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Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR

BACKGROUND: The aryl hydrocarbon receptor (AHR) repressor (AHRR), a member of growing superfamily, is a basic-helix-loop-helix/Per-AHR nuclear translocator (ARNT)-Sim (bHLH-PAS) protein. Recently, AHRR has been proposed to function as a putative new tumor suppressor gene based on some relevant studi...

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Autores principales: Li, Yuan-fang, Wang, Dan-dan, Zhao, Bai-wei, Wang, Wei, Yuan, Shu-qiang, Huang, Chun-yu, Chen, Yong-ming, Zheng, Yan, Keshari, Rajiv Prasad, Xia, Jian-chuan, Zhou, Zhi-wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428367/
https://www.ncbi.nlm.nih.gov/pubmed/22952704
http://dx.doi.org/10.1371/journal.pone.0043555
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author Li, Yuan-fang
Wang, Dan-dan
Zhao, Bai-wei
Wang, Wei
Yuan, Shu-qiang
Huang, Chun-yu
Chen, Yong-ming
Zheng, Yan
Keshari, Rajiv Prasad
Xia, Jian-chuan
Zhou, Zhi-wei
author_facet Li, Yuan-fang
Wang, Dan-dan
Zhao, Bai-wei
Wang, Wei
Yuan, Shu-qiang
Huang, Chun-yu
Chen, Yong-ming
Zheng, Yan
Keshari, Rajiv Prasad
Xia, Jian-chuan
Zhou, Zhi-wei
author_sort Li, Yuan-fang
collection PubMed
description BACKGROUND: The aryl hydrocarbon receptor (AHR) repressor (AHRR), a member of growing superfamily, is a basic-helix-loop-helix/Per-AHR nuclear translocator (ARNT)-Sim (bHLH-PAS) protein. Recently, AHRR has been proposed to function as a putative new tumor suppressor gene based on some relevant studies in multiple types of human cancers. This current study aims to investigate AHHR expression and its prognostic significance in primary gastric adenocarcinoma. METHODOLOGY/PRINCIPAL FINDINGS: The expression level of AHRR was analyzed using real-time quantitative PCR (RT-qPCR), western blotting, and immunohistochemical staining. It was clearly showed that the expression status of AHRR was reduced in tumor tissue samples compared with that in matched adjacent non-tumor tissue samples by RT-qPCR (P = 0.0423) and western blotting analysis (P = 0.004). Moreover, data revealed that AHRR without exon 8 (the active isoform) was the predominant form either in tumor tissues (66.7%, 8/12) or in matched adjacent non-tumor tissues (100.0%, 12/12), and the mRNA level of this isoform was significantly reduced in tumor tissues (P = 0.006). Immunohistochemistry analysis indicated that AHRR expression was significantly decreased in 175 of 410 (42.7%) gastric adenocarcinoma cases. Kaplan-Meier survival curves and Multivariate Cox analysis revealed that decreased expression of AHRR was significantly associated with poor prognosis in gastric adenocarcinoma patients. CONCLUSIONS/SIGNIFICANCE: Our data suggests that, in primary gastric adenocarcinoma, AHRR may play as a suppressor gene and its expression status has the potential to be an independent prognostic factor.
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spelling pubmed-34283672012-09-05 Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR Li, Yuan-fang Wang, Dan-dan Zhao, Bai-wei Wang, Wei Yuan, Shu-qiang Huang, Chun-yu Chen, Yong-ming Zheng, Yan Keshari, Rajiv Prasad Xia, Jian-chuan Zhou, Zhi-wei PLoS One Research Article BACKGROUND: The aryl hydrocarbon receptor (AHR) repressor (AHRR), a member of growing superfamily, is a basic-helix-loop-helix/Per-AHR nuclear translocator (ARNT)-Sim (bHLH-PAS) protein. Recently, AHRR has been proposed to function as a putative new tumor suppressor gene based on some relevant studies in multiple types of human cancers. This current study aims to investigate AHHR expression and its prognostic significance in primary gastric adenocarcinoma. METHODOLOGY/PRINCIPAL FINDINGS: The expression level of AHRR was analyzed using real-time quantitative PCR (RT-qPCR), western blotting, and immunohistochemical staining. It was clearly showed that the expression status of AHRR was reduced in tumor tissue samples compared with that in matched adjacent non-tumor tissue samples by RT-qPCR (P = 0.0423) and western blotting analysis (P = 0.004). Moreover, data revealed that AHRR without exon 8 (the active isoform) was the predominant form either in tumor tissues (66.7%, 8/12) or in matched adjacent non-tumor tissues (100.0%, 12/12), and the mRNA level of this isoform was significantly reduced in tumor tissues (P = 0.006). Immunohistochemistry analysis indicated that AHRR expression was significantly decreased in 175 of 410 (42.7%) gastric adenocarcinoma cases. Kaplan-Meier survival curves and Multivariate Cox analysis revealed that decreased expression of AHRR was significantly associated with poor prognosis in gastric adenocarcinoma patients. CONCLUSIONS/SIGNIFICANCE: Our data suggests that, in primary gastric adenocarcinoma, AHRR may play as a suppressor gene and its expression status has the potential to be an independent prognostic factor. Public Library of Science 2012-08-27 /pmc/articles/PMC3428367/ /pubmed/22952704 http://dx.doi.org/10.1371/journal.pone.0043555 Text en © 2012 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Yuan-fang
Wang, Dan-dan
Zhao, Bai-wei
Wang, Wei
Yuan, Shu-qiang
Huang, Chun-yu
Chen, Yong-ming
Zheng, Yan
Keshari, Rajiv Prasad
Xia, Jian-chuan
Zhou, Zhi-wei
Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR
title Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR
title_full Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR
title_fullStr Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR
title_full_unstemmed Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR
title_short Poor Prognosis of Gastric Adenocarcinoma with Decreased Expression of AHRR
title_sort poor prognosis of gastric adenocarcinoma with decreased expression of ahrr
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428367/
https://www.ncbi.nlm.nih.gov/pubmed/22952704
http://dx.doi.org/10.1371/journal.pone.0043555
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