Grant: Project Grant
University of Toronto
$898,875.00
Identification and characterization of microRNAs essential for the development and fitness of chemoresistant AML
EF 2020-21
Résumé
Drug resistance in patients with acute myeloid leukemia (AML) is a major hurdle for successful therapy. MicroRNA (miRNA) are small RNA with critical roles in most cellular processes that can be disrupted to promote diverse diseases. Aberrant miRNA expression has been implicated in the development and maintenance of AML, however little is known about the specific role and clinical utility for miRNA in AML chemoresistance. The overarching goal of this project is to characterize miRNA that drive and maintain chemoresistant AML as novel actionable targets in AML therapies. We have developed advanced cellular and molecular tools, novel bioinformatic approaches and access to human samples that will allow us to identify and validate miRNA that are critical for chemoresistance. Our efforts represent fundamental work required to identify novel microRNA-associated therapeutic strategies to improve treatments for AML.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
433601
Name
Salmena Leonardo L
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics 2
Projecttitle
Identification and characterization of microRNAs essential for the development and fitness of chemoresistant AML
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$898,875
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Aml; Chemoresistance; Crispr Functional Screens; Microrna; Mirrna-Seq
Abstract
Drug resistance in patients with acute myeloid leukemia (AML) is a major hurdle for successful therapy. MicroRNA (miRNA) are small RNA with critical roles in most cellular processes that can be disrupted to promote diverse diseases. Aberrant miRNA expression has been implicated in the development and maintenance of AML, however little is known about the specific role and clinical utility for miRNA in AML chemoresistance. The overarching goal of this project is to characterize miRNA that drive and maintain chemoresistant AML as novel actionable targets in AML therapies. We have developed advanced cellular and molecular tools, novel bioinformatic approaches and access to human samples that will allow us to identify and validate miRNA that are critical for chemoresistance. Our efforts represent fundamental work required to identify novel microRNA-associated therapeutic strategies to improve treatments for AML.
Competitiondate
202010
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Salmena, Leonardo L
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $898,875~ $0~