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Grant: Collaborative Health Research Projects (NSERC partnered)

McGill University

$400,000.00

DNA Cages as a Platform for Efficient and Selective Delivery of Therapeutics into Tumor Cells

FY 2012-13

Summary
General drug cytotoxicity and drug resistance are major hurdles in traditional cancer therapies, stemming from the nonspecific delivery of cancer therapeutics to normal and cancerous cells simultaneously. We aim to develop a new method for targeted cancer therapy using non-toxic DNA cages and nanotubes. Length, diameter and composition of these DNA cages can be tuned and modified, to generate delivery molecules that can accommodate a plethora of cargo molecules, including cancer therapeutics. We have shown that DNA cages are able to accumulate in cancer cells, more specifically in drug resistant leukemia cells. We propose to encapsulate a wide range of cancer destroying molecules such as cytotoxic drugs, RNA molecules, and other cancer inhibiting agents. We propose that this novel class of cages made up of DNA bases, will evade the innate immune system, successfully and specifically deliver novel and pre-existing cancer therapeutics to cancer cells without affecting normal cells.
Program
Collaborative Health Research Projects (NSERC partnered)
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
270238
Name
Sleiman Hanadi
Region
Québec
Country
Canada
Orgtype
Research Institution; Institution Paid
Partnername
Natural Sciences and Engineering Research Council of Canada (NSERC)
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Collaborative Health Research Projects - NSERC Partnered
Projecttitle
DNA Cages as a Platform for Efficient and Selective Delivery of Therapeutics into Tumor Cells
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$400,000
Cihrequipment2
$0
Programname2
Collaborative Health Research Projects (NSERC partnered)
Keyworddelim
Anti-Apoptotic Protein Bcl-2; Antisense Oligonucleotides; Chronic Lymphocytic Leukemia; Dna Cages And Nanotubes; Drug Resistant Tumors; Enzyme-Mediated Repair Of Dna Damage; Nucleic Acid Delivery; Oligonucleotide Analogues; Sirna; Targeted Cancer Therapy
Abstract
General drug cytotoxicity and drug resistance are major hurdles in traditional cancer therapies, stemming from the nonspecific delivery of cancer therapeutics to normal and cancerous cells simultaneously. We aim to develop a new method for targeted cancer therapy using non-toxic DNA cages and nanotubes. Length, diameter and composition of these DNA cages can be tuned and modified, to generate delivery molecules that can accommodate a plethora of cargo molecules, including cancer therapeutics. We have shown that DNA cages are able to accumulate in cancer cells, more specifically in drug resistant leukemia cells. We propose to encapsulate a wide range of cancer destroying molecules such as cytotoxic drugs, RNA molecules, and other cancer inhibiting agents. We propose that this novel class of cages made up of DNA bases, will evade the innate immune system, successfully and specifically deliver novel and pre-existing cancer therapeutics to cancer cells without affecting normal cells.
Competitiondate
201210
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Sleiman, Hanadi; Panasci, Lawrence C
Approvedterm
3 ans 0 mois
Cihrcontribution2
Inst of Cancer Research~ $100,000~ $0~Institute of Genetics~ $100,000~ $0~Knowledge Translation Branch~ $200,000~ $0~
McGill University - $400,000 Grant (2012-13) | Canada Spends