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Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method

Postmenopausal osteoporosis (PO) imposes great burden on individuals and society. This study predicted hub genes and gene functions for PO by an integration of the convergent evidence (CE) method, rank product (RP) algorithm and the combing of P-values. Using the gene expression data, genes were ran...

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Autores principales: Cao, Honghai, Zhang, Lihai, Chen, Hua, Zhang, Wei, Zhang, Qun, Liang, Xiangdang, Guo, Yizhu, Tang, Peifu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327640/
https://www.ncbi.nlm.nih.gov/pubmed/30680001
http://dx.doi.org/10.3892/etm.2018.7095
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author Cao, Honghai
Zhang, Lihai
Chen, Hua
Zhang, Wei
Zhang, Qun
Liang, Xiangdang
Guo, Yizhu
Tang, Peifu
author_facet Cao, Honghai
Zhang, Lihai
Chen, Hua
Zhang, Wei
Zhang, Qun
Liang, Xiangdang
Guo, Yizhu
Tang, Peifu
author_sort Cao, Honghai
collection PubMed
description Postmenopausal osteoporosis (PO) imposes great burden on individuals and society. This study predicted hub genes and gene functions for PO by an integration of the convergent evidence (CE) method, rank product (RP) algorithm and the combing of P-values. Using the gene expression data, genes were ranked by the CE method, RP algorithm and combing P-values, respectively. Subsequently, the top 100 genes were selected from each of the three gene lists, and then the common genes for two or three methods were denoted as informative genes of PO. A mutual information network (MIN) was constructed for the informative genes utilizing the context likelihood of relatedness algorithm. Topological centrality (degree) analysis was conducted on the MIN to investigate hub genes. Then we performed Gene Ontology (GO) enrichment analysis dependent upon the Biological Networks Gene Ontology tool (BiNGO) plugin of Cytoscape to investigate hub gene functions for PO patients. Consequently, a total of 82 informative genes were obtained by integrating the results of the three methods. There were 82 nodes and 1,741 edges in the MIN, of which 8 hub genes were identified, such as PFN1, EEF2 and S100A9. The result of GO enrichment analysis showed that 49 GO terms with P<0.001 were detected, especially the top 5 gene sets were defined as hub gene functions of PO, for instance, translational elongation, translation and cellular macromolecule biosynthetic process. In conclusion, we have predicted 8 hub genes and 5 hub gene functions associated with PO patients. The findings might help understand the molecular mechanism underlying PO.
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spelling pubmed-63276402019-01-24 Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method Cao, Honghai Zhang, Lihai Chen, Hua Zhang, Wei Zhang, Qun Liang, Xiangdang Guo, Yizhu Tang, Peifu Exp Ther Med Articles Postmenopausal osteoporosis (PO) imposes great burden on individuals and society. This study predicted hub genes and gene functions for PO by an integration of the convergent evidence (CE) method, rank product (RP) algorithm and the combing of P-values. Using the gene expression data, genes were ranked by the CE method, RP algorithm and combing P-values, respectively. Subsequently, the top 100 genes were selected from each of the three gene lists, and then the common genes for two or three methods were denoted as informative genes of PO. A mutual information network (MIN) was constructed for the informative genes utilizing the context likelihood of relatedness algorithm. Topological centrality (degree) analysis was conducted on the MIN to investigate hub genes. Then we performed Gene Ontology (GO) enrichment analysis dependent upon the Biological Networks Gene Ontology tool (BiNGO) plugin of Cytoscape to investigate hub gene functions for PO patients. Consequently, a total of 82 informative genes were obtained by integrating the results of the three methods. There were 82 nodes and 1,741 edges in the MIN, of which 8 hub genes were identified, such as PFN1, EEF2 and S100A9. The result of GO enrichment analysis showed that 49 GO terms with P<0.001 were detected, especially the top 5 gene sets were defined as hub gene functions of PO, for instance, translational elongation, translation and cellular macromolecule biosynthetic process. In conclusion, we have predicted 8 hub genes and 5 hub gene functions associated with PO patients. The findings might help understand the molecular mechanism underlying PO. D.A. Spandidos 2019-02 2018-12-13 /pmc/articles/PMC6327640/ /pubmed/30680001 http://dx.doi.org/10.3892/etm.2018.7095 Text en Copyright: © Cao 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
Cao, Honghai
Zhang, Lihai
Chen, Hua
Zhang, Wei
Zhang, Qun
Liang, Xiangdang
Guo, Yizhu
Tang, Peifu
Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
title Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
title_full Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
title_fullStr Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
title_full_unstemmed Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
title_short Hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
title_sort hub genes and gene functions associated with postmenopausal osteoporosis predicted by an integrated method
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327640/
https://www.ncbi.nlm.nih.gov/pubmed/30680001
http://dx.doi.org/10.3892/etm.2018.7095
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