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Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer
AIM: To investigate the expression and clinical significance of B7 homolog 3 (B7-H3) and β-1,3-galactosyltransferase-4 (B3GALT4) in colorectal cancer (CRC) patients. METHODS: Using tissue microarray, we identified the expression of B7-H3 and B3GALT4 in 223 CRC patient samples by immunohistochemistry...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102500/ https://www.ncbi.nlm.nih.gov/pubmed/30131660 http://dx.doi.org/10.3748/wjg.v24.i31.3538 |
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author | Zhang, Ting Wang, Fang Wu, Jing-Yi Qiu, Zhi-Chao Wang, Yan Liu, Fen Ge, Xiao-Song Qi, Xiao-Wei Mao, Yong Hua, Dong |
author_facet | Zhang, Ting Wang, Fang Wu, Jing-Yi Qiu, Zhi-Chao Wang, Yan Liu, Fen Ge, Xiao-Song Qi, Xiao-Wei Mao, Yong Hua, Dong |
author_sort | Zhang, Ting |
collection | PubMed |
description | AIM: To investigate the expression and clinical significance of B7 homolog 3 (B7-H3) and β-1,3-galactosyltransferase-4 (B3GALT4) in colorectal cancer (CRC) patients. METHODS: Using tissue microarray, we identified the expression of B7-H3 and B3GALT4 in 223 CRC patient samples by immunohistochemistry and evaluated the possible correlation between B7-H3 and B3GALT4 and clinical outcomes. Further, the mRNA and protein expression were identified to establish the regulatory relationship of B7-H3 with B3GALT4 in vitro. RESULTS: A significant positive correlation between B7-H3 and B3GALT4 was observed in CRC specimens (r = 0.219, P = 0.001). High expression of B7-H3 was identified as a significant independent predictor of poor overall survival (OS) [hazard ratio (HR) = 1.781; 95%CI: 1.027-3.089; P = 0.040]. Moreover, high expression of B3GALT4 was also recognized as an independent predictor of inferior OS (HR = 1.597; 95%CI: 1.007-2.533; P = 0.047). Additionally, CRC patients expressing both high B7-H3 and high B3GALT4 contributed to a significant decrease in OS (HR = 2.283; 95%CI: 1.289-4.042; P = 0.005). In CRC cell lines with stable expression of high B7-H3, the mRNA and protein expressions of B3GALT4 were significantly upregulated. Similarly, the expression of B3GALT4 was significantly reduced when expression of B7-H3 was knocked down. CONCLUSION: The expression of B3GALT4 in CRC is positively correlated with B7-H3 expression in vitro. B7-H3/B3GLAT4 may be used as dual prognostic biomarkers for CRC. |
format | Online Article Text |
id | pubmed-6102500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-61025002018-08-21 Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer Zhang, Ting Wang, Fang Wu, Jing-Yi Qiu, Zhi-Chao Wang, Yan Liu, Fen Ge, Xiao-Song Qi, Xiao-Wei Mao, Yong Hua, Dong World J Gastroenterol Basic Study AIM: To investigate the expression and clinical significance of B7 homolog 3 (B7-H3) and β-1,3-galactosyltransferase-4 (B3GALT4) in colorectal cancer (CRC) patients. METHODS: Using tissue microarray, we identified the expression of B7-H3 and B3GALT4 in 223 CRC patient samples by immunohistochemistry and evaluated the possible correlation between B7-H3 and B3GALT4 and clinical outcomes. Further, the mRNA and protein expression were identified to establish the regulatory relationship of B7-H3 with B3GALT4 in vitro. RESULTS: A significant positive correlation between B7-H3 and B3GALT4 was observed in CRC specimens (r = 0.219, P = 0.001). High expression of B7-H3 was identified as a significant independent predictor of poor overall survival (OS) [hazard ratio (HR) = 1.781; 95%CI: 1.027-3.089; P = 0.040]. Moreover, high expression of B3GALT4 was also recognized as an independent predictor of inferior OS (HR = 1.597; 95%CI: 1.007-2.533; P = 0.047). Additionally, CRC patients expressing both high B7-H3 and high B3GALT4 contributed to a significant decrease in OS (HR = 2.283; 95%CI: 1.289-4.042; P = 0.005). In CRC cell lines with stable expression of high B7-H3, the mRNA and protein expressions of B3GALT4 were significantly upregulated. Similarly, the expression of B3GALT4 was significantly reduced when expression of B7-H3 was knocked down. CONCLUSION: The expression of B3GALT4 in CRC is positively correlated with B7-H3 expression in vitro. B7-H3/B3GLAT4 may be used as dual prognostic biomarkers for CRC. Baishideng Publishing Group Inc 2018-08-21 2018-08-21 /pmc/articles/PMC6102500/ /pubmed/30131660 http://dx.doi.org/10.3748/wjg.v24.i31.3538 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Basic Study Zhang, Ting Wang, Fang Wu, Jing-Yi Qiu, Zhi-Chao Wang, Yan Liu, Fen Ge, Xiao-Song Qi, Xiao-Wei Mao, Yong Hua, Dong Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer |
title | Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer |
title_full | Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer |
title_fullStr | Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer |
title_full_unstemmed | Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer |
title_short | Clinical correlation of B7-H3 and B3GALT4 with the prognosis of colorectal cancer |
title_sort | clinical correlation of b7-h3 and b3galt4 with the prognosis of colorectal cancer |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102500/ https://www.ncbi.nlm.nih.gov/pubmed/30131660 http://dx.doi.org/10.3748/wjg.v24.i31.3538 |
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