Cargando…

AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas

Pancreatic adenocarcinoma (PAAD) is a common and highly malignant tumor. The identification of prognostic biomarkers for PAAD could provide invaluable information for clinical treatment. AMP-activated protein kinase family member 5 (ARK5) is a member of the AMPK family that mediates the migration of...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Haokai, Mao, Jiayan, Yang, Xiaodan, Chen, Fei, Song, Zhengwei, Fei, Jianguo, Chen, Wei, Zhong, Zhengxiang, Wang, Xiaoguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533462/
https://www.ncbi.nlm.nih.gov/pubmed/33000197
http://dx.doi.org/10.3892/mmr.2020.11504
_version_ 1783590139575926784
author Xu, Haokai
Mao, Jiayan
Yang, Xiaodan
Chen, Fei
Song, Zhengwei
Fei, Jianguo
Chen, Wei
Zhong, Zhengxiang
Wang, Xiaoguang
author_facet Xu, Haokai
Mao, Jiayan
Yang, Xiaodan
Chen, Fei
Song, Zhengwei
Fei, Jianguo
Chen, Wei
Zhong, Zhengxiang
Wang, Xiaoguang
author_sort Xu, Haokai
collection PubMed
description Pancreatic adenocarcinoma (PAAD) is a common and highly malignant tumor. The identification of prognostic biomarkers for PAAD could provide invaluable information for clinical treatment. AMP-activated protein kinase family member 5 (ARK5) is a member of the AMPK family that mediates the migration of PAAD cells. In the present study, ARK5 expression was evaluated using bioinformatics analysis in public datasets from The Cancer Genome Atlas. The expression levels of ARK5 in PAAD tumor tissue were significantly increased, compared with matched non-cancerous tissues. ARK5 target genes were then predicted and Gene Ontology Biological Processes, Kyoto Encyclopedia of Genes and Genomes pathway analysis and Reactome gene sets were used to determine the functions associated with the target genes. A protein-protein interaction network was also constructed to find out the node genes and observe their association with the overall survival rate of PAAD. A total of nine node genes were identified in the PPI network, of which six were significantly upregulated in PAAD tissue, compared with matched normal tissue. The prognostic value of each node gene was evaluated by comparing the overall survival in patients with PAAD stratified according to the expression levels of these genes. Overall survival was significantly reduced in patients with high polo-like kinase-1 (PLK1) or protein phosphatase 1 catalytic subunit β (PPP1CB) expression, compared with patients with low expression of these genes. To further evaluate the relationship between PAAD and ARK5, ARK5 immunohistochemical staining was performed in a tissue microarray consisting of 112 tumor samples from patients with PAAD and adjacent normal tissue samples. ARK5 protein expression in PAAD tissue was markedly increased, compared with non-cancerous tissue (P=7.631×10(−11)). Moreover, ARK5 protein levels were associated with N stage (P=0.018). The overall survival of patients with PAAD with high ARK5 protein expression levels was reduced (P=0.014), compared with patients with low expression. In conclusion, these findings suggested that ARK5 may represent an independent prognostic indicator of PAAD.
format Online
Article
Text
id pubmed-7533462
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-75334622020-10-07 AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas Xu, Haokai Mao, Jiayan Yang, Xiaodan Chen, Fei Song, Zhengwei Fei, Jianguo Chen, Wei Zhong, Zhengxiang Wang, Xiaoguang Mol Med Rep Articles Pancreatic adenocarcinoma (PAAD) is a common and highly malignant tumor. The identification of prognostic biomarkers for PAAD could provide invaluable information for clinical treatment. AMP-activated protein kinase family member 5 (ARK5) is a member of the AMPK family that mediates the migration of PAAD cells. In the present study, ARK5 expression was evaluated using bioinformatics analysis in public datasets from The Cancer Genome Atlas. The expression levels of ARK5 in PAAD tumor tissue were significantly increased, compared with matched non-cancerous tissues. ARK5 target genes were then predicted and Gene Ontology Biological Processes, Kyoto Encyclopedia of Genes and Genomes pathway analysis and Reactome gene sets were used to determine the functions associated with the target genes. A protein-protein interaction network was also constructed to find out the node genes and observe their association with the overall survival rate of PAAD. A total of nine node genes were identified in the PPI network, of which six were significantly upregulated in PAAD tissue, compared with matched normal tissue. The prognostic value of each node gene was evaluated by comparing the overall survival in patients with PAAD stratified according to the expression levels of these genes. Overall survival was significantly reduced in patients with high polo-like kinase-1 (PLK1) or protein phosphatase 1 catalytic subunit β (PPP1CB) expression, compared with patients with low expression of these genes. To further evaluate the relationship between PAAD and ARK5, ARK5 immunohistochemical staining was performed in a tissue microarray consisting of 112 tumor samples from patients with PAAD and adjacent normal tissue samples. ARK5 protein expression in PAAD tissue was markedly increased, compared with non-cancerous tissue (P=7.631×10(−11)). Moreover, ARK5 protein levels were associated with N stage (P=0.018). The overall survival of patients with PAAD with high ARK5 protein expression levels was reduced (P=0.014), compared with patients with low expression. In conclusion, these findings suggested that ARK5 may represent an independent prognostic indicator of PAAD. D.A. Spandidos 2020-11 2020-09-10 /pmc/articles/PMC7533462/ /pubmed/33000197 http://dx.doi.org/10.3892/mmr.2020.11504 Text en Copyright: © Xu 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
Xu, Haokai
Mao, Jiayan
Yang, Xiaodan
Chen, Fei
Song, Zhengwei
Fei, Jianguo
Chen, Wei
Zhong, Zhengxiang
Wang, Xiaoguang
AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas
title AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas
title_full AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas
title_fullStr AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas
title_full_unstemmed AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas
title_short AMP-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: A study based on The Cancer Genome Atlas
title_sort amp-activated protein kinase family member 5 is an independent prognostic indicator of pancreatic adenocarcinoma: a study based on the cancer genome atlas
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533462/
https://www.ncbi.nlm.nih.gov/pubmed/33000197
http://dx.doi.org/10.3892/mmr.2020.11504
work_keys_str_mv AT xuhaokai ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT maojiayan ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT yangxiaodan ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT chenfei ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT songzhengwei ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT feijianguo ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT chenwei ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT zhongzhengxiang ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas
AT wangxiaoguang ampactivatedproteinkinasefamilymember5isanindependentprognosticindicatorofpancreaticadenocarcinomaastudybasedonthecancergenomeatlas