DNA methylation profiles capturing breast cancer heterogeneity

Abstract Background As one of the most described epigenetic marks in human cancers, DNA methylation plays essential roles in gene expression regulation and has been implicated in the prognosis and therapeutics of many cancers. We are motivated in this study to explore DNA methylation profiles captur...

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Main Authors: Xiao Chen, Jianying Zhang, Xiaofeng Dai
Format: Article
Language:English
Published: BMC 2019-11-01
Series:BMC Genomics
Online Access:http://link.springer.com/article/10.1186/s12864-019-6142-y
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author Xiao Chen
Jianying Zhang
Xiaofeng Dai
author_facet Xiao Chen
Jianying Zhang
Xiaofeng Dai
author_sort Xiao Chen
collection DOAJ
description Abstract Background As one of the most described epigenetic marks in human cancers, DNA methylation plays essential roles in gene expression regulation and has been implicated in the prognosis and therapeutics of many cancers. We are motivated in this study to explore DNA methylation profiles capturing breast cancer heterogeneity to improve breast cancer prognosis at the epigenetic level. Results Through comparisons on differentially methylated CpG sites among breast cancer subtypes followed by a sequential validation and functional studies using computational approaches, we propose 313 CpG, corresponding to 191 genes, whose methylation pattern identifies the triple negative breast cancer subtype, and report cell migration as represented by extracellular matrix organization and cell proliferation as mediated via MAPK and Wnt signalings are the primary factors driving breast cancer subtyping. Conclusions Our study offers novel CpGs and gene methylation patterns with translational potential on triple negative breast cancer prognosis, as well as fresh insights from the epigenetic level on breast cancer heterogeneity.
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spelling doaj.art-235096b055594028ae15c9f3cc2bb0532022-12-21T22:46:47ZengBMCBMC Genomics1471-21642019-11-0120111210.1186/s12864-019-6142-yDNA methylation profiles capturing breast cancer heterogeneityXiao Chen0Jianying Zhang1Xiaofeng Dai2School of Biotechnology, Jiangnan UniversityHenan Academy of Medical and Pharmaceutical Sciences, Zhengzhou UniversityWuxi School of Medicine, Jiangnan UniversityAbstract Background As one of the most described epigenetic marks in human cancers, DNA methylation plays essential roles in gene expression regulation and has been implicated in the prognosis and therapeutics of many cancers. We are motivated in this study to explore DNA methylation profiles capturing breast cancer heterogeneity to improve breast cancer prognosis at the epigenetic level. Results Through comparisons on differentially methylated CpG sites among breast cancer subtypes followed by a sequential validation and functional studies using computational approaches, we propose 313 CpG, corresponding to 191 genes, whose methylation pattern identifies the triple negative breast cancer subtype, and report cell migration as represented by extracellular matrix organization and cell proliferation as mediated via MAPK and Wnt signalings are the primary factors driving breast cancer subtyping. Conclusions Our study offers novel CpGs and gene methylation patterns with translational potential on triple negative breast cancer prognosis, as well as fresh insights from the epigenetic level on breast cancer heterogeneity.http://link.springer.com/article/10.1186/s12864-019-6142-y
spellingShingle Xiao Chen
Jianying Zhang
Xiaofeng Dai
DNA methylation profiles capturing breast cancer heterogeneity
BMC Genomics
title DNA methylation profiles capturing breast cancer heterogeneity
title_full DNA methylation profiles capturing breast cancer heterogeneity
title_fullStr DNA methylation profiles capturing breast cancer heterogeneity
title_full_unstemmed DNA methylation profiles capturing breast cancer heterogeneity
title_short DNA methylation profiles capturing breast cancer heterogeneity
title_sort dna methylation profiles capturing breast cancer heterogeneity
url http://link.springer.com/article/10.1186/s12864-019-6142-y
work_keys_str_mv AT xiaochen dnamethylationprofilescapturingbreastcancerheterogeneity
AT jianyingzhang dnamethylationprofilescapturingbreastcancerheterogeneity
AT xiaofengdai dnamethylationprofilescapturingbreastcancerheterogeneity