Grant: Team Grant: E-Rare Joint Transnational Call
Children's Hospital of Eastern Ontario Research Institute Inc
$388,651.00
Novel therapeutic approaches to target GNE Myopathy
EF 2020-21
Résumé
GNE myopathy (GNEM) is a rare severely debilitating muscle disease which affects 1 to 9:1,000,000 people among all ethnicities, with elevated carrier rates in populations of Eastern Europe and Asian heritage, including Jewish, Persian, East Indian, Arab and Japanese. GNEM is characterized by hypo-sialylation of muscle glycoproteins, degeneration and weakness of skeletal muscles, causing severe impairment of function and quality of life. It is caused by mutations in the GNE gene which encodes synthesis of the sialic acid enzyme. There are no approved therapies and research efforts on sialylation-increasing therapies are difficult because of drug absorption and the absence of biomarkers in clinical development. These challenges are the main focus of our project. ProDGNE aims to overcome these obstacles through a unique joint collaboration among European and Canadian experts in clinical GNEM and basic research in sialic acid, organic synthesis, and -OMICS. Our developed prodrug when processed within cells becomes an active therapy, highly increasing sialic acid in GNEM patient cells and demonstrating a higher stability when compared to clinically tested drugs.
The ProDGNE consortium will develop proof of principle studies fostering early stage development for innovative therapeutic strategies tested in vitro in patient derived cells and in vivo in GNE animal models that mimic the pathological mechanism in patients. Moreover, post-translational modifications will be explored and the newly identified biomarkers, will be utilized to monitor efficacy.
Programme
Team Grant: E-Rare Joint Transnational Call
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
430847
Name
Lochmüller Hanns
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
INSERM (Bordeaux, France); German Research Foundation (Germany); Foundation for Science and Technology (Portugal); Ministero dell'ilstruzione dell'Universita e della Ricerca (Rome, Italy)
Instname2
Genetics
Theme2
Biomedical
Prcname2
Special Cases
Projecttitle
Novel therapeutic approaches to target GNE Myopathy
Programtype2
Operating Grants
Orgnameinp2
Children's Hospital of Eastern Ontario Research Institute Inc
Cihramount2
$388,651
Cihrequipment2
$0
Programname2
Team Grant: E-Rare Joint Transnational Call
Keyworddelim
Biomarkers; Glycobiology; Gne Myopathy; Innovative Therapeutic Strategies; Multi-Omic; Prodrug; Sialic Acid Pathway
Abstract
GNE myopathy (GNEM) is a rare severely debilitating muscle disease which affects 1 to 9:1,000,000 people among all ethnicities, with elevated carrier rates in populations of Eastern Europe and Asian heritage, including Jewish, Persian, East Indian, Arab and Japanese. GNEM is characterized by hypo-sialylation of muscle glycoproteins, degeneration and weakness of skeletal muscles, causing severe impairment of function and quality of life. It is caused by mutations in the GNE gene which encodes synthesis of the sialic acid enzyme. There are no approved therapies and research efforts on sialylation-increasing therapies are difficult because of drug absorption and the absence of biomarkers in clinical development. These challenges are the main focus of our project. ProDGNE aims to overcome these obstacles through a unique joint collaboration among European and Canadian experts in clinical GNEM and basic research in sialic acid, organic synthesis, and -OMICS. Our developed prodrug when processed within cells becomes an active therapy, highly increasing sialic acid in GNEM patient cells and demonstrating a higher stability when compared to clinically tested drugs.
The ProDGNE consortium will develop proof of principle studies fostering early stage development for innovative therapeutic strategies tested in vitro in patient derived cells and in vivo in GNE animal models that mimic the pathological mechanism in patients. Moreover, post-translational modifications will be explored and the newly identified biomarkers, will be utilized to monitor efficacy.
Competitiondate
202006
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Lochmüller, Hanns
Approvedterm
3 ans 0 mois
Cihrcontribution2
Institute of Genetics~ $388,651~ $0~