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Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs
Pediatric central nervous system (CNS) tumors are the second most common cancer diagnosis among children. Long noncoding RNAs (lncRNAs) emerge as critical regulators of gene expression, and they play fundamental roles in immune regulation. However, knowledge on epigenetic changes in lncRNAs in diver...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114481/ https://www.ncbi.nlm.nih.gov/pubmed/35603200 http://dx.doi.org/10.3389/fimmu.2022.853904 |
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author | Li, Yongsheng Xu, Sicong Xu, Dahua Pan, Tao Guo, Jing Gu, Shuo Lin, Qiuyu Li, Xia Li, Kongning Xiang, Wei |
author_facet | Li, Yongsheng Xu, Sicong Xu, Dahua Pan, Tao Guo, Jing Gu, Shuo Lin, Qiuyu Li, Xia Li, Kongning Xiang, Wei |
author_sort | Li, Yongsheng |
collection | PubMed |
description | Pediatric central nervous system (CNS) tumors are the second most common cancer diagnosis among children. Long noncoding RNAs (lncRNAs) emerge as critical regulators of gene expression, and they play fundamental roles in immune regulation. However, knowledge on epigenetic changes in lncRNAs in diverse types of pediatric CNS tumors is lacking. Here, we integrated the DNA methylation profiles of 2,257 pediatric CNS tumors across 61 subtypes with lncRNA annotations and presented the epigenetically regulated landscape of lncRNAs. We revealed the prevalent lncRNA methylation heterogeneity across pediatric pan-CNS tumors. Based on lncRNA methylation profiles, we refined 14 lncRNA methylation clusters with distinct immune microenvironment patterns. Moreover, we found that lncRNA methylations were significantly correlated with immune cell infiltrations in diverse tumor subtypes. Immune-related lncRNAs were further identified by investigating their correlation with immune cell infiltrations and potentially regulated target genes. LncRNA with methylation perturbations potentially regulate the genes in immune-related pathways. We finally identified several candidate immune-related lncRNA biomarkers (i.e., SSTR5-AS1, CNTN4-AS1, and OSTM1-AS1) in pediatric cancer for further functional validation. In summary, our study represents a comprehensive repertoire of epigenetically regulated immune-related lncRNAs in pediatric pan-CNS tumors, and will facilitate the development of immunotherapeutic targets. |
format | Online Article Text |
id | pubmed-9114481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91144812022-05-19 Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs Li, Yongsheng Xu, Sicong Xu, Dahua Pan, Tao Guo, Jing Gu, Shuo Lin, Qiuyu Li, Xia Li, Kongning Xiang, Wei Front Immunol Immunology Pediatric central nervous system (CNS) tumors are the second most common cancer diagnosis among children. Long noncoding RNAs (lncRNAs) emerge as critical regulators of gene expression, and they play fundamental roles in immune regulation. However, knowledge on epigenetic changes in lncRNAs in diverse types of pediatric CNS tumors is lacking. Here, we integrated the DNA methylation profiles of 2,257 pediatric CNS tumors across 61 subtypes with lncRNA annotations and presented the epigenetically regulated landscape of lncRNAs. We revealed the prevalent lncRNA methylation heterogeneity across pediatric pan-CNS tumors. Based on lncRNA methylation profiles, we refined 14 lncRNA methylation clusters with distinct immune microenvironment patterns. Moreover, we found that lncRNA methylations were significantly correlated with immune cell infiltrations in diverse tumor subtypes. Immune-related lncRNAs were further identified by investigating their correlation with immune cell infiltrations and potentially regulated target genes. LncRNA with methylation perturbations potentially regulate the genes in immune-related pathways. We finally identified several candidate immune-related lncRNA biomarkers (i.e., SSTR5-AS1, CNTN4-AS1, and OSTM1-AS1) in pediatric cancer for further functional validation. In summary, our study represents a comprehensive repertoire of epigenetically regulated immune-related lncRNAs in pediatric pan-CNS tumors, and will facilitate the development of immunotherapeutic targets. Frontiers Media S.A. 2022-05-04 /pmc/articles/PMC9114481/ /pubmed/35603200 http://dx.doi.org/10.3389/fimmu.2022.853904 Text en Copyright © 2022 Li, Xu, Xu, Pan, Guo, Gu, Lin, Li, Li and Xiang 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 Li, Yongsheng Xu, Sicong Xu, Dahua Pan, Tao Guo, Jing Gu, Shuo Lin, Qiuyu Li, Xia Li, Kongning Xiang, Wei Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs |
title | Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs |
title_full | Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs |
title_fullStr | Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs |
title_full_unstemmed | Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs |
title_short | Pediatric Pan-Central Nervous System Tumor Methylome Analyses Reveal Immune-Related LncRNAs |
title_sort | pediatric pan-central nervous system tumor methylome analyses reveal immune-related lncrnas |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114481/ https://www.ncbi.nlm.nih.gov/pubmed/35603200 http://dx.doi.org/10.3389/fimmu.2022.853904 |
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