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Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network

Background: Breast cancer is the second largest cancer in the world, the incidence of breast cancer continues to rise worldwide, and women’s health is seriously threatened. Therefore, it is very important to explore the characteristic changes of breast cancer from the gene level, including the scree...

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Autores principales: Zhang, Shumei, Jiang, Haoran, Gao, Bo, Yang, Wen, Wang, Guohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790293/
https://www.ncbi.nlm.nih.gov/pubmed/35096840
http://dx.doi.org/10.3389/fcell.2021.811585
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author Zhang, Shumei
Jiang, Haoran
Gao, Bo
Yang, Wen
Wang, Guohua
author_facet Zhang, Shumei
Jiang, Haoran
Gao, Bo
Yang, Wen
Wang, Guohua
author_sort Zhang, Shumei
collection PubMed
description Background: Breast cancer is the second largest cancer in the world, the incidence of breast cancer continues to rise worldwide, and women’s health is seriously threatened. Therefore, it is very important to explore the characteristic changes of breast cancer from the gene level, including the screening of differentially expressed genes and the identification of diagnostic markers. Methods: The gene expression profiles of breast cancer were obtained from the TCGA database. The edgeR R software package was used to screen the differentially expressed genes between breast cancer patients and normal samples. The function and pathway enrichment analysis of these genes revealed significant enrichment of functions and pathways. Next, download these pathways from KEGG website, extract the gene interaction relations, construct the KEGG pathway gene interaction network. The potential diagnostic markers of breast cancer were obtained by combining the differentially expressed genes with the key genes in the network. Finally, these markers were used to construct the diagnostic prediction model of breast cancer, and the predictive ability of the model and the diagnostic ability of the markers were verified by internal and external data. Results: 1060 differentially expressed genes were identified between breast cancer patients and normal controls. Enrichment analysis revealed 28 significantly enriched pathways (p < 0.05). They were downloaded from KEGG website, and the gene interaction relations were extracted to construct the gene interaction network of KEGG pathway, which contained 1277 nodes and 7345 edges. The key nodes with a degree greater than 30 were extracted from the network, containing 154 genes. These 154 key genes shared 23 genes with differentially expressed genes, which serve as potential diagnostic markers for breast cancer. The 23 genes were used as features to construct the SVM classification model, and the model had good predictive ability in both the training dataset and the validation dataset (AUC = 0.960 and 0.907, respectively). Conclusion: This study showed that the difference of gene expression level is important for the diagnosis of breast cancer, and identified 23 breast cancer diagnostic markers, which provides valuable information for clinical diagnosis and basic treatment experiments.
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spelling pubmed-87902932022-01-27 Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network Zhang, Shumei Jiang, Haoran Gao, Bo Yang, Wen Wang, Guohua Front Cell Dev Biol Cell and Developmental Biology Background: Breast cancer is the second largest cancer in the world, the incidence of breast cancer continues to rise worldwide, and women’s health is seriously threatened. Therefore, it is very important to explore the characteristic changes of breast cancer from the gene level, including the screening of differentially expressed genes and the identification of diagnostic markers. Methods: The gene expression profiles of breast cancer were obtained from the TCGA database. The edgeR R software package was used to screen the differentially expressed genes between breast cancer patients and normal samples. The function and pathway enrichment analysis of these genes revealed significant enrichment of functions and pathways. Next, download these pathways from KEGG website, extract the gene interaction relations, construct the KEGG pathway gene interaction network. The potential diagnostic markers of breast cancer were obtained by combining the differentially expressed genes with the key genes in the network. Finally, these markers were used to construct the diagnostic prediction model of breast cancer, and the predictive ability of the model and the diagnostic ability of the markers were verified by internal and external data. Results: 1060 differentially expressed genes were identified between breast cancer patients and normal controls. Enrichment analysis revealed 28 significantly enriched pathways (p < 0.05). They were downloaded from KEGG website, and the gene interaction relations were extracted to construct the gene interaction network of KEGG pathway, which contained 1277 nodes and 7345 edges. The key nodes with a degree greater than 30 were extracted from the network, containing 154 genes. These 154 key genes shared 23 genes with differentially expressed genes, which serve as potential diagnostic markers for breast cancer. The 23 genes were used as features to construct the SVM classification model, and the model had good predictive ability in both the training dataset and the validation dataset (AUC = 0.960 and 0.907, respectively). Conclusion: This study showed that the difference of gene expression level is important for the diagnosis of breast cancer, and identified 23 breast cancer diagnostic markers, which provides valuable information for clinical diagnosis and basic treatment experiments. Frontiers Media S.A. 2022-01-12 /pmc/articles/PMC8790293/ /pubmed/35096840 http://dx.doi.org/10.3389/fcell.2021.811585 Text en Copyright © 2022 Zhang, Jiang, Gao, Yang and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Zhang, Shumei
Jiang, Haoran
Gao, Bo
Yang, Wen
Wang, Guohua
Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network
title Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network
title_full Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network
title_fullStr Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network
title_full_unstemmed Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network
title_short Identification of Diagnostic Markers for Breast Cancer Based on Differential Gene Expression and Pathway Network
title_sort identification of diagnostic markers for breast cancer based on differential gene expression and pathway network
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790293/
https://www.ncbi.nlm.nih.gov/pubmed/35096840
http://dx.doi.org/10.3389/fcell.2021.811585
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