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Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA

Pancreatic adenocarcinoma is one of the leading causes of cancer-related death worldwide. Since little clinical symptoms were shown in the early period of pancreatic adenocarcinoma, most patients were found to carry metastases when diagnosis. The lack of effective diagnosis biomarkers and therapeuti...

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Autores principales: Huang, Liya, Ye, Ting, Wang, Jingjing, Gu, Xiaojing, Ma, Ruiting, Sheng, Lulu, Ma, Binwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762281/
https://www.ncbi.nlm.nih.gov/pubmed/35047023
http://dx.doi.org/10.3389/fgene.2021.814798
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author Huang, Liya
Ye, Ting
Wang, Jingjing
Gu, Xiaojing
Ma, Ruiting
Sheng, Lulu
Ma, Binwu
author_facet Huang, Liya
Ye, Ting
Wang, Jingjing
Gu, Xiaojing
Ma, Ruiting
Sheng, Lulu
Ma, Binwu
author_sort Huang, Liya
collection PubMed
description Pancreatic adenocarcinoma is one of the leading causes of cancer-related death worldwide. Since little clinical symptoms were shown in the early period of pancreatic adenocarcinoma, most patients were found to carry metastases when diagnosis. The lack of effective diagnosis biomarkers and therapeutic targets makes pancreatic adenocarcinoma difficult to screen and cure. The fundamental problem is we know very little about the regulatory mechanisms during carcinogenesis. Here, we employed weighted gene co-expression network analysis (WGCNA) to build gene interaction network using expression profile of pancreatic adenocarcinoma from The Cancer Genome Atlas (TCGA). STRING was used for the construction and visualization of biological networks. A total of 22 modules were detected in the network, among which yellow and pink modules showed the most significant associations with pancreatic adenocarcinoma. Dozens of new genes including PKMYT1, WDHD1, ASF1B, and RAD18 were identified. Further survival analysis yielded their valuable effects on the diagnosis and treatment of pancreatic adenocarcinoma. Our study pioneered network-based algorithm in the application of tumor etiology and discovered several promising regulators for pancreatic adenocarcinoma detection and therapy.
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spelling pubmed-87622812022-01-18 Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA Huang, Liya Ye, Ting Wang, Jingjing Gu, Xiaojing Ma, Ruiting Sheng, Lulu Ma, Binwu Front Genet Genetics Pancreatic adenocarcinoma is one of the leading causes of cancer-related death worldwide. Since little clinical symptoms were shown in the early period of pancreatic adenocarcinoma, most patients were found to carry metastases when diagnosis. The lack of effective diagnosis biomarkers and therapeutic targets makes pancreatic adenocarcinoma difficult to screen and cure. The fundamental problem is we know very little about the regulatory mechanisms during carcinogenesis. Here, we employed weighted gene co-expression network analysis (WGCNA) to build gene interaction network using expression profile of pancreatic adenocarcinoma from The Cancer Genome Atlas (TCGA). STRING was used for the construction and visualization of biological networks. A total of 22 modules were detected in the network, among which yellow and pink modules showed the most significant associations with pancreatic adenocarcinoma. Dozens of new genes including PKMYT1, WDHD1, ASF1B, and RAD18 were identified. Further survival analysis yielded their valuable effects on the diagnosis and treatment of pancreatic adenocarcinoma. Our study pioneered network-based algorithm in the application of tumor etiology and discovered several promising regulators for pancreatic adenocarcinoma detection and therapy. Frontiers Media S.A. 2022-01-03 /pmc/articles/PMC8762281/ /pubmed/35047023 http://dx.doi.org/10.3389/fgene.2021.814798 Text en Copyright © 2022 Huang, Ye, Wang, Gu, Ma, Sheng and Ma. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Huang, Liya
Ye, Ting
Wang, Jingjing
Gu, Xiaojing
Ma, Ruiting
Sheng, Lulu
Ma, Binwu
Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA
title Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA
title_full Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA
title_fullStr Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA
title_full_unstemmed Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA
title_short Identification of Survival-Associated Hub Genes in Pancreatic Adenocarcinoma Based on WGCNA
title_sort identification of survival-associated hub genes in pancreatic adenocarcinoma based on wgcna
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762281/
https://www.ncbi.nlm.nih.gov/pubmed/35047023
http://dx.doi.org/10.3389/fgene.2021.814798
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