Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis

Breast cancer (BC) is the leading cause of cancer death among women worldwide. The molecular mechanisms of its pathogenesis are still to be investigated. In our study, differentially expressed genes (DEGs) were screened between BC and normal tissues. Based on the DEGs, a weighted gene co-expression...

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Main Authors: Gengsheng Shi, Zhenru Shen, Yi Liu, Wenqin Yin
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2020.597888/full
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spelling doaj-c6bebaa1809345eebab4cb9b52986a382020-12-17T07:13:21ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-12-011110.3389/fgene.2020.597888597888Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network AnalysisGengsheng Shi0Zhenru Shen1Yi Liu2Wenqin Yin3Department of Clinical and Public Health, School of Health and Rehabilitation, Jiangsu College of Nursing, Jiangsu, ChinaDepartment of Cardiothoracic Surgery, The Second People’s Hospital of Huai’an, Huai’an, ChinaDepartment of Clinical and Public Health, School of Health and Rehabilitation, Jiangsu College of Nursing, Jiangsu, ChinaDepartment of Clinical and Public Health, School of Health and Rehabilitation, Jiangsu College of Nursing, Jiangsu, ChinaBreast cancer (BC) is the leading cause of cancer death among women worldwide. The molecular mechanisms of its pathogenesis are still to be investigated. In our study, differentially expressed genes (DEGs) were screened between BC and normal tissues. Based on the DEGs, a weighted gene co-expression network analysis (WGCNA) was performed in 683 BC samples, and eight co-expressed gene modules were identified. In addition, by relating the eight co-expressed modules to clinical information, we found the blue module and pathological stage had a significant correlation (r = 0.24, p = 1e–10). Validated by multiple independent datasets, using one-way ANOVA, survival analysis and expression level revalidation, we finally screened 12 hub genes that can predict BC progression and prognosis. Functional annotation analysis indicated that the hub genes were enriched in cell division and cell cycle regulation. Importantly, higher expression of the 12 hub genes indicated poor overall survival, recurrence-free survival, and disease-free survival in BC patients. In addition, the expression of the 12 hub genes showed a significantly positive correlation with the expression of cell proliferation marker Ki-67 in BC. In summary, our study has identified 12 hub genes associated with the progression and prognosis of BC; these hub genes might lead to poor outcomes by regulating the cell division and cell cycle. These hub genes may serve as a biomarker and help to distinguish different pathological stages for BC patients.https://www.frontiersin.org/articles/10.3389/fgene.2020.597888/fullbreast cancerWGCNAprogressioncell cycleprognosis
collection DOAJ
language English
format Article
sources DOAJ
author Gengsheng Shi
Zhenru Shen
Yi Liu
Wenqin Yin
spellingShingle Gengsheng Shi
Zhenru Shen
Yi Liu
Wenqin Yin
Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis
Frontiers in Genetics
breast cancer
WGCNA
progression
cell cycle
prognosis
author_facet Gengsheng Shi
Zhenru Shen
Yi Liu
Wenqin Yin
author_sort Gengsheng Shi
title Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis
title_short Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis
title_full Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis
title_fullStr Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis
title_full_unstemmed Identifying Biomarkers to Predict the Progression and Prognosis of Breast Cancer by Weighted Gene Co-expression Network Analysis
title_sort identifying biomarkers to predict the progression and prognosis of breast cancer by weighted gene co-expression network analysis
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2020-12-01
description Breast cancer (BC) is the leading cause of cancer death among women worldwide. The molecular mechanisms of its pathogenesis are still to be investigated. In our study, differentially expressed genes (DEGs) were screened between BC and normal tissues. Based on the DEGs, a weighted gene co-expression network analysis (WGCNA) was performed in 683 BC samples, and eight co-expressed gene modules were identified. In addition, by relating the eight co-expressed modules to clinical information, we found the blue module and pathological stage had a significant correlation (r = 0.24, p = 1e–10). Validated by multiple independent datasets, using one-way ANOVA, survival analysis and expression level revalidation, we finally screened 12 hub genes that can predict BC progression and prognosis. Functional annotation analysis indicated that the hub genes were enriched in cell division and cell cycle regulation. Importantly, higher expression of the 12 hub genes indicated poor overall survival, recurrence-free survival, and disease-free survival in BC patients. In addition, the expression of the 12 hub genes showed a significantly positive correlation with the expression of cell proliferation marker Ki-67 in BC. In summary, our study has identified 12 hub genes associated with the progression and prognosis of BC; these hub genes might lead to poor outcomes by regulating the cell division and cell cycle. These hub genes may serve as a biomarker and help to distinguish different pathological stages for BC patients.
topic breast cancer
WGCNA
progression
cell cycle
prognosis
url https://www.frontiersin.org/articles/10.3389/fgene.2020.597888/full
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