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Grant: Project Grant

Centre hospitalier de l'Université de Montréal (CHUM)

$1,162,040.00

Targeting the CD73-adenosine pathway in cancer

FY 2015-16

Summary
There has been tremendous excitement over the past recent years over the development of a new form of cancer treatment that aim to stimulate the immune system. These new therapeutics consists of monoclonal antibodies that block so-called immune-checkpoints. We have discovered a new immune checkpoint that promotes tumor growth: expression of the enzyme CD73 and production of extracellular adenosine. In this proposal, we will: (i) identify a patient population most likely to benefit from adenosine-targeting therapy; (ii) develop a biomarker strategy to select and monitor patients; (iii) investigate for the first time the impact of the adenosine pathway in leukemia; (iii) use mouse genetics to assess the cell-specific roles of CD73; and (iv) assess whether adenosine-targeting therapy can synergize with other treatments.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
344349
Name
Stagg John
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Targeting the CD73-adenosine pathway in cancer
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$1,162,040
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Antibody Therapy; Breast Cancer; Her2; Immune Checkpoint; Immunotherapy; Pd-1; Targeted Therapy
Abstract
There has been tremendous excitement over the past recent years over the development of a new form of cancer treatment that aim to stimulate the immune system. These new therapeutics consists of monoclonal antibodies that block so-called immune-checkpoints. We have discovered a new immune checkpoint that promotes tumor growth: expression of the enzyme CD73 and production of extracellular adenosine. In this proposal, we will: (i) identify a patient population most likely to benefit from adenosine-targeting therapy; (ii) develop a biomarker strategy to select and monitor patients; (iii) investigate for the first time the impact of the adenosine pathway in leukemia; (iii) use mouse genetics to assess the cell-specific roles of CD73; and (iv) assess whether adenosine-targeting therapy can synergize with other treatments.
Competitiondate
201603
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Stagg, John
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,162,040~ $0~
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