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Upregulation of the B7/CD28 family member B7-H3 in bladder cancer

Dysregulation of B7-H3 has been observed in a variety of types of human cancers. In the present study, the mRNA expression level of B7-H3 was analyzed in bladder cancer by performing semi-quantitative reverse transcription-polymerase chain reaction on clinical specimens from transitional cell carcin...

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Detalles Bibliográficos
Autores principales: WU, DEYAO, ZHANG, ZICHUN, PAN, HUIXING, FAN, YUANFENG, QU, PING, ZHOU, JIAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314980/
https://www.ncbi.nlm.nih.gov/pubmed/25663925
http://dx.doi.org/10.3892/ol.2014.2828
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author WU, DEYAO
ZHANG, ZICHUN
PAN, HUIXING
FAN, YUANFENG
QU, PING
ZHOU, JIAN
author_facet WU, DEYAO
ZHANG, ZICHUN
PAN, HUIXING
FAN, YUANFENG
QU, PING
ZHOU, JIAN
author_sort WU, DEYAO
collection PubMed
description Dysregulation of B7-H3 has been observed in a variety of types of human cancers. In the present study, the mRNA expression level of B7-H3 was analyzed in bladder cancer by performing semi-quantitative reverse transcription-polymerase chain reaction on clinical specimens from transitional cell carcinomas (TCCs) and their normal adjacent tissues (NATs). Immunohistochemical analysis was performed to compare the protein expression level of B7-H3 in TCCs and the paired NATs. The present study indicated that the B7-H3 mRNA expression level was significantly higher in the TCC samples compared with the paired NAT samples. Furthermore, immunohistochemical analyses indicated that the B7-H3 protein expression level was significantly upregulated in the TCC samples compared with in the paired NAT samples, indicating that B7-H3 dysregulation may be important in the progression of bladder cancer.
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spelling pubmed-43149802015-02-06 Upregulation of the B7/CD28 family member B7-H3 in bladder cancer WU, DEYAO ZHANG, ZICHUN PAN, HUIXING FAN, YUANFENG QU, PING ZHOU, JIAN Oncol Lett Articles Dysregulation of B7-H3 has been observed in a variety of types of human cancers. In the present study, the mRNA expression level of B7-H3 was analyzed in bladder cancer by performing semi-quantitative reverse transcription-polymerase chain reaction on clinical specimens from transitional cell carcinomas (TCCs) and their normal adjacent tissues (NATs). Immunohistochemical analysis was performed to compare the protein expression level of B7-H3 in TCCs and the paired NATs. The present study indicated that the B7-H3 mRNA expression level was significantly higher in the TCC samples compared with the paired NAT samples. Furthermore, immunohistochemical analyses indicated that the B7-H3 protein expression level was significantly upregulated in the TCC samples compared with in the paired NAT samples, indicating that B7-H3 dysregulation may be important in the progression of bladder cancer. D.A. Spandidos 2015-03 2014-12-23 /pmc/articles/PMC4314980/ /pubmed/25663925 http://dx.doi.org/10.3892/ol.2014.2828 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
WU, DEYAO
ZHANG, ZICHUN
PAN, HUIXING
FAN, YUANFENG
QU, PING
ZHOU, JIAN
Upregulation of the B7/CD28 family member B7-H3 in bladder cancer
title Upregulation of the B7/CD28 family member B7-H3 in bladder cancer
title_full Upregulation of the B7/CD28 family member B7-H3 in bladder cancer
title_fullStr Upregulation of the B7/CD28 family member B7-H3 in bladder cancer
title_full_unstemmed Upregulation of the B7/CD28 family member B7-H3 in bladder cancer
title_short Upregulation of the B7/CD28 family member B7-H3 in bladder cancer
title_sort upregulation of the b7/cd28 family member b7-h3 in bladder cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314980/
https://www.ncbi.nlm.nih.gov/pubmed/25663925
http://dx.doi.org/10.3892/ol.2014.2828
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