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Grant: CIHR New Investigator

University of Victoria (British Columbia)

$300,000.00

Small molecule probes and disruptors of lysine methylation pathways

EF 2009-10

Résumé
The growth and survival of cancer cells are governed by cellular signaling networks built on a framework of protein-protein interactions. One such interaction, the binding of a DNA-associated protein called H3K27me3 with another partner called polycomb, has been shown to shut down the operation of several cellular control circuits that normally serve to prevent abnormal cell growth. The results is catastrophic... cells in which this interaction is occurring can become cancer cells of many different varieties (breast, prostate, brain, blood, and many more). We have discovered a chemical that stops this interaction from occurring. It is the only chemical that has ever been reported that stops H3K27me3 and polycomb from binding to each other. We are asking for funding to further develop this investigative lead into more potent and more selective versions. The cancer research community has flagged this type of interaction as the target for "cancer treatments of the future," and we hope that our exploration of the potency and activity of our new compounds will form the basis for the future development of an entirely new classes of cancer therapies.
Programme
CIHR New Investigator
Emplacement
British Columbia, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
191986
Name
Hof Fraser
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
New Investigators C
Projecttitle
Small molecule probes and disruptors of lysine methylation pathways
Programtype2
Salary Programs
Orgnameinp2
University of Victoria (British Columbia)
Cihramount2
$300,000
Cihrequipment2
$0
Programname2
CIHR New Investigator
Keyworddelim
Ezh2 And Cancer; Gene Regulation; Histones; Post-Translational Methylation; Protein-Protein Interactions; Targeted Therapies
Abstract
The growth and survival of cancer cells are governed by cellular signaling networks built on a framework of protein-protein interactions. One such interaction, the binding of a DNA-associated protein called H3K27me3 with another partner called polycomb, has been shown to shut down the operation of several cellular control circuits that normally serve to prevent abnormal cell growth. The results is catastrophic... cells in which this interaction is occurring can become cancer cells of many different varieties (breast, prostate, brain, blood, and many more). We have discovered a chemical that stops this interaction from occurring. It is the only chemical that has ever been reported that stops H3K27me3 and polycomb from binding to each other. We are asking for funding to further develop this investigative lead into more potent and more selective versions. The cancer research community has flagged this type of interaction as the target for "cancer treatments of the future," and we hope that our exploration of the potency and activity of our new compounds will form the basis for the future development of an entirely new classes of cancer therapies.
Competitiondate
200909
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Hof, Fraser
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $300,000~ $0~