Cargando…

Gene expression profiling analysis of lung adenocarcinoma

The present study screened potential genes related to lung adenocarcinoma, with the aim of further understanding disease pathogenesis. The GSE2514 dataset including 20 lung adenocarcinoma and 19 adjacent normal tissue samples from 10 patients with lung adenocarcinoma aged 45-73 years was downloaded...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, H., Ma, J., Wu, J., Chen, L., Sun, F., Qu, C., Zheng, D., Xu, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763816/
https://www.ncbi.nlm.nih.gov/pubmed/26840709
http://dx.doi.org/10.1590/1414-431X20154861
_version_ 1782417321408593920
author Xu, H.
Ma, J.
Wu, J.
Chen, L.
Sun, F.
Qu, C.
Zheng, D.
Xu, S.
author_facet Xu, H.
Ma, J.
Wu, J.
Chen, L.
Sun, F.
Qu, C.
Zheng, D.
Xu, S.
author_sort Xu, H.
collection PubMed
description The present study screened potential genes related to lung adenocarcinoma, with the aim of further understanding disease pathogenesis. The GSE2514 dataset including 20 lung adenocarcinoma and 19 adjacent normal tissue samples from 10 patients with lung adenocarcinoma aged 45-73 years was downloaded from Gene Expression Omnibus. Differentially expressed genes (DEGs) between the two groups were screened using the t-test. Potential gene functions were predicted using functional and pathway enrichment analysis, and protein-protein interaction (PPI) networks obtained from the STRING database were constructed with Cytoscape. Module analysis of PPI networks was performed through MCODE in Cytoscape. In total, 535 upregulated and 465 downregulated DEGs were identified. These included ATP5D, UQCRC2, UQCR11 and genes encoding nicotinamide adenine dinucleotide (NADH), which are mainly associated with mitochondrial ATP synthesis coupled electron transport, and which were enriched in the oxidative phosphorylation pathway. Other DEGs were associated with DNA replication (PRIM1, MCM3, and RNASEH2A), cell surface receptor-linked signal transduction and the enzyme-linked receptor protein signaling pathway (MAPK1, STAT3, RAF1, and JAK1), and regulation of the cytoskeleton and phosphatidylinositol signaling system (PIP5K1B, PIP5K1C, and PIP4K2B). Our findings suggest that DEGs encoding subunits of NADH, PRIM1, MCM3, MAPK1, STAT3, RAF1, and JAK1 might be associated with the development of lung adenocarcinoma.
format Online
Article
Text
id pubmed-4763816
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Associação Brasileira de Divulgação Científica
record_format MEDLINE/PubMed
spelling pubmed-47638162016-03-07 Gene expression profiling analysis of lung adenocarcinoma Xu, H. Ma, J. Wu, J. Chen, L. Sun, F. Qu, C. Zheng, D. Xu, S. Braz J Med Biol Res Biomedical Sciences The present study screened potential genes related to lung adenocarcinoma, with the aim of further understanding disease pathogenesis. The GSE2514 dataset including 20 lung adenocarcinoma and 19 adjacent normal tissue samples from 10 patients with lung adenocarcinoma aged 45-73 years was downloaded from Gene Expression Omnibus. Differentially expressed genes (DEGs) between the two groups were screened using the t-test. Potential gene functions were predicted using functional and pathway enrichment analysis, and protein-protein interaction (PPI) networks obtained from the STRING database were constructed with Cytoscape. Module analysis of PPI networks was performed through MCODE in Cytoscape. In total, 535 upregulated and 465 downregulated DEGs were identified. These included ATP5D, UQCRC2, UQCR11 and genes encoding nicotinamide adenine dinucleotide (NADH), which are mainly associated with mitochondrial ATP synthesis coupled electron transport, and which were enriched in the oxidative phosphorylation pathway. Other DEGs were associated with DNA replication (PRIM1, MCM3, and RNASEH2A), cell surface receptor-linked signal transduction and the enzyme-linked receptor protein signaling pathway (MAPK1, STAT3, RAF1, and JAK1), and regulation of the cytoskeleton and phosphatidylinositol signaling system (PIP5K1B, PIP5K1C, and PIP4K2B). Our findings suggest that DEGs encoding subunits of NADH, PRIM1, MCM3, MAPK1, STAT3, RAF1, and JAK1 might be associated with the development of lung adenocarcinoma. Associação Brasileira de Divulgação Científica 2016-02-02 /pmc/articles/PMC4763816/ /pubmed/26840709 http://dx.doi.org/10.1590/1414-431X20154861 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biomedical Sciences
Xu, H.
Ma, J.
Wu, J.
Chen, L.
Sun, F.
Qu, C.
Zheng, D.
Xu, S.
Gene expression profiling analysis of lung adenocarcinoma
title Gene expression profiling analysis of lung adenocarcinoma
title_full Gene expression profiling analysis of lung adenocarcinoma
title_fullStr Gene expression profiling analysis of lung adenocarcinoma
title_full_unstemmed Gene expression profiling analysis of lung adenocarcinoma
title_short Gene expression profiling analysis of lung adenocarcinoma
title_sort gene expression profiling analysis of lung adenocarcinoma
topic Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763816/
https://www.ncbi.nlm.nih.gov/pubmed/26840709
http://dx.doi.org/10.1590/1414-431X20154861
work_keys_str_mv AT xuh geneexpressionprofilinganalysisoflungadenocarcinoma
AT maj geneexpressionprofilinganalysisoflungadenocarcinoma
AT wuj geneexpressionprofilinganalysisoflungadenocarcinoma
AT chenl geneexpressionprofilinganalysisoflungadenocarcinoma
AT sunf geneexpressionprofilinganalysisoflungadenocarcinoma
AT quc geneexpressionprofilinganalysisoflungadenocarcinoma
AT zhengd geneexpressionprofilinganalysisoflungadenocarcinoma
AT xus geneexpressionprofilinganalysisoflungadenocarcinoma