Cargando…

Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining

The purpose of this study was to describe breast atypical hyperplasia (BAH)-related gene expression and to systematically analyze the functions, pathways, and networks of BAH-related hub genes. On the basis of natural language processing, gene data for BAH were extracted from the PubMed database usi...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Wei, Shi, Bei, Zhao, Fangkun, Wu, Yunfei, Jin, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784767/
https://www.ncbi.nlm.nih.gov/pubmed/30394935
http://dx.doi.org/10.1097/CEJ.0000000000000494
_version_ 1783457804454985728
author Ma, Wei
Shi, Bei
Zhao, Fangkun
Wu, Yunfei
Jin, Feng
author_facet Ma, Wei
Shi, Bei
Zhao, Fangkun
Wu, Yunfei
Jin, Feng
author_sort Ma, Wei
collection PubMed
description The purpose of this study was to describe breast atypical hyperplasia (BAH)-related gene expression and to systematically analyze the functions, pathways, and networks of BAH-related hub genes. On the basis of natural language processing, gene data for BAH were extracted from the PubMed database using text mining. The enriched Gene Ontology terms and Kyoto Encyclopedia of Genes and Genomes pathways were obtained using DAVID (http://david.abcc.ncifcrf.gov/). A protein–protein interaction network was constructed using the STRING database. Hub genes were identified as genes that interact with at least 10 other genes within the BAH-related gene network. In total, 138 BAH-associated genes were identified as significant (P < 0.05), and 133 pathways were identified as significant (P < 0.05, false discovery rate < 0.05). A BAH-related protein network that included 81 interactions was constructed. Twenty genes were determined to interact with at least 10 others (P < 0.05, false discovery rate < 0.05) and were identified as the BAH-related hub genes of this protein–protein interaction network. These 20 genes are TP53, PIK3CA, JUN, MYC, EGFR, CCND1, AKT1, ERBB2, CTNN1B, ESR1, IGF-1, VEGFA, HRAS, CDKN1B, CDKN1A, PCNA, HGF, HIF1A, RB1, and STAT5A. This study may help to disclose the molecular mechanisms of BAH development and provide implications for BAH-targeted therapy or even breast cancer prevention. Nevertheless, connections between certain genes and BAH require further exploration.
format Online
Article
Text
id pubmed-6784767
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-67847672019-11-18 Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining Ma, Wei Shi, Bei Zhao, Fangkun Wu, Yunfei Jin, Feng Eur J Cancer Prev Research Papers: Breast Cancer The purpose of this study was to describe breast atypical hyperplasia (BAH)-related gene expression and to systematically analyze the functions, pathways, and networks of BAH-related hub genes. On the basis of natural language processing, gene data for BAH were extracted from the PubMed database using text mining. The enriched Gene Ontology terms and Kyoto Encyclopedia of Genes and Genomes pathways were obtained using DAVID (http://david.abcc.ncifcrf.gov/). A protein–protein interaction network was constructed using the STRING database. Hub genes were identified as genes that interact with at least 10 other genes within the BAH-related gene network. In total, 138 BAH-associated genes were identified as significant (P < 0.05), and 133 pathways were identified as significant (P < 0.05, false discovery rate < 0.05). A BAH-related protein network that included 81 interactions was constructed. Twenty genes were determined to interact with at least 10 others (P < 0.05, false discovery rate < 0.05) and were identified as the BAH-related hub genes of this protein–protein interaction network. These 20 genes are TP53, PIK3CA, JUN, MYC, EGFR, CCND1, AKT1, ERBB2, CTNN1B, ESR1, IGF-1, VEGFA, HRAS, CDKN1B, CDKN1A, PCNA, HGF, HIF1A, RB1, and STAT5A. This study may help to disclose the molecular mechanisms of BAH development and provide implications for BAH-targeted therapy or even breast cancer prevention. Nevertheless, connections between certain genes and BAH require further exploration. Lippincott Williams & Wilkins 2019-11 2018-11-07 /pmc/articles/PMC6784767/ /pubmed/30394935 http://dx.doi.org/10.1097/CEJ.0000000000000494 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Research Papers: Breast Cancer
Ma, Wei
Shi, Bei
Zhao, Fangkun
Wu, Yunfei
Jin, Feng
Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
title Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
title_full Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
title_fullStr Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
title_full_unstemmed Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
title_short Systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
title_sort systematic analysis of breast atypical hyperplasia-associated hub genes and pathways based on text mining
topic Research Papers: Breast Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784767/
https://www.ncbi.nlm.nih.gov/pubmed/30394935
http://dx.doi.org/10.1097/CEJ.0000000000000494
work_keys_str_mv AT mawei systematicanalysisofbreastatypicalhyperplasiaassociatedhubgenesandpathwaysbasedontextmining
AT shibei systematicanalysisofbreastatypicalhyperplasiaassociatedhubgenesandpathwaysbasedontextmining
AT zhaofangkun systematicanalysisofbreastatypicalhyperplasiaassociatedhubgenesandpathwaysbasedontextmining
AT wuyunfei systematicanalysisofbreastatypicalhyperplasiaassociatedhubgenesandpathwaysbasedontextmining
AT jinfeng systematicanalysisofbreastatypicalhyperplasiaassociatedhubgenesandpathwaysbasedontextmining