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Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis

BACKGROUND: Gastric cancer is one of the most lethal tumors and is characterized by poor prognosis and lack of effective diagnostic or therapeutic biomarkers. The aim of this study was to find hub genes serving as biomarkers in gastric cancer diagnosis and therapy. METHODS: GSE66229 from Gene Expres...

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Detalles Bibliográficos
Autores principales: Li, Chunyang, Yu, Haopeng, Sun, Yajing, Zeng, Xiaoxi, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938783/
https://www.ncbi.nlm.nih.gov/pubmed/33717664
http://dx.doi.org/10.7717/peerj.10682
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author Li, Chunyang
Yu, Haopeng
Sun, Yajing
Zeng, Xiaoxi
Zhang, Wei
author_facet Li, Chunyang
Yu, Haopeng
Sun, Yajing
Zeng, Xiaoxi
Zhang, Wei
author_sort Li, Chunyang
collection PubMed
description BACKGROUND: Gastric cancer is one of the most lethal tumors and is characterized by poor prognosis and lack of effective diagnostic or therapeutic biomarkers. The aim of this study was to find hub genes serving as biomarkers in gastric cancer diagnosis and therapy. METHODS: GSE66229 from Gene Expression Omnibus (GEO) was used as training set. Genes bearing the top 25% standard deviations among all the samples in training set were performed to systematic weighted gene co-expression network analysis (WGCNA) to find candidate genes. Then, hub genes were further screened by using the “least absolute shrinkage and selection operator” (LASSO) logistic regression. Finally, hub genes were validated in the GSE54129 dataset from GEO by supervised learning method artificial neural network (ANN) algorithm. RESULTS: Twelve modules with strong preservation were identified by using WGCNA methods in training set. Of which, five modules significantly related to gastric cancer were selected as clinically significant modules, and 713 candidate genes were identified from these five modules. Then, ADIPOQ, ARHGAP39, ATAD3A, C1orf95, CWH43, GRIK3, INHBA, RDH12, SCNN1G, SIGLEC11 and LYVE1 were screened as the hub genes. These hub genes successfully differentiated the tumor samples from the healthy tissues in an independent testing set through artificial neural network algorithm with the area under the receiver operating characteristic curve at 0.946. CONCLUSIONS: These hub genes bearing diagnostic and therapeutic values, and our results may provide a novel prospect for the diagnosis and treatment of gastric cancer in the future.
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spelling pubmed-79387832021-03-12 Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis Li, Chunyang Yu, Haopeng Sun, Yajing Zeng, Xiaoxi Zhang, Wei PeerJ Bioinformatics BACKGROUND: Gastric cancer is one of the most lethal tumors and is characterized by poor prognosis and lack of effective diagnostic or therapeutic biomarkers. The aim of this study was to find hub genes serving as biomarkers in gastric cancer diagnosis and therapy. METHODS: GSE66229 from Gene Expression Omnibus (GEO) was used as training set. Genes bearing the top 25% standard deviations among all the samples in training set were performed to systematic weighted gene co-expression network analysis (WGCNA) to find candidate genes. Then, hub genes were further screened by using the “least absolute shrinkage and selection operator” (LASSO) logistic regression. Finally, hub genes were validated in the GSE54129 dataset from GEO by supervised learning method artificial neural network (ANN) algorithm. RESULTS: Twelve modules with strong preservation were identified by using WGCNA methods in training set. Of which, five modules significantly related to gastric cancer were selected as clinically significant modules, and 713 candidate genes were identified from these five modules. Then, ADIPOQ, ARHGAP39, ATAD3A, C1orf95, CWH43, GRIK3, INHBA, RDH12, SCNN1G, SIGLEC11 and LYVE1 were screened as the hub genes. These hub genes successfully differentiated the tumor samples from the healthy tissues in an independent testing set through artificial neural network algorithm with the area under the receiver operating characteristic curve at 0.946. CONCLUSIONS: These hub genes bearing diagnostic and therapeutic values, and our results may provide a novel prospect for the diagnosis and treatment of gastric cancer in the future. PeerJ Inc. 2021-03-05 /pmc/articles/PMC7938783/ /pubmed/33717664 http://dx.doi.org/10.7717/peerj.10682 Text en ©2021 Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Li, Chunyang
Yu, Haopeng
Sun, Yajing
Zeng, Xiaoxi
Zhang, Wei
Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
title Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
title_full Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
title_fullStr Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
title_full_unstemmed Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
title_short Identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
title_sort identification of the hub genes in gastric cancer through weighted gene co-expression network analysis
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938783/
https://www.ncbi.nlm.nih.gov/pubmed/33717664
http://dx.doi.org/10.7717/peerj.10682
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