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Prognostic significance of CD168 overexpression in colorectal cancer

The expression of cluster of differentiation 168 (CD168), a cell surface receptor for hyaluronan, is associated with cancer progression and metastases. The aim of the present study was to analyze the expression of CD168 by immunohistochemistry in colorectal cancer (CRC) and to examine the associatio...

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Autores principales: Wang, Ke, Zhang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038220/
https://www.ncbi.nlm.nih.gov/pubmed/27698827
http://dx.doi.org/10.3892/ol.2016.4974
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author Wang, Ke
Zhang, Tao
author_facet Wang, Ke
Zhang, Tao
author_sort Wang, Ke
collection PubMed
description The expression of cluster of differentiation 168 (CD168), a cell surface receptor for hyaluronan, is associated with cancer progression and metastases. The aim of the present study was to analyze the expression of CD168 by immunohistochemistry in colorectal cancer (CRC) and to examine the association between CD168 expression and clinicopathological features, including survival. A total of 78 tissue specimens obtained from consecutive CRC patients exhibiting various tumor node metastasis (TNM) stages were immunostained for the analysis of CD168 expression. The prognostic value of CD168 was subsequently evaluated. Kaplan-Meier survival analysis revealed that CD168 overexpression was significantly associated with overall survival (P<0.05); however, no significant association was identified between CD168 expression and tumor location, tumor differentiation or TNM stage. Overexpression of CD168 was closely associated with poorer patient survival, which indicates that it may present a useful indicator for clinical prognosis.
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spelling pubmed-50382202016-10-03 Prognostic significance of CD168 overexpression in colorectal cancer Wang, Ke Zhang, Tao Oncol Lett Articles The expression of cluster of differentiation 168 (CD168), a cell surface receptor for hyaluronan, is associated with cancer progression and metastases. The aim of the present study was to analyze the expression of CD168 by immunohistochemistry in colorectal cancer (CRC) and to examine the association between CD168 expression and clinicopathological features, including survival. A total of 78 tissue specimens obtained from consecutive CRC patients exhibiting various tumor node metastasis (TNM) stages were immunostained for the analysis of CD168 expression. The prognostic value of CD168 was subsequently evaluated. Kaplan-Meier survival analysis revealed that CD168 overexpression was significantly associated with overall survival (P<0.05); however, no significant association was identified between CD168 expression and tumor location, tumor differentiation or TNM stage. Overexpression of CD168 was closely associated with poorer patient survival, which indicates that it may present a useful indicator for clinical prognosis. D.A. Spandidos 2016-10 2016-08-08 /pmc/articles/PMC5038220/ /pubmed/27698827 http://dx.doi.org/10.3892/ol.2016.4974 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, Ke
Zhang, Tao
Prognostic significance of CD168 overexpression in colorectal cancer
title Prognostic significance of CD168 overexpression in colorectal cancer
title_full Prognostic significance of CD168 overexpression in colorectal cancer
title_fullStr Prognostic significance of CD168 overexpression in colorectal cancer
title_full_unstemmed Prognostic significance of CD168 overexpression in colorectal cancer
title_short Prognostic significance of CD168 overexpression in colorectal cancer
title_sort prognostic significance of cd168 overexpression in colorectal cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038220/
https://www.ncbi.nlm.nih.gov/pubmed/27698827
http://dx.doi.org/10.3892/ol.2016.4974
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