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m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival

Numerous studies have demonstrated the important roles of epigenetic modifications in tumorigenesis, progression and prognosis. However, in hepatocellular carcinoma, the potential link between N(7)-methylguanosine (m(7)G) modification and molecular heterogeneity and tumor microenvironment (TME) rema...

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Autores principales: Wang, Lu, Hu, Xing, Liu, Xiaoni, Feng, Yingmei, Zhang, Yuan, Han, Jing, Liu, Xuqing, Meng, Fankun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650241/
https://www.ncbi.nlm.nih.gov/pubmed/36389726
http://dx.doi.org/10.3389/fimmu.2022.1022720
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author Wang, Lu
Hu, Xing
Liu, Xiaoni
Feng, Yingmei
Zhang, Yuan
Han, Jing
Liu, Xuqing
Meng, Fankun
author_facet Wang, Lu
Hu, Xing
Liu, Xiaoni
Feng, Yingmei
Zhang, Yuan
Han, Jing
Liu, Xuqing
Meng, Fankun
author_sort Wang, Lu
collection PubMed
description Numerous studies have demonstrated the important roles of epigenetic modifications in tumorigenesis, progression and prognosis. However, in hepatocellular carcinoma, the potential link between N(7)-methylguanosine (m(7)G) modification and molecular heterogeneity and tumor microenvironment (TME) remains unclear. METHOD: We performed a comprehensive evaluation of m(7)G modification patterns in 816 hepatocellular carcinoma samples based on 24 m(7)G regulatory factors, identified different m(7)G modification patterns, and made a systematic correlation of these modification patterns with the infiltration characteristics of immunocytes. Then, we built and validated a scoring tool called m(7)G score. RESULTS: In this study, we revealed the presence of three distinct m(7)G modification patterns in liver cancer, with remarkable differences in the immunocyte infiltration characteristics of these three subtypes. The m(7)G scoring system of this study could assess m(7)G modification patterns in individual hepatocellular carcinoma patients, could predict TME infiltration characteristics, genetic variants and patient prognosis. We also found that the m(7)G scoring system may be useful in guiding patients’ clinical use of medications. CONCLUSIONS: This study revealed that m(7)G methylation modifications exerted a significant role in formation of TME in hepatocellular carcinoma. Assessing the m(7)G modification patterns of single patients would help enhance our perception of TME infiltration characteristics and give significant insights into immunotherapy efficacy.
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spelling pubmed-96502412022-11-15 m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival Wang, Lu Hu, Xing Liu, Xiaoni Feng, Yingmei Zhang, Yuan Han, Jing Liu, Xuqing Meng, Fankun Front Immunol Immunology Numerous studies have demonstrated the important roles of epigenetic modifications in tumorigenesis, progression and prognosis. However, in hepatocellular carcinoma, the potential link between N(7)-methylguanosine (m(7)G) modification and molecular heterogeneity and tumor microenvironment (TME) remains unclear. METHOD: We performed a comprehensive evaluation of m(7)G modification patterns in 816 hepatocellular carcinoma samples based on 24 m(7)G regulatory factors, identified different m(7)G modification patterns, and made a systematic correlation of these modification patterns with the infiltration characteristics of immunocytes. Then, we built and validated a scoring tool called m(7)G score. RESULTS: In this study, we revealed the presence of three distinct m(7)G modification patterns in liver cancer, with remarkable differences in the immunocyte infiltration characteristics of these three subtypes. The m(7)G scoring system of this study could assess m(7)G modification patterns in individual hepatocellular carcinoma patients, could predict TME infiltration characteristics, genetic variants and patient prognosis. We also found that the m(7)G scoring system may be useful in guiding patients’ clinical use of medications. CONCLUSIONS: This study revealed that m(7)G methylation modifications exerted a significant role in formation of TME in hepatocellular carcinoma. Assessing the m(7)G modification patterns of single patients would help enhance our perception of TME infiltration characteristics and give significant insights into immunotherapy efficacy. Frontiers Media S.A. 2022-10-28 /pmc/articles/PMC9650241/ /pubmed/36389726 http://dx.doi.org/10.3389/fimmu.2022.1022720 Text en Copyright © 2022 Wang, Hu, Liu, Feng, Zhang, Han, Liu and Meng 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 Immunology
Wang, Lu
Hu, Xing
Liu, Xiaoni
Feng, Yingmei
Zhang, Yuan
Han, Jing
Liu, Xuqing
Meng, Fankun
m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
title m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
title_full m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
title_fullStr m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
title_full_unstemmed m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
title_short m(7)G regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
title_sort m(7)g regulator-mediated methylation modification patterns define immune cell infiltration and patient survival
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650241/
https://www.ncbi.nlm.nih.gov/pubmed/36389726
http://dx.doi.org/10.3389/fimmu.2022.1022720
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