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Grant: Project Grant

University of Guelph

$688,500.00

Understanding and exploiting hypoxic translation to selectively express therapeutic mRNAs in hypoxic tumour regions

FY 2016-17

Summary
Targeting therapies to hypoxic (low oxygen) tumour regions has been a challenge for decades. We will utilize a novel mRNA translation enhancer element to selectively express therapeutic mRNA. We will fuse therapeutic mRNAs to an enhancer sequence that will mediate their selective hypoxic expression. We will utilize several delivery strategies and nanoparticle recipes to efficiently deliver these mRNAs encapsulated in nanoparticles to hypoxic human tumours grafted onto mice. Three model cancer cell lines (glioblastoma, colorectal carcinoma and breast cancer) will be utilized in this study to show the potential to treat diverse tumour-forming cancers. Our research goals will allow for more effective and selective therapeutic targeting in cancer.
Program
Project Grant
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
356349
Name
Uniacke Jim
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Understanding and exploiting hypoxic translation to selectively express therapeutic mRNAs in hypoxic tumour regions
Programtype2
Operating Grants
Orgnameinp2
University of Guelph
Cihramount2
$688,500
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cancer; Hif; Hypoxia; Mrna; Novel Therapeutics; Rbps; Translation; Tumour Biology; Tumour Microenvironment; Xenografts
Abstract
Targeting therapies to hypoxic (low oxygen) tumour regions has been a challenge for decades. We will utilize a novel mRNA translation enhancer element to selectively express therapeutic mRNA. We will fuse therapeutic mRNAs to an enhancer sequence that will mediate their selective hypoxic expression. We will utilize several delivery strategies and nanoparticle recipes to efficiently deliver these mRNAs encapsulated in nanoparticles to hypoxic human tumours grafted onto mice. Three model cancer cell lines (glioblastoma, colorectal carcinoma and breast cancer) will be utilized in this study to show the potential to treat diverse tumour-forming cancers. Our research goals will allow for more effective and selective therapeutic targeting in cancer.
Competitiondate
201610
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Uniacke, Jim
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $688,500~ $0~