Grant: Operating Grant
University of British Columbia
$340,314.00
Abnormal Activation of Thymocytes High-Mobility Group Box Protein (TOX) in Cutaneous T Cell Lymphomas: Pathogenic Significance and Clinical Applications
FY 2010-11
Summary
Cutaneous T cell lymphomas (CTCL) are cancers that are developed from the CD4+ subset of the mature T lymphocytes in the skin. Although rare, these cancers are highly aggressive in advanced stages, causing high mortality because there are no curative therapies at present. These cancers are difficult to diagnose because of lack of sensitive and specific markers. Further the molecular events leading to the initiation and progression of skin lymphoma cells remain unclear.
Our laboratory recently discovered a previously unrecognized marker, TOX (which stands for thymocytes high mobility group box protein), that is abnormally activated not only in late stage disease but also in the earliest form of skin lymphomas. In the current study, we will perform a series of experiments to answer two questions: (1) Can TOX protein serve as a sensitive and specific diagnostic marker for skin lymphoma cells? Currently, the lack of such a marker is a major bottleneck in the treatment and research of skin lymphomas; and (2) Is TOX abnormal activation a cause for the development of skin lymphomas? Not only does this study have the potential of identifying a specific diagnostic marker for skin lymphomas, it also offers the unique possibility of clarifying how skin lymphomas develop, thus facilitating therapeutic development for skin lymphomas, which remain incurable at present.
Department
Program
Operating Grant
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
225786
Name
Zhou Youwen
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Clinical
Prcname2
Cancer Progression & Therapeutics 2
Projecttitle
Abnormal Activation of Thymocytes High-Mobility Group Box Protein (TOX) in Cutaneous T Cell Lymphomas: Pathogenic Significance and Clinical Applications
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$340,314
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Cutaneous T Cell Lymphoma; Epigenomics; Molecular Disease Markers; Sezary Cells; Sezary Syndrome; T Cell Development; Tox
Abstract
Cutaneous T cell lymphomas (CTCL) are cancers that are developed from the CD4+ subset of the mature T lymphocytes in the skin. Although rare, these cancers are highly aggressive in advanced stages, causing high mortality because there are no curative therapies at present. These cancers are difficult to diagnose because of lack of sensitive and specific markers. Further the molecular events leading to the initiation and progression of skin lymphoma cells remain unclear.
Our laboratory recently discovered a previously unrecognized marker, TOX (which stands for thymocytes high mobility group box protein), that is abnormally activated not only in late stage disease but also in the earliest form of skin lymphomas. In the current study, we will perform a series of experiments to answer two questions: (1) Can TOX protein serve as a sensitive and specific diagnostic marker for skin lymphoma cells? Currently, the lack of such a marker is a major bottleneck in the treatment and research of skin lymphomas; and (2) Is TOX abnormal activation a cause for the development of skin lymphomas? Not only does this study have the potential of identifying a specific diagnostic marker for skin lymphomas, it also offers the unique possibility of clarifying how skin lymphomas develop, thus facilitating therapeutic development for skin lymphomas, which remain incurable at present.
Competitiondate
201103
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Zhou, Youwen
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $340,314~ $0~