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Grant: Operating Grant

McGill University

$913,610.00

Allosteric Regulation and Biased Signaling of Prostaglandin F2alpha receptors.

EF 2011-12

Résumé
Our research focuses on a class of membrane receptor, for molecules called prostaglandins involved in premature birth and some forms of cancer (e.g. colorectal, endometrial). Pharmacological therapies targeting these receptors would greatly reduce the personal and socio-economical burden associated with these problems. Our research has unveiled the properties of a new class of drugs that act in an unconventional way on these receptors to selectively affect the response of the natural hormone. We propose to characterize the functional domains of these receptors, known as "allosteric" sites, targeted by our newly discovered compounds, to iteratively generate more selective and efficacious drugs. Our research should have great impact on managing pre-term labour, which is associated with more than 75% of neonate mortality, as well as in the treatment of endometrial and colon cancers which have a 20% rate in mortality among women, and represent the second leading cause of cancer-related death among Canadians, respectively.
Programme
Operating Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
252340
Name
Laporte Stéphane A
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Gender and Health
Theme2
Biomedical
Prcname2
Pharmacology & Toxicology
Projecttitle
Allosteric Regulation and Biased Signaling of Prostaglandin F2alpha receptors.
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$913,610
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Allosteric And Biased Signaling; Cancer; Drug Development; G Protein-Coupled Receptors; Molecular Pharmacoloy; Pre-Term Delivery; Prostaglandin
Abstract
Our research focuses on a class of membrane receptor, for molecules called prostaglandins involved in premature birth and some forms of cancer (e.g. colorectal, endometrial). Pharmacological therapies targeting these receptors would greatly reduce the personal and socio-economical burden associated with these problems. Our research has unveiled the properties of a new class of drugs that act in an unconventional way on these receptors to selectively affect the response of the natural hormone. We propose to characterize the functional domains of these receptors, known as "allosteric" sites, targeted by our newly discovered compounds, to iteratively generate more selective and efficacious drugs. Our research should have great impact on managing pre-term labour, which is associated with more than 75% of neonate mortality, as well as in the treatment of endometrial and colon cancers which have a 20% rate in mortality among women, and represent the second leading cause of cancer-related death among Canadians, respectively.
Competitiondate
201203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Laporte, Stéphane A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $913,610~ $0~