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Grant: Operating Grant

University of Calgary

$522,880.00

Bortezomib mediated BRCAness in Myeloma cells: novel therapeutic approach combining PARP1-2 and 26S proteasome inhibitors.

EF 2012-13

Résumé
Multiple myeloma is the second most common form of blood cancers and it remains incurable despite the addition of novel therapeutic strategies for this disease. Cancer cells invariably escape the therapeutic effect of drugs by rearranging their genetic make up overtime, an event known as genomic instability. We have identified a novel approach that takes advantage of these modifications in myeloma cells. Combining drugs that block the machinery responsible for DNA damage repair with agents that block the recycling factories, we have successfully induced catastrophic and irreversible damages that are lethal to myeloma cells. In the current research proposal we first intend to study in depth the mechanisms through the combination of these drugs induce myeloma cell death and also uncover potential mechanisms of resistance and ways to overcome them. In addition we will conduct a clinical trial to define the safety and feasibility of combining these classes of drugs in myeloma patients. We strongly believe that such approach has uncovered the Achilles heel of myeloma cells.
Programme
Operating Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
267173
Name
Bahlis Nizar J
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics
Projecttitle
Bortezomib mediated BRCAness in Myeloma cells: novel therapeutic approach combining PARP1-2 and 26S proteasome inhibitors.
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$522,880
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Multiple Myeloma; Parp And Dna Repair; Phase I Clinical Trial; Proteasome Inhibitors
Abstract
Multiple myeloma is the second most common form of blood cancers and it remains incurable despite the addition of novel therapeutic strategies for this disease. Cancer cells invariably escape the therapeutic effect of drugs by rearranging their genetic make up overtime, an event known as genomic instability. We have identified a novel approach that takes advantage of these modifications in myeloma cells. Combining drugs that block the machinery responsible for DNA damage repair with agents that block the recycling factories, we have successfully induced catastrophic and irreversible damages that are lethal to myeloma cells. In the current research proposal we first intend to study in depth the mechanisms through the combination of these drugs induce myeloma cell death and also uncover potential mechanisms of resistance and ways to overcome them. In addition we will conduct a clinical trial to define the safety and feasibility of combining these classes of drugs in myeloma patients. We strongly believe that such approach has uncovered the Achilles heel of myeloma cells.
Competitiondate
201209
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Bahlis, Nizar J
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $522,880~ $0~