Grant: Travel Awards - Institute Community Support
Direct Payment
$1,000.00
4E-T Phosphorylation by JNK Regulates P-body Assembly
FY 2012-13
Summary
The aberrant activity of several proteins has been shown to contribute to cancer development. One of these is the protein eIF4E, an important positive regulator of cancer cell growth and proliferation. When deregulated, eIF4E has been shown to promote tumour development in animal models, and to be overexpressed in several human cancers, including lymphoma, leukemia, colorectal and breast cancers. Our work focuses on 4E-T, an important regulator of eIF4E function. Several lines of evidence indicate that 4E-T interacts with eIF4E to negatively regulate its function. For this reason, 4E-T has been suggested to act as a potential tumour suppressor in cancer. We found that oxidative stress, that is often associated with cancer development, regulates the activity of 4E-T and therefore the activity of eIF4E. These findings bring important new information regarding the mechanisms that control eIF4E and cancer cell growth, and will help in the development of improved strategies for the treatment of cancer.
Department
Program
Travel Awards - Institute Community Support
Recipient
Location
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
263435
Name
Cargnello Marie
Region
Québec
Country
Canada
Orgtype
Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Institute of Cancer Research
Projecttitle
4E-T Phosphorylation by JNK Regulates P-body Assembly
Programtype2
Undefined
Orgnameinp2
Direct Payment
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Cell Signaling; Confocal Microscopy; Immunofluorescence; Immunoprecipitation; Mrna Regulation; Phosphorylation; Proteomics
Abstract
The aberrant activity of several proteins has been shown to contribute to cancer development. One of these is the protein eIF4E, an important positive regulator of cancer cell growth and proliferation. When deregulated, eIF4E has been shown to promote tumour development in animal models, and to be overexpressed in several human cancers, including lymphoma, leukemia, colorectal and breast cancers. Our work focuses on 4E-T, an important regulator of eIF4E function. Several lines of evidence indicate that 4E-T interacts with eIF4E to negatively regulate its function. For this reason, 4E-T has been suggested to act as a potential tumour suppressor in cancer. We found that oxidative stress, that is often associated with cancer development, regulates the activity of 4E-T and therefore the activity of eIF4E. These findings bring important new information regarding the mechanisms that control eIF4E and cancer cell growth, and will help in the development of improved strategies for the treatment of cancer.
Competitiondate
201205
Approvedterm2
0 yr 1 mth
Pinamesdelim
Cargnello, Marie
Approvedterm
0 an 1 mois
Cihrcontribution2
Inst of Cancer Research~ $1,000~ $0~