Grant: Project Grant
University of Toronto
$780,300.00
Small molecules targeting aberrant STAT3 activity: killing breast tumour cells and inducing an anti-tumour immune response.
FY 2016-17
Summary
Here, we describe a class of novel drug-like molecules that potently and selectively kill both Her2+ and triple negative breast cancer cells over normal healthy cells. These molecules target a protein called STAT3, that has been shown to play a key role in tumour progression and survival. Most excitingly, these molecules, when given to mice bearing aggressive human tumours, completely halt tumour growth, and at the same time, trigger the immune system to attack the tumour cells and accelerate the tumour clearance. We believe this represents an exciting new therapy for breast tumours with a poor prognosis. In this proposal, we aim to optimize the drug-like properties of these molecules and identify an advanced preclinical candidate for triple negative and Her2+ breast cancer.
Department
Program
Project Grant
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
355181
Name
Gunning Patrick T
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Small molecules targeting aberrant STAT3 activity: killing breast tumour cells and inducing an anti-tumour immune response.
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$780,300
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Breast Cancer Research; Drug Discovery; Her2+ Breast Cancer; Immunotherapeutic; Medicinal Chemistry; Triple Negative Breast Cancer
Abstract
Here, we describe a class of novel drug-like molecules that potently and selectively kill both Her2+ and triple negative breast cancer cells over normal healthy cells. These molecules target a protein called STAT3, that has been shown to play a key role in tumour progression and survival. Most excitingly, these molecules, when given to mice bearing aggressive human tumours, completely halt tumour growth, and at the same time, trigger the immune system to attack the tumour cells and accelerate the tumour clearance. We believe this represents an exciting new therapy for breast tumours with a poor prognosis. In this proposal, we aim to optimize the drug-like properties of these molecules and identify an advanced preclinical candidate for triple negative and Her2+ breast cancer.
Competitiondate
201610
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Gunning, Patrick T
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $780,300~ $0~