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Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles

Gene expression data of hepatocellular carcinoma (HCC) was compared with that of cirrhosis (C) to identify critical genes in HCC. A total of five gene expression data sets were downloaded from Gene Expression Omnibus. HCC and healthy samples were combined as dataset HCC, whereas cirrhosis samples we...

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Autores principales: Jiang, Mingming, Zeng, Qingfang, Dai, Suiping, Liang, Huixia, Dai, Fengying, Xie, Xueling, Lu, Kunlin, Gao, Chunfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355740/
https://www.ncbi.nlm.nih.gov/pubmed/27959423
http://dx.doi.org/10.3892/mmr.2016.6021
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author Jiang, Mingming
Zeng, Qingfang
Dai, Suiping
Liang, Huixia
Dai, Fengying
Xie, Xueling
Lu, Kunlin
Gao, Chunfang
author_facet Jiang, Mingming
Zeng, Qingfang
Dai, Suiping
Liang, Huixia
Dai, Fengying
Xie, Xueling
Lu, Kunlin
Gao, Chunfang
author_sort Jiang, Mingming
collection PubMed
description Gene expression data of hepatocellular carcinoma (HCC) was compared with that of cirrhosis (C) to identify critical genes in HCC. A total of five gene expression data sets were downloaded from Gene Expression Omnibus. HCC and healthy samples were combined as dataset HCC, whereas cirrhosis samples were included in dataset C. A network was constructed for dataset HCC with the package R for performing Weighted Gene Co-expression Network Analysis. Modules were identified by cluster analysis with the packages flashClust and dynamicTreeCut. Hub genes were screened out by calculating connectivity. Functional annotations were assigned to the hub genes using the Database for Annotation, Visualization and Integration Discovery, and functional annotation networks were visualized with Cytoscape. Following the exclusion of outlier samples, 394 HCC samples and 47 healthy samples were included in dataset HCC and 233 cirrhosis samples were included in dataset C. A total of 6 modules were identified in the weighted gene co-expression network of dataset HCC (blue, brown, turquoise, green, red and yellow). Modules blue, brown and turquoise had high preservation whereas module yellow exhibited the lowest preservation. These modules were associated with transcription, mitosis, cation transportation, cation homeostasis, secretion and regulation of cyclase activity. Various hub genes of module yellow were cytokines, including chemokine (C-C motif) ligand 22 and interleukin-19, which may be important in the development of HCC. Gene expression profiles of HCC were compared with those of cirrhosis and numerous critical genes were identified, which may contribute to the progression of HCC. Further studies on these genes may improve the understanding of HCC pathogenesis.
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spelling pubmed-53557402017-03-31 Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles Jiang, Mingming Zeng, Qingfang Dai, Suiping Liang, Huixia Dai, Fengying Xie, Xueling Lu, Kunlin Gao, Chunfang Mol Med Rep Articles Gene expression data of hepatocellular carcinoma (HCC) was compared with that of cirrhosis (C) to identify critical genes in HCC. A total of five gene expression data sets were downloaded from Gene Expression Omnibus. HCC and healthy samples were combined as dataset HCC, whereas cirrhosis samples were included in dataset C. A network was constructed for dataset HCC with the package R for performing Weighted Gene Co-expression Network Analysis. Modules were identified by cluster analysis with the packages flashClust and dynamicTreeCut. Hub genes were screened out by calculating connectivity. Functional annotations were assigned to the hub genes using the Database for Annotation, Visualization and Integration Discovery, and functional annotation networks were visualized with Cytoscape. Following the exclusion of outlier samples, 394 HCC samples and 47 healthy samples were included in dataset HCC and 233 cirrhosis samples were included in dataset C. A total of 6 modules were identified in the weighted gene co-expression network of dataset HCC (blue, brown, turquoise, green, red and yellow). Modules blue, brown and turquoise had high preservation whereas module yellow exhibited the lowest preservation. These modules were associated with transcription, mitosis, cation transportation, cation homeostasis, secretion and regulation of cyclase activity. Various hub genes of module yellow were cytokines, including chemokine (C-C motif) ligand 22 and interleukin-19, which may be important in the development of HCC. Gene expression profiles of HCC were compared with those of cirrhosis and numerous critical genes were identified, which may contribute to the progression of HCC. Further studies on these genes may improve the understanding of HCC pathogenesis. D.A. Spandidos 2017-01 2016-12-09 /pmc/articles/PMC5355740/ /pubmed/27959423 http://dx.doi.org/10.3892/mmr.2016.6021 Text en Copyright: © Jiang 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
Jiang, Mingming
Zeng, Qingfang
Dai, Suiping
Liang, Huixia
Dai, Fengying
Xie, Xueling
Lu, Kunlin
Gao, Chunfang
Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
title Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
title_full Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
title_fullStr Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
title_full_unstemmed Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
title_short Comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
title_sort comparative analysis of hepatocellular carcinoma and cirrhosis gene expression profiles
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355740/
https://www.ncbi.nlm.nih.gov/pubmed/27959423
http://dx.doi.org/10.3892/mmr.2016.6021
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