUND: Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable predictors of aggressive tumour subtypes. METHODS: We have used Kaplan–Meier, univariate and multivariate analysis to correlate the expression of...

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Autores principales: Rochette, Annie, Boufaied, Nadia, Scarlata, Eleonora, Hamel, Lucie, Brimo, Fadi, Whitaker, Hayley C, Ramos-Montoya, Antonio, Neal, David E, Dragomir, Alice, Aprikian, Armen, Chevalier, Simone, Thomson, Axel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355923/
https://www.ncbi.nlm.nih.gov/pubmed/28152543
http://dx.doi.org/10.1038/bjc.2017.15
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author Rochette, Annie
Boufaied, Nadia
Scarlata, Eleonora
Hamel, Lucie
Brimo, Fadi
Whitaker, Hayley C
Ramos-Montoya, Antonio
Neal, David E
Dragomir, Alice
Aprikian, Armen
Chevalier, Simone
Thomson, Axel A
author_facet Rochette, Annie
Boufaied, Nadia
Scarlata, Eleonora
Hamel, Lucie
Brimo, Fadi
Whitaker, Hayley C
Ramos-Montoya, Antonio
Neal, David E
Dragomir, Alice
Aprikian, Armen
Chevalier, Simone
Thomson, Axel A
author_sort Rochette, Annie
collection PubMed
description BACKGROUND: Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable predictors of aggressive tumour subtypes. METHODS: We have used Kaplan–Meier, univariate and multivariate analysis to correlate the expression of Asporin (ASPN) mRNA and protein with prostate cancer progression in independent cohorts. We used immunohistochemistry and H scoring to document stromal localisation of ASPN in a tissue microarray and mouse prostate cancer model, and correlated expression with reactive stroma, defined using Masson Trichrome staining. We used cell cultures of primary prostate cancer fibroblasts treated with serum-free conditioned media from prostate cancer cell lines to examine regulation of ASPN mRNA in tumour stromal cells. RESULTS: We observed increased expression of ASPN mRNA in a data set derived from benign vs tumour microdissected tissue, and a correlation with biochemical recurrence using Kaplan–Meier and Cox proportional hazard analysis. ASPN protein localised to tumour stroma and elevated expression of ASPN was correlated with decreased time to biochemical recurrence, in a cohort of 326 patients with a median follow up of 9.6 years. Univariate and multivariate analysis demonstrated that ASPN was correlated with progression, as were Gleason score, and clinical stage. Additionally, ASPN expression correlated with the presence of reactive stroma, suggesting that it may be a stromal marker expressed in response to the presence of tumour cells and particularly with aggressive tumour subtypes. We observed expression of ASPN in the stroma of tumours induced by p53 inhibition in a mouse model of prostate cancer, and correlation with neuroendocrine marker expression. Finally, we demonstrated that ASPN transcript expression in normal and cancer fibroblasts was regulated by conditioned media derived from the PC3, but not LNCaP, prostate cancer cell lines. CONCLUSIONS: Our results suggest that ASPN is a stromally expressed biomarker that correlates with disease progression, and is observed in reactive stroma. ASPN expression in stroma may be part of a stromal response to aggressive tumour subtypes.
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spelling pubmed-53559232017-04-04 Asporin is a stromally expressed marker associated with prostate cancer progression Rochette, Annie Boufaied, Nadia Scarlata, Eleonora Hamel, Lucie Brimo, Fadi Whitaker, Hayley C Ramos-Montoya, Antonio Neal, David E Dragomir, Alice Aprikian, Armen Chevalier, Simone Thomson, Axel A Br J Cancer Molecular Diagnostics BACKGROUND: Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable predictors of aggressive tumour subtypes. METHODS: We have used Kaplan–Meier, univariate and multivariate analysis to correlate the expression of Asporin (ASPN) mRNA and protein with prostate cancer progression in independent cohorts. We used immunohistochemistry and H scoring to document stromal localisation of ASPN in a tissue microarray and mouse prostate cancer model, and correlated expression with reactive stroma, defined using Masson Trichrome staining. We used cell cultures of primary prostate cancer fibroblasts treated with serum-free conditioned media from prostate cancer cell lines to examine regulation of ASPN mRNA in tumour stromal cells. RESULTS: We observed increased expression of ASPN mRNA in a data set derived from benign vs tumour microdissected tissue, and a correlation with biochemical recurrence using Kaplan–Meier and Cox proportional hazard analysis. ASPN protein localised to tumour stroma and elevated expression of ASPN was correlated with decreased time to biochemical recurrence, in a cohort of 326 patients with a median follow up of 9.6 years. Univariate and multivariate analysis demonstrated that ASPN was correlated with progression, as were Gleason score, and clinical stage. Additionally, ASPN expression correlated with the presence of reactive stroma, suggesting that it may be a stromal marker expressed in response to the presence of tumour cells and particularly with aggressive tumour subtypes. We observed expression of ASPN in the stroma of tumours induced by p53 inhibition in a mouse model of prostate cancer, and correlation with neuroendocrine marker expression. Finally, we demonstrated that ASPN transcript expression in normal and cancer fibroblasts was regulated by conditioned media derived from the PC3, but not LNCaP, prostate cancer cell lines. CONCLUSIONS: Our results suggest that ASPN is a stromally expressed biomarker that correlates with disease progression, and is observed in reactive stroma. ASPN expression in stroma may be part of a stromal response to aggressive tumour subtypes. Nature Publishing Group 2017-03-14 2017-02-02 /pmc/articles/PMC5355923/ /pubmed/28152543 http://dx.doi.org/10.1038/bjc.2017.15 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Rochette, Annie
Boufaied, Nadia
Scarlata, Eleonora
Hamel, Lucie
Brimo, Fadi
Whitaker, Hayley C
Ramos-Montoya, Antonio
Neal, David E
Dragomir, Alice
Aprikian, Armen
Chevalier, Simone
Thomson, Axel A
Asporin is a stromally expressed marker associated with prostate cancer progression
title Asporin is a stromally expressed marker associated with prostate cancer progression
title_full Asporin is a stromally expressed marker associated with prostate cancer progression
title_fullStr Asporin is a stromally expressed marker associated with prostate cancer progression
title_full_unstemmed Asporin is a stromally expressed marker associated with prostate cancer progression
title_short Asporin is a stromally expressed marker associated with prostate cancer progression
title_sort asporin is a stromally expressed marker associated with prostate cancer progression
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355923/
https://www.ncbi.nlm.nih.gov/pubmed/28152543
http://dx.doi.org/10.1038/bjc.2017.15
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