1. Asporin is a stromally expressed marker associated with prostate cancer progression
- Author
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Armen Aprikian, Antonio Ramos-Montoya, Axel A. Thomson, Alice Dragomir, Hayley C. Whitaker, Lucie Hamel, Simone Chevalier, Eleonora Scarlata, Annie Rochette, David E. Neal, Fadi Brimo, and Nadia Boufaied
- Subjects
Male ,0301 basic medicine ,Cancer Research ,Pathology ,Retinoblastoma Protein ,Cohort Studies ,Immunoenzyme Techniques ,Mice ,Prostate cancer ,0302 clinical medicine ,Tumor Microenvironment ,Cells, Cultured ,Mice, Knockout ,Extracellular Matrix Proteins ,Tissue microarray ,Reverse Transcriptase Polymerase Chain Reaction ,Prostate ,Middle Aged ,prostate cancer ,Prognosis ,Gene Expression Regulation, Neoplastic ,Survival Rate ,Oncology ,030220 oncology & carcinogenesis ,Adult ,Biochemical recurrence ,medicine.medical_specialty ,Stromal cell ,tumour stroma ,Biology ,Real-Time Polymerase Chain Reaction ,03 medical and health sciences ,Fetus ,Stroma ,LNCaP ,Biomarkers, Tumor ,medicine ,Animals ,Humans ,RNA, Messenger ,Molecular Diagnostics ,Aged ,Neoplasm Staging ,Prostatic Neoplasms ,Asporin ,Cancer ,Fibroblasts ,medicine.disease ,030104 developmental biology ,stromal markers ,Culture Media, Conditioned ,asporin ,Neoplasm Grading ,Neoplasm Recurrence, Local ,Stromal Cells ,Tumor Suppressor Protein p53 ,Follow-Up Studies - 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.
- Published
- 2017
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