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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Published in: | British journal of cancer Vol. 116; no. 6; pp. 775 - 784 |
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Abstract | 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. |
---|---|
AbstractList | 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. 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. 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. 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. 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. 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. BACKGROUNDProstate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable predictors of aggressive tumour subtypes.METHODSWe 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.RESULTSWe 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.CONCLUSIONSOur 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. |
Author | Aprikian, Armen Whitaker, Hayley C Hamel, Lucie Dragomir, Alice Scarlata, Eleonora Brimo, Fadi Ramos-Montoya, Antonio Boufaied, Nadia Chevalier, Simone Thomson, Axel A Rochette, Annie Neal, David E |
Author_xml | – sequence: 1 givenname: Annie surname: Rochette fullname: Rochette, Annie organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 2 givenname: Nadia surname: Boufaied fullname: Boufaied, Nadia organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 3 givenname: Eleonora surname: Scarlata fullname: Scarlata, Eleonora organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 4 givenname: Lucie surname: Hamel fullname: Hamel, Lucie organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 5 givenname: Fadi surname: Brimo fullname: Brimo, Fadi organization: Department of Pathology, Division of Urology, McGill University and The McGill University Health Centre – sequence: 6 givenname: Hayley C surname: Whitaker fullname: Whitaker, Hayley C organization: Department of Oncology, University of Cambridge, Current address; Division of Surgery and Interventional Sciences, Lab 2.4, University College London, Cruciform Building, Gower Street, London, WC1E 6BT, UK – sequence: 7 givenname: Antonio surname: Ramos-Montoya fullname: Ramos-Montoya, Antonio organization: Department of Oncology, University of Cambridge, Current address; AstraZeneca, R&D Oncology iMed, Lab 240, CRUK-Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK – sequence: 8 givenname: David E surname: Neal fullname: Neal, David E organization: Department of Oncology, University of Cambridge, Current address; University of Oxford, John Radcliffe Hospital, Headley Way, Headington, Oxford OX3 9DU, UK – sequence: 9 givenname: Alice surname: Dragomir fullname: Dragomir, Alice organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 10 givenname: Armen surname: Aprikian fullname: Aprikian, Armen organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 11 givenname: Simone surname: Chevalier fullname: Chevalier, Simone organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre – sequence: 12 givenname: Axel A surname: Thomson fullname: Thomson, Axel A email: axel.thomson@mcgill.ca organization: Department of Surgery, Division of Urology, McGill University and the Cancer Research Program of the Research Institute of McGill University Health Centre |
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Keywords | prostate cancer tumour stroma stromal markers asporin |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Current address; Division of Surgery and Interventional Sciences, Lab 2.4, University College London, Cruciform Building, Gower Street, London, WC1E 6BT, UK Current address; University of Oxford, John Radcliffe Hospital, Headley Way, Headington, Oxford OX3 9DU, UK Current address; AstraZeneca, R&D Oncology iMed, Lab 240, CRUK-Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK |
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SSID | ssj0009087 |
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Snippet | Background:
Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable... Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable predictors of... Background:Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable... BACKGROUNDProstate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable... Background: Prostate cancer shows considerable heterogeneity in disease progression and we propose that markers expressed in tumour stroma may be reliable... |
SourceID | pubmedcentral proquest crossref pubmed springer |
SourceType | Open Access Repository Aggregation Database Index Database Publisher |
StartPage | 775 |
SubjectTerms | 692/4028/67/1857 692/699/2768/589/466 Adult Aged Animals Biomarkers Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Biomedical and Life Sciences Biomedicine Breast cancer Cancer Research Cells, Cultured Cohort Studies Culture Media, Conditioned - pharmacology Drug Resistance Epidemiology Extracellular Matrix Proteins - genetics Extracellular Matrix Proteins - metabolism Fetus - metabolism Fetus - pathology Fibroblasts Fibroblasts - metabolism Fibroblasts - pathology Follow-Up Studies Gene Expression Regulation, Neoplastic - drug effects Humans Immunoenzyme Techniques Male Medical research Mice Mice, Knockout Middle Aged Molecular Diagnostics Molecular Medicine Multivariate analysis Neoplasm Grading Neoplasm Recurrence, Local - genetics Neoplasm Recurrence, Local - metabolism Neoplasm Recurrence, Local - pathology Neoplasm Staging Oncology Prognosis Prostate - metabolism Prostate - pathology Prostate cancer Prostatic Neoplasms - genetics Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology Proteins Real-Time Polymerase Chain Reaction Retinoblastoma Protein - physiology Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics Stromal Cells - metabolism Stromal Cells - pathology Surveillance Survival Rate Tumor Microenvironment Tumor Suppressor Protein p53 - physiology Urology |
Title | Asporin is a stromally expressed marker associated with prostate cancer progression |
URI | https://link.springer.com/article/10.1038/bjc.2017.15 https://www.ncbi.nlm.nih.gov/pubmed/28152543 https://www.proquest.com/docview/1877377113 https://search.proquest.com/docview/1865518959 https://search.proquest.com/docview/1881762097 https://pubmed.ncbi.nlm.nih.gov/PMC5355923 |
Volume | 116 |
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