Grant: Project Grant
University of British Columbia
$956,250.00
Stromal Gene Expression Predicts And May Drive Metastasis in Prostate Cancer
EF 2016-17
Résumé
Men with low to intermediate risk prostate cancer (PCa) face vexing decisions regarding treatment. The tumour can remain indolent and will not impact the patient within his lifetime, or it can progress to become life threatening (metastatic tumour). A holy grail of PCa research is the identification of prognostic biomarkers, which are biological factors that are associated with the disease outcomes, that can be used to improve patient risk stratification at time of diagnosis and guide treatment decisions. We have created patient-derived PCa tumour mouse models with different metastatic potential that fully recapitulate the transition of a patient tumour from indolence to metastasis. In an effort to identify the mechanisms that drive the growth of a metastatic tumour in these models, we have identified a rich source of prognostic biomarkers in the mouse stroma, which is the tissue supporting tumour growth. We have been able to identify a group of 93 genes only active in the mouse stroma associated with metastasis. We called this group of genes the Stromal Metastatic Signature or SMS. In collaboration with GenomeDx Biosciences, a Vancouver-based company, we confirmed our preliminary observations; that the SMS is strongly prognostic for predicting metastasis in human tumour. The purpose of this very innovative proposal is to seek funding first to further validate the SMS using additional large human tumour cohorts, second to improve the SMS prognostic value by integrating existing tumour-based signatures, and finally to test the hypothesis that the stromal compartment drives metastasis using a novel therapeutic agent developed in our research centre. This very innovative project represents a unique opportunity to apply novel and exciting research findings to the advancement of an important health issue.
Programme
Project Grant
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
356793
Name
Collins Colin C
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Clinical
Prcname2
Project Grant Competition
Projecttitle
Stromal Gene Expression Predicts And May Drive Metastasis in Prostate Cancer
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$956,250
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Biomarkers; Gene Signature; Metastasis; Patient-Derived Xenografts; Prostate Cancer; Risk Stratification; Stromal Cell; Whole Genome Sequencing; Whole Transcriptome Sequencing
Abstract
Men with low to intermediate risk prostate cancer (PCa) face vexing decisions regarding treatment. The tumour can remain indolent and will not impact the patient within his lifetime, or it can progress to become life threatening (metastatic tumour). A holy grail of PCa research is the identification of prognostic biomarkers, which are biological factors that are associated with the disease outcomes, that can be used to improve patient risk stratification at time of diagnosis and guide treatment decisions. We have created patient-derived PCa tumour mouse models with different metastatic potential that fully recapitulate the transition of a patient tumour from indolence to metastasis. In an effort to identify the mechanisms that drive the growth of a metastatic tumour in these models, we have identified a rich source of prognostic biomarkers in the mouse stroma, which is the tissue supporting tumour growth. We have been able to identify a group of 93 genes only active in the mouse stroma associated with metastasis. We called this group of genes the Stromal Metastatic Signature or SMS. In collaboration with GenomeDx Biosciences, a Vancouver-based company, we confirmed our preliminary observations; that the SMS is strongly prognostic for predicting metastasis in human tumour. The purpose of this very innovative proposal is to seek funding first to further validate the SMS using additional large human tumour cohorts, second to improve the SMS prognostic value by integrating existing tumour-based signatures, and finally to test the hypothesis that the stromal compartment drives metastasis using a novel therapeutic agent developed in our research centre. This very innovative project represents a unique opportunity to apply novel and exciting research findings to the advancement of an important health issue.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Collins, Colin C; Daugaard, Mads; Wang, Yuzhuo
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $956,250~ $0~