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Expression of CD133 in synovial sarcoma Terry, Jefferson; Nielsen, Torsten
Abstract
The development of synovial sarcoma, a translocationally defined soft tissue tumor of unknown histogenesis with considerable resistance to systemic therapy and a poor prognosis, may involve cancer stem-like cells. Recent studies suggest that synovial sarcoma arises from a primitive progenitor-type cell and have shown that synovial sarcomas contain subpopulations with enhanced tumorigenic potential; however, little is known about cancer stem-like cells in synovial sarcoma. Histologic and gene expression studies have reported features of synovial sarcoma that are reminiscent of neural development, suggesting that a neural cancer stem-like cell marker, such as CD133, may mark cancer stem-like cells in synovial sarcoma, allowing for further characterization. Here, the immunohistochemical expression of CD133 in primary synovial sarcoma tumor tissue and synovial sarcoma cell lines is determined. Subpopulations of CD133 expressing cells are present in all primary synovial sarcomas (5/5) and synovial sarcoma cell lines (3/3) examined. Histologically, CD133 positive cells are dispersed and seem to have dendritic processes. This study demonstrates the presence of CD133 expressing cells in synovial sarcoma for the first time and validates 3 synovial sarcoma cell lines as models for further study of the CD133+ subpopulation. The relationship between CD133 expression and cancer stem-like cells suggests that CD133 expressing synovial sarcoma cells may represent cancer stem-like cells in synovial sarcoma, which has significant implications for understanding the pathogenesis of this tumor and developing effective therapies.
Item Metadata
Title |
Expression of CD133 in synovial sarcoma
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Alternate Title |
CD133 in synovial sarcoma
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Creator | |
Publisher |
Lippincott Williams & Wilkins Ltd.
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Date Issued |
2010-03
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Description |
The development of synovial sarcoma, a translocationally defined soft tissue
tumor of unknown histogenesis with considerable resistance to systemic therapy and a
poor prognosis, may involve cancer stem-like cells. Recent studies suggest that
synovial sarcoma arises from a primitive progenitor-type cell and have shown that
synovial sarcomas contain subpopulations with enhanced tumorigenic potential;
however, little is known about cancer stem-like cells in synovial sarcoma. Histologic and
gene expression studies have reported features of synovial sarcoma that are
reminiscent of neural development, suggesting that a neural cancer stem-like cell
marker, such as CD133, may mark cancer stem-like cells in synovial sarcoma, allowing
for further characterization. Here, the immunohistochemical expression of CD133 in
primary synovial sarcoma tumor tissue and synovial sarcoma cell lines is determined.
Subpopulations of CD133 expressing cells are present in all primary synovial sarcomas
(5/5) and synovial sarcoma cell lines (3/3) examined. Histologically, CD133 positive
cells are dispersed and seem to have dendritic processes. This study demonstrates the
presence of CD133 expressing cells in synovial sarcoma for the first time and validates
3 synovial sarcoma cell lines as models for further study of the CD133+ subpopulation.
The relationship between CD133 expression and cancer stem-like cells suggests that
CD133 expressing synovial sarcoma cells may represent cancer stem-like cells in
synovial sarcoma, which has significant implications for understanding the pathogenesis
of this tumor and developing effective therapies.
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Subject | |
Genre | |
Type | |
Language |
eng
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Date Available |
2021-06-22
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution-NonCommercial-NoDerivatives 4.0 International
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DOI |
10.14288/1.0398485
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URI | |
Affiliation | |
Citation |
Terry, Jefferson MD, PhD; Nielsen, Torsten MD, PhD Expression of CD133 in Synovial Sarcoma, Applied Immunohistochemistry & Molecular Morphology: March 2010 - Volume 18 - Issue 2 - p 159-165
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Publisher DOI |
10.1097/PAI.0b013e3181b77451
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty
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Rights URI | |
Aggregated Source Repository |
DSpace
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Rights
Attribution-NonCommercial-NoDerivatives 4.0 International