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Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis
Since the five-year survival rate is less than 5%, pancreatic ductal adenocarcinoma (PDAC) remains the 4th cause of cancer-related death. Although PDAC has been repeatedly researched in recent years, it is still predicted to be the second leading cause of cancer death by year 2030. In our study, the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821034/ https://www.ncbi.nlm.nih.gov/pubmed/29483831 http://dx.doi.org/10.7150/ijbs.22619 |
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author | Zhou, Zhou Cheng, Yian Jiang, Yinan Liu, Shi Zhang, Meng Liu, Jing Zhao, Qiu |
author_facet | Zhou, Zhou Cheng, Yian Jiang, Yinan Liu, Shi Zhang, Meng Liu, Jing Zhao, Qiu |
author_sort | Zhou, Zhou |
collection | PubMed |
description | Since the five-year survival rate is less than 5%, pancreatic ductal adenocarcinoma (PDAC) remains the 4th cause of cancer-related death. Although PDAC has been repeatedly researched in recent years, it is still predicted to be the second leading cause of cancer death by year 2030. In our study, the differentially expressed genes in dataset GSE62452 were used to construct a co-expression network by WGCNA. The yellow module related to grade of PDAC was screened. Combined with co-expression network and PPI network, 36 candidates were screened. After survival and regression analysis by using GSE62452 and TCGA dataset, we identified 10 real hub genes (CCNA2, CCNB1, CENPF, DLGAP5, KIF14, KIF23, NEK2, RACGAP1, TPX2 and UBE2C) tightly related to progression of PDAC. According to Oncomine database and The Human Protein Atlas (HPA), we found that all real hub genes were overexpressed in pancreatic carcinoma compared with normal tissues on transcriptional and translational level. ROC curve was plotted and AUC was calculated to distinguish recurrent and non-recurrent PDAC and every AUC of the real hub gene was greater than 0.5. Finally, functional enrichment analysis and gene set enrichment (GSEA) was performed and both of them showed the cell cycle played a vital role in PDAC. |
format | Online Article Text |
id | pubmed-5821034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-58210342018-02-26 Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis Zhou, Zhou Cheng, Yian Jiang, Yinan Liu, Shi Zhang, Meng Liu, Jing Zhao, Qiu Int J Biol Sci Research Paper Since the five-year survival rate is less than 5%, pancreatic ductal adenocarcinoma (PDAC) remains the 4th cause of cancer-related death. Although PDAC has been repeatedly researched in recent years, it is still predicted to be the second leading cause of cancer death by year 2030. In our study, the differentially expressed genes in dataset GSE62452 were used to construct a co-expression network by WGCNA. The yellow module related to grade of PDAC was screened. Combined with co-expression network and PPI network, 36 candidates were screened. After survival and regression analysis by using GSE62452 and TCGA dataset, we identified 10 real hub genes (CCNA2, CCNB1, CENPF, DLGAP5, KIF14, KIF23, NEK2, RACGAP1, TPX2 and UBE2C) tightly related to progression of PDAC. According to Oncomine database and The Human Protein Atlas (HPA), we found that all real hub genes were overexpressed in pancreatic carcinoma compared with normal tissues on transcriptional and translational level. ROC curve was plotted and AUC was calculated to distinguish recurrent and non-recurrent PDAC and every AUC of the real hub gene was greater than 0.5. Finally, functional enrichment analysis and gene set enrichment (GSEA) was performed and both of them showed the cell cycle played a vital role in PDAC. Ivyspring International Publisher 2018-01-12 /pmc/articles/PMC5821034/ /pubmed/29483831 http://dx.doi.org/10.7150/ijbs.22619 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Zhou, Zhou Cheng, Yian Jiang, Yinan Liu, Shi Zhang, Meng Liu, Jing Zhao, Qiu Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
title | Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
title_full | Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
title_fullStr | Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
title_full_unstemmed | Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
title_short | Ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
title_sort | ten hub genes associated with progression and prognosis of pancreatic carcinoma identified by co-expression analysis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821034/ https://www.ncbi.nlm.nih.gov/pubmed/29483831 http://dx.doi.org/10.7150/ijbs.22619 |
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