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Grant: CIHR Fellowship

University of Ottawa

$135,000.00

Role of the Hypoxic Protein Synthesis Machinery in Human Cancer.

FY 2013-14

Summary
Historically, it is believed that human cancer cells use the same machinery as healthy cells to make proteins during tumor formation. However, our laboratory recently discovered exciting evidence suggesting that during tumour formation, cancer cells employ a unique way of producing proteins that is different from normal, healthy cells. Specifically, this mechanism becomes activated under conditions of low oxygen (hypoxia), which is a major characteristic of tumours. We have strong evidence that this unique process used by cancer cells to make proteins plays a major and clinically important role in how cancer cells survive, develop tumours, and become malignant and invasive. Here, I propose to identify and study the unique molecular components that are used specifically by human cancer cells, but not normal cells, to engage in this method of synthesizing proteins. To achieve my goal, our laboratory has developed state-of-the-art molecular techniques designed specifically to answer these important questions. I also enjoy access to a repertoire of world-class scientific resources. These unique qualities allow us to effectively engage in our project from a highly competitive vantage point, and ultimately enable us to accomplish our overarching goal of revealing fundamental molecular differences between cancer and healthy cells. The accomplishment of this goal is absolutely key to developing effective cancer therapies. The therapeutic implications of this work are tremendous and worth every effort. These studies will enable us to develop drugs that specifically target cancer cells for destruction, while leaving normal, neighbouring cells intact. Importantly, these studies represent a remarkable opportunity for us to control and prevent tumour development at early stages in humans with an extraordinary degree of cancer-specificity. Such specificity will minimize the undesirable side-effects that plaque most current cancer therapies such as chemo- and radio-therapy.
Program
CIHR Fellowship
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
300218
Name
Ho Jr Jyun D
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Role of the Hypoxic Protein Synthesis Machinery in Human Cancer.
Programtype2
Fellowship Programs
Orgnameinp2
University of Ottawa
Cihramount2
$135,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Cancer; Cancer Therapy; Eukaryotic Translation Initiation Factor 4e; Hypoxia; Hypoxia-Inducible Factor-2 Alpha; Protein Synthesis/Translation; Tumour Development
Abstract
Historically, it is believed that human cancer cells use the same machinery as healthy cells to make proteins during tumor formation. However, our laboratory recently discovered exciting evidence suggesting that during tumour formation, cancer cells employ a unique way of producing proteins that is different from normal, healthy cells. Specifically, this mechanism becomes activated under conditions of low oxygen (hypoxia), which is a major characteristic of tumours. We have strong evidence that this unique process used by cancer cells to make proteins plays a major and clinically important role in how cancer cells survive, develop tumours, and become malignant and invasive. Here, I propose to identify and study the unique molecular components that are used specifically by human cancer cells, but not normal cells, to engage in this method of synthesizing proteins. To achieve my goal, our laboratory has developed state-of-the-art molecular techniques designed specifically to answer these important questions. I also enjoy access to a repertoire of world-class scientific resources. These unique qualities allow us to effectively engage in our project from a highly competitive vantage point, and ultimately enable us to accomplish our overarching goal of revealing fundamental molecular differences between cancer and healthy cells. The accomplishment of this goal is absolutely key to developing effective cancer therapies. The therapeutic implications of this work are tremendous and worth every effort. These studies will enable us to develop drugs that specifically target cancer cells for destruction, while leaving normal, neighbouring cells intact. Importantly, these studies represent a remarkable opportunity for us to control and prevent tumour development at early stages in humans with an extraordinary degree of cancer-specificity. Such specificity will minimize the undesirable side-effects that plaque most current cancer therapies such as chemo- and radio-therapy.
Competitiondate
201311
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Ho, Jr Jyun D
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $135,000~ $0~