m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment

Background. We analyzed the n6-methyladenosine (m6A) modification patterns of immune cells infiltrating the tumor microenvironment of breast cancer (BC) to provide a new perspective for the early diagnosis and treatment of BC. Methods. Based on 23 m6A regulatory factors, we identified m6A-related ge...

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Autores principales: Fei Liu, Xiaopeng Yu, Guijin He
Formato: article
Lenguaje:EN
Publicado: Hindawi Limited 2021
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Acceso en línea:https://doaj.org/article/5ba0801ab1584a1aba77e43ac0c82644
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spelling oai:doaj.org-article:5ba0801ab1584a1aba77e43ac0c826442021-11-08T02:36:38Zm6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment1687-846910.1155/2021/9987376https://doaj.org/article/5ba0801ab1584a1aba77e43ac0c826442021-01-01T00:00:00Zhttp://dx.doi.org/10.1155/2021/9987376https://doaj.org/toc/1687-8469Background. We analyzed the n6-methyladenosine (m6A) modification patterns of immune cells infiltrating the tumor microenvironment of breast cancer (BC) to provide a new perspective for the early diagnosis and treatment of BC. Methods. Based on 23 m6A regulatory factors, we identified m6A-related gene characteristics and m6A modification patterns in BC through unsupervised cluster analysis. To examine the differences in biological processes among various m6A modification modes, we performed genomic variation analysis. We then quantified the relative infiltration levels of different immune cell subpopulations in the tumor microenvironment of BC using the CIBERSORT algorithm and single-sample gene set enrichment analysis. Univariate Cox analysis was used to screen for m6A characteristic genes related to prognosis. Finally, we evaluated the m6A modification pattern of patients with a single BC by constructing the m6Ascore based on principal component analysis. Results. We identified three different m6A modification patterns in 2128 BC samples. A higher abundance of the immune infiltration of the m6Acluster C was indicated by the results of CIBERSORT and the single-sample gene set enrichment analysis. Based on the m6A characteristic genes obtained through screening, the m6Ascore was determined. The BC patients were segregated into m6Ascore groups of low and high categories, which revealed significant survival benefits among patients with low m6Ascores. Additionally, the high-m6Ascore group had a higher mutation frequency and was associated with low PD-L1 expression, and the m6Ascore and tumor mutation burden showed a positive correlation. In addition, treatment effects were better in patients in the high-m6Ascore group. Conclusions. In case of a single patient with BC, the immune cell infiltration characteristics of the tumor microenvironment and the m6A methylation modification pattern could be evaluated using the m6Ascore. Our results provide a foundation for improving personalized immunotherapy of BC.Fei LiuXiaopeng YuGuijin HeHindawi LimitedarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENJournal of Oncology, Vol 2021 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Fei Liu
Xiaopeng Yu
Guijin He
m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment
description Background. We analyzed the n6-methyladenosine (m6A) modification patterns of immune cells infiltrating the tumor microenvironment of breast cancer (BC) to provide a new perspective for the early diagnosis and treatment of BC. Methods. Based on 23 m6A regulatory factors, we identified m6A-related gene characteristics and m6A modification patterns in BC through unsupervised cluster analysis. To examine the differences in biological processes among various m6A modification modes, we performed genomic variation analysis. We then quantified the relative infiltration levels of different immune cell subpopulations in the tumor microenvironment of BC using the CIBERSORT algorithm and single-sample gene set enrichment analysis. Univariate Cox analysis was used to screen for m6A characteristic genes related to prognosis. Finally, we evaluated the m6A modification pattern of patients with a single BC by constructing the m6Ascore based on principal component analysis. Results. We identified three different m6A modification patterns in 2128 BC samples. A higher abundance of the immune infiltration of the m6Acluster C was indicated by the results of CIBERSORT and the single-sample gene set enrichment analysis. Based on the m6A characteristic genes obtained through screening, the m6Ascore was determined. The BC patients were segregated into m6Ascore groups of low and high categories, which revealed significant survival benefits among patients with low m6Ascores. Additionally, the high-m6Ascore group had a higher mutation frequency and was associated with low PD-L1 expression, and the m6Ascore and tumor mutation burden showed a positive correlation. In addition, treatment effects were better in patients in the high-m6Ascore group. Conclusions. In case of a single patient with BC, the immune cell infiltration characteristics of the tumor microenvironment and the m6A methylation modification pattern could be evaluated using the m6Ascore. Our results provide a foundation for improving personalized immunotherapy of BC.
format article
author Fei Liu
Xiaopeng Yu
Guijin He
author_facet Fei Liu
Xiaopeng Yu
Guijin He
author_sort Fei Liu
title m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment
title_short m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment
title_full m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment
title_fullStr m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment
title_full_unstemmed m6A-Mediated Tumor Invasion and Methylation Modification in Breast Cancer Microenvironment
title_sort m6a-mediated tumor invasion and methylation modification in breast cancer microenvironment
publisher Hindawi Limited
publishDate 2021
url https://doaj.org/article/5ba0801ab1584a1aba77e43ac0c82644
work_keys_str_mv AT feiliu m6amediatedtumorinvasionandmethylationmodificationinbreastcancermicroenvironment
AT xiaopengyu m6amediatedtumorinvasionandmethylationmodificationinbreastcancermicroenvironment
AT guijinhe m6amediatedtumorinvasionandmethylationmodificationinbreastcancermicroenvironment
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