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Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA

Hepatocellular carcinoma (HCC) is a devastating disease worldwide. Though many efforts have been made to elucidate the process of HCC, its molecular mechanisms of development remain elusive due to its complexity. To explore the stepwise carcinogenic process from pre-neoplastic lesions to the end sta...

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Autores principales: Yin, Li, Cai, Zhihui, Zhu, Baoan, Xu, Cunshuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852588/
https://www.ncbi.nlm.nih.gov/pubmed/29443924
http://dx.doi.org/10.3390/genes9020092
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author Yin, Li
Cai, Zhihui
Zhu, Baoan
Xu, Cunshuan
author_facet Yin, Li
Cai, Zhihui
Zhu, Baoan
Xu, Cunshuan
author_sort Yin, Li
collection PubMed
description Hepatocellular carcinoma (HCC) is a devastating disease worldwide. Though many efforts have been made to elucidate the process of HCC, its molecular mechanisms of development remain elusive due to its complexity. To explore the stepwise carcinogenic process from pre-neoplastic lesions to the end stage of HCC, we employed weighted gene co-expression network analysis (WGCNA) which has been proved to be an effective method in many diseases to detect co-expressed modules and hub genes using eight pathological stages including normal, cirrhosis without HCC, cirrhosis, low-grade dysplastic, high-grade dysplastic, very early and early, advanced HCC and very advanced HCC. Among the eight consecutive pathological stages, five representative modules are selected to perform canonical pathway enrichment and upstream regulator analysis by using ingenuity pathway analysis (IPA) software. We found that cell cycle related biological processes were activated at four neoplastic stages, and the degree of activation of the cell cycle corresponded to the deterioration degree of HCC. The orange and yellow modules enriched in energy metabolism, especially oxidative metabolism, and the expression value of the genes decreased only at four neoplastic stages. The brown module, enriched in protein ubiquitination and ephrin receptor signaling pathways, correlated mainly with the very early stage of HCC. The darkred module, enriched in hepatic fibrosis/hepatic stellate cell activation, correlated with the cirrhotic stage only. The high degree hub genes were identified based on the protein-protein interaction (PPI) network and were verified by Kaplan-Meier survival analysis. The novel five high degree hub genes signature that was identified in our study may shed light on future prognostic and therapeutic approaches. Our study brings a new perspective to the understanding of the key pathways and genes in the dynamic changes of HCC progression. These findings shed light on further investigations.
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spelling pubmed-58525882018-03-19 Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA Yin, Li Cai, Zhihui Zhu, Baoan Xu, Cunshuan Genes (Basel) Article Hepatocellular carcinoma (HCC) is a devastating disease worldwide. Though many efforts have been made to elucidate the process of HCC, its molecular mechanisms of development remain elusive due to its complexity. To explore the stepwise carcinogenic process from pre-neoplastic lesions to the end stage of HCC, we employed weighted gene co-expression network analysis (WGCNA) which has been proved to be an effective method in many diseases to detect co-expressed modules and hub genes using eight pathological stages including normal, cirrhosis without HCC, cirrhosis, low-grade dysplastic, high-grade dysplastic, very early and early, advanced HCC and very advanced HCC. Among the eight consecutive pathological stages, five representative modules are selected to perform canonical pathway enrichment and upstream regulator analysis by using ingenuity pathway analysis (IPA) software. We found that cell cycle related biological processes were activated at four neoplastic stages, and the degree of activation of the cell cycle corresponded to the deterioration degree of HCC. The orange and yellow modules enriched in energy metabolism, especially oxidative metabolism, and the expression value of the genes decreased only at four neoplastic stages. The brown module, enriched in protein ubiquitination and ephrin receptor signaling pathways, correlated mainly with the very early stage of HCC. The darkred module, enriched in hepatic fibrosis/hepatic stellate cell activation, correlated with the cirrhotic stage only. The high degree hub genes were identified based on the protein-protein interaction (PPI) network and were verified by Kaplan-Meier survival analysis. The novel five high degree hub genes signature that was identified in our study may shed light on future prognostic and therapeutic approaches. Our study brings a new perspective to the understanding of the key pathways and genes in the dynamic changes of HCC progression. These findings shed light on further investigations. MDPI 2018-02-14 /pmc/articles/PMC5852588/ /pubmed/29443924 http://dx.doi.org/10.3390/genes9020092 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yin, Li
Cai, Zhihui
Zhu, Baoan
Xu, Cunshuan
Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA
title Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA
title_full Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA
title_fullStr Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA
title_full_unstemmed Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA
title_short Identification of Key Pathways and Genes in the Dynamic Progression of HCC Based on WGCNA
title_sort identification of key pathways and genes in the dynamic progression of hcc based on wgcna
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852588/
https://www.ncbi.nlm.nih.gov/pubmed/29443924
http://dx.doi.org/10.3390/genes9020092
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