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Grant: Project Grant

University of British Columbia

$405,452.00

Alpha-amanitin: synthetic derivatives for applications in targeted therapy

EF 2017-18

Résumé
The deadly mushroom, A. phalloides produces a unique toxin known as amanitin that has a desired property of being able to kill both growing cells (easy) and quiescent cells (more difficult). This uniform toxicity is exciting for use in cancer therapy since not all cancer cells grow at the same rate. It is known that amanitin can be targeted to cancer by using either peptides or antibodies. However there is no viable route to synthetic amanitins and studies have relied on the natural product to develop amanitin drug conjugates. Recently we have published a total synthesis of amanitin and have become experts in its synthesis. This enables us to address the molecular pharamcology of this fascinating toxin and thereby modulate its toxicity to be directed to cancer cells.
Programme
Project Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
371282
Name
Perrin David M
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics 2
Projecttitle
Alpha-amanitin: synthetic derivatives for applications in targeted therapy
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$405,452
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Bioconjugate; Natural Product; Peptide; Targeted Therapy
Abstract
The deadly mushroom, A. phalloides produces a unique toxin known as amanitin that has a desired property of being able to kill both growing cells (easy) and quiescent cells (more difficult). This uniform toxicity is exciting for use in cancer therapy since not all cancer cells grow at the same rate. It is known that amanitin can be targeted to cancer by using either peptides or antibodies. However there is no viable route to synthetic amanitins and studies have relied on the natural product to develop amanitin drug conjugates. Recently we have published a total synthesis of amanitin and have become experts in its synthesis. This enables us to address the molecular pharamcology of this fascinating toxin and thereby modulate its toxicity to be directed to cancer cells.
Competitiondate
201709
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Perrin, David M
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $405,452~ $0~