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A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer

The immune system can monitor tumor development, and DNA methylation is involved in the body’s immune response to tumors. In this work, we investigate whether DNA methylation alterations in peripheral blood mononuclear cells (PBMCs) could be used as markers for early detection of breast cancer (BC)...

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Autores principales: Wang, Tiantian, Li, Peilong, Qi, Qiuchen, Zhang, Shujun, Xie, Yan, Wang, Jing, Liu, Shibiao, Ma, Suhong, Li, Shijun, Gong, Tingting, Xu, Huiting, Xiong, Mengqiu, Li, Guanghua, You, Chongge, Luo, Zhaofan, Li, Juan, Du, Lutao, Wang, Chuanxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406825/
https://www.ncbi.nlm.nih.gov/pubmed/37550304
http://dx.doi.org/10.1038/s41467-023-40389-5
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author Wang, Tiantian
Li, Peilong
Qi, Qiuchen
Zhang, Shujun
Xie, Yan
Wang, Jing
Liu, Shibiao
Ma, Suhong
Li, Shijun
Gong, Tingting
Xu, Huiting
Xiong, Mengqiu
Li, Guanghua
You, Chongge
Luo, Zhaofan
Li, Juan
Du, Lutao
Wang, Chuanxin
author_facet Wang, Tiantian
Li, Peilong
Qi, Qiuchen
Zhang, Shujun
Xie, Yan
Wang, Jing
Liu, Shibiao
Ma, Suhong
Li, Shijun
Gong, Tingting
Xu, Huiting
Xiong, Mengqiu
Li, Guanghua
You, Chongge
Luo, Zhaofan
Li, Juan
Du, Lutao
Wang, Chuanxin
author_sort Wang, Tiantian
collection PubMed
description The immune system can monitor tumor development, and DNA methylation is involved in the body’s immune response to tumors. In this work, we investigate whether DNA methylation alterations in peripheral blood mononuclear cells (PBMCs) could be used as markers for early detection of breast cancer (BC) from the perspective of tumor immune alterations. We identify four BC-specific methylation markers by combining Infinium 850 K BeadChips, pyrosequencing and targeted bisulfite sequencing. Based on the four methylation markers in PBMCs of BC, we develop an efficient and convenient multiplex methylation-specific quantitative PCR assay for the detection of BC and validate its diagnostic performance in a multicenter cohort. This assay was able to distinguish early-stage BC patients from normal controls, with an AUC of 0.940, sensitivity of 93.2%, and specificity of 90.4%. More importantly, this assay outperformed existing clinical diagnostic methods, especially in the detection of early-stage and minimal tumors.
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spelling pubmed-104068252023-08-09 A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer Wang, Tiantian Li, Peilong Qi, Qiuchen Zhang, Shujun Xie, Yan Wang, Jing Liu, Shibiao Ma, Suhong Li, Shijun Gong, Tingting Xu, Huiting Xiong, Mengqiu Li, Guanghua You, Chongge Luo, Zhaofan Li, Juan Du, Lutao Wang, Chuanxin Nat Commun Article The immune system can monitor tumor development, and DNA methylation is involved in the body’s immune response to tumors. In this work, we investigate whether DNA methylation alterations in peripheral blood mononuclear cells (PBMCs) could be used as markers for early detection of breast cancer (BC) from the perspective of tumor immune alterations. We identify four BC-specific methylation markers by combining Infinium 850 K BeadChips, pyrosequencing and targeted bisulfite sequencing. Based on the four methylation markers in PBMCs of BC, we develop an efficient and convenient multiplex methylation-specific quantitative PCR assay for the detection of BC and validate its diagnostic performance in a multicenter cohort. This assay was able to distinguish early-stage BC patients from normal controls, with an AUC of 0.940, sensitivity of 93.2%, and specificity of 90.4%. More importantly, this assay outperformed existing clinical diagnostic methods, especially in the detection of early-stage and minimal tumors. Nature Publishing Group UK 2023-08-07 /pmc/articles/PMC10406825/ /pubmed/37550304 http://dx.doi.org/10.1038/s41467-023-40389-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Tiantian
Li, Peilong
Qi, Qiuchen
Zhang, Shujun
Xie, Yan
Wang, Jing
Liu, Shibiao
Ma, Suhong
Li, Shijun
Gong, Tingting
Xu, Huiting
Xiong, Mengqiu
Li, Guanghua
You, Chongge
Luo, Zhaofan
Li, Juan
Du, Lutao
Wang, Chuanxin
A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer
title A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer
title_full A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer
title_fullStr A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer
title_full_unstemmed A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer
title_short A multiplex blood-based assay targeting DNA methylation in PBMCs enables early detection of breast cancer
title_sort multiplex blood-based assay targeting dna methylation in pbmcs enables early detection of breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406825/
https://www.ncbi.nlm.nih.gov/pubmed/37550304
http://dx.doi.org/10.1038/s41467-023-40389-5
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