Grant: Project Grant
University of Toronto
$1,105,425.00
Defining the regulatory mechanisms of pancreatic cancer re-growth capacity to identify effective therapy combinations
EF 2025-26
Résumé
Pancreatic cancer is a deadly disease. Currently patients with this disease are treated with chemotherapy and surgery if possible. For most patients however, their tumours regrow at some point after the initial chemotherapy. This occurs because some tumours cells in the original tumour are resistant to the chemotherapy and remain alive after treatment providing a seed for a new tumour to regrow. The effectiveness of a therapy therefore depends on both how many tumour cells a treatment initially kills and how quickly any surviving cells can regrow and form a new tumour. Different treatment schedules (amount of drug and frequency of treatments) and signals from the tumour environment impact both how well a cell can survive a therapy and how quickly it can re-grow to form a new tumour. This project proposes to explore how different drug treatments and signals from the environment change tumour cell response to therapy (initial killing and potential for tumour cell re-growth). This study will provide a basis to design new therapies for pancreatic cancer using specific combinations of drugs that maximise the number of tumour cells initially killed and minimise the capacity of any remaining tumour cells to re-grow into new tumours.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
533560
Name
McGuigan Alison P
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Biomedical Engineering 2
Projecttitle
Defining the regulatory mechanisms of pancreatic cancer re-growth capacity to identify effective therapy combinations
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$1,105,425
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Drug Tolerant Cells; In Vitro Culture Model; Pancreatic Cancer; Tissue Engineering; Tumour Microenvironment; Tumour Regrowth Dynamics; Tumour Resistance
Abstract
Pancreatic cancer is a deadly disease. Currently patients with this disease are treated with chemotherapy and surgery if possible. For most patients however, their tumours regrow at some point after the initial chemotherapy. This occurs because some tumours cells in the original tumour are resistant to the chemotherapy and remain alive after treatment providing a seed for a new tumour to regrow. The effectiveness of a therapy therefore depends on both how many tumour cells a treatment initially kills and how quickly any surviving cells can regrow and form a new tumour. Different treatment schedules (amount of drug and frequency of treatments) and signals from the tumour environment impact both how well a cell can survive a therapy and how quickly it can re-grow to form a new tumour. This project proposes to explore how different drug treatments and signals from the environment change tumour cell response to therapy (initial killing and potential for tumour cell re-growth). This study will provide a basis to design new therapies for pancreatic cancer using specific combinations of drugs that maximise the number of tumour cells initially killed and minimise the capacity of any remaining tumour cells to re-grow into new tumours.
Competitiondate
202509
Approvedterm2
5 yrs 0 mth
Pinamesdelim
McGuigan, Alison P
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,105,425~ $0~