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Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships

University of Alberta

$105,000.00

The suppression of DNA mismatch repair by the oncoprotein NPM-ALK.

FY 2011-12

Summary
There are many mechanisms known to contribute to cancer formation, one of which is related to a group of proteins called tyrosine kinases. In normal cells, tyrosine kinases are known to play key roles in regulating many important cellular functions. In some cancer cells, tyrosine kinases are over-active, thereby altering a wide range of cellular processes and often leading to uncontrolled cell growth and tumor formation. Our research group has been studying a cancer-forming tyrosine kinase called NPM-ALK for the past 9 years. Recently, we discovered for the first time that NPM-ALK can induce a cellular abnormality called genetic instability by interfering with a critical cellular function known as DNA mismatch repair. DNA mismatch repair normally functions to safeguard the integrity of our genes and protect them from potentially harmful mutations. Genetic instability is often a key feature seen in many types of cancer. The main purpose of this study is to investigate this novel cancer promoting mechanism and to further our understanding of how tyrosine kinases, when aberrantly over-active, can alter the capacity for the cell to undergo successful DNA mismatch repair. In the future, we aim to develop new therapeutic approaches based on the new information derived from this study.
Program
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
257399
Name
Bone Kathleen M
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
The suppression of DNA mismatch repair by the oncoprotein NPM-ALK.
Programtype2
Studentship Programs
Orgnameinp2
University of Alberta
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Dna Mismatch Repair; Immunoblotting; Immunoprecipitation; Lymphoma; Oncogenic Tyrosine Kinase; Post-Translational Modification; Protein Function; Site-Directed Mutagenesis; Tissue Culture; Tumorigenesis
Abstract
There are many mechanisms known to contribute to cancer formation, one of which is related to a group of proteins called tyrosine kinases. In normal cells, tyrosine kinases are known to play key roles in regulating many important cellular functions. In some cancer cells, tyrosine kinases are over-active, thereby altering a wide range of cellular processes and often leading to uncontrolled cell growth and tumor formation. Our research group has been studying a cancer-forming tyrosine kinase called NPM-ALK for the past 9 years. Recently, we discovered for the first time that NPM-ALK can induce a cellular abnormality called genetic instability by interfering with a critical cellular function known as DNA mismatch repair. DNA mismatch repair normally functions to safeguard the integrity of our genes and protect them from potentially harmful mutations. Genetic instability is often a key feature seen in many types of cancer. The main purpose of this study is to investigate this novel cancer promoting mechanism and to further our understanding of how tyrosine kinases, when aberrantly over-active, can alter the capacity for the cell to undergo successful DNA mismatch repair. In the future, we aim to develop new therapeutic approaches based on the new information derived from this study.
Competitiondate
201110
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Bone, Kathleen M
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~