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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
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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 |
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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 |
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