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A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer

BACKGROUND: Previous study, using immunoblotting with IgG and membrane proteins, identified prohibitin (PHB) as a potential immunogenic membrane antigen. Now, investigate PHB expression and biological functions in pancreatic cancer. METHODS: PHB expression was analysed in PDAC cell lines, normal pan...

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Autores principales: Wang, Weibin, Xu, Lai, Yang, Yu, Dong, LiangBo, Zhao, BangBo, Lu, Jun, Zhang, Taiping, Zhao, Yupei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125288/
https://www.ncbi.nlm.nih.gov/pubmed/30185797
http://dx.doi.org/10.1038/s41424-018-0044-1
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author Wang, Weibin
Xu, Lai
Yang, Yu
Dong, LiangBo
Zhao, BangBo
Lu, Jun
Zhang, Taiping
Zhao, Yupei
author_facet Wang, Weibin
Xu, Lai
Yang, Yu
Dong, LiangBo
Zhao, BangBo
Lu, Jun
Zhang, Taiping
Zhao, Yupei
author_sort Wang, Weibin
collection PubMed
description BACKGROUND: Previous study, using immunoblotting with IgG and membrane proteins, identified prohibitin (PHB) as a potential immunogenic membrane antigen. Now, investigate PHB expression and biological functions in pancreatic cancer. METHODS: PHB expression was analysed in PDAC cell lines, normal pancreas tissues, cancer tissues, PDAC patient sera and healthy volunteer sera using QRT-PCR, Western blotting, IHC, and ELISA, and a survival analysis and a COX regression analysis were performed. Low and high PHB expression levels were accomplished using RNA interference technology and gene transfer techniques. Cell proliferation, migration, and invasion, apoptosis-related proteins were assessed 48 h after transfection. RESULTS: PHB was generally expressed in the 8 tested PDAC cell lines. PHB was significantly increased in PDAC tissues and negatively correlated with overall survival (p < 0.01). PHB was an independent prognostic factor in PDAC (p < 0.01). PHB was increased in PDAC patient sera (p < 0.01). siRNA-PHB decreased cell growth, migration and invasion. However, PHB overexpression resulted in the opposite effects. Western blotting and Flow cytometric analysis revealed apoptosis inhibition in siRNA-PHB PDAC cells. CONCLUSIONS: PHB plays a key role in modulating the malignant phenotype and apoptosis induction, which may be a novel prognostic predictor and a candidate for targeted therapy against PDAC.
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spelling pubmed-61252882018-09-06 A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer Wang, Weibin Xu, Lai Yang, Yu Dong, LiangBo Zhao, BangBo Lu, Jun Zhang, Taiping Zhao, Yupei Clin Transl Gastroenterol Article BACKGROUND: Previous study, using immunoblotting with IgG and membrane proteins, identified prohibitin (PHB) as a potential immunogenic membrane antigen. Now, investigate PHB expression and biological functions in pancreatic cancer. METHODS: PHB expression was analysed in PDAC cell lines, normal pancreas tissues, cancer tissues, PDAC patient sera and healthy volunteer sera using QRT-PCR, Western blotting, IHC, and ELISA, and a survival analysis and a COX regression analysis were performed. Low and high PHB expression levels were accomplished using RNA interference technology and gene transfer techniques. Cell proliferation, migration, and invasion, apoptosis-related proteins were assessed 48 h after transfection. RESULTS: PHB was generally expressed in the 8 tested PDAC cell lines. PHB was significantly increased in PDAC tissues and negatively correlated with overall survival (p < 0.01). PHB was an independent prognostic factor in PDAC (p < 0.01). PHB was increased in PDAC patient sera (p < 0.01). siRNA-PHB decreased cell growth, migration and invasion. However, PHB overexpression resulted in the opposite effects. Western blotting and Flow cytometric analysis revealed apoptosis inhibition in siRNA-PHB PDAC cells. CONCLUSIONS: PHB plays a key role in modulating the malignant phenotype and apoptosis induction, which may be a novel prognostic predictor and a candidate for targeted therapy against PDAC. Nature Publishing Group US 2018-09-06 /pmc/articles/PMC6125288/ /pubmed/30185797 http://dx.doi.org/10.1038/s41424-018-0044-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Weibin
Xu, Lai
Yang, Yu
Dong, LiangBo
Zhao, BangBo
Lu, Jun
Zhang, Taiping
Zhao, Yupei
A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer
title A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer
title_full A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer
title_fullStr A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer
title_full_unstemmed A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer
title_short A novel prognostic marker and immunogenic membrane antigen: prohibitin (PHB) in pancreatic cancer
title_sort novel prognostic marker and immunogenic membrane antigen: prohibitin (phb) in pancreatic cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125288/
https://www.ncbi.nlm.nih.gov/pubmed/30185797
http://dx.doi.org/10.1038/s41424-018-0044-1
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