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Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers

Altered metabolic patterns in tumor cells not only meet their own growth requirements but also shape an immunosuppressive microenvironment through multiple mechanisms. Noncoding RNAs constitute approximately 60% of the transcriptional output of human cells and have been shown to regulate numerous ce...

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Autores principales: Zhang, Yiyin, Mao, Qijiang, Xia, Qiming, Cheng, Jiaxi, Huang, Zhengze, Li, Yirun, Chen, Peng, Yang, Jing, Fan, Xiaoxiao, Liang, Yuelong, Lin, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518176/
https://www.ncbi.nlm.nih.gov/pubmed/34654454
http://dx.doi.org/10.1186/s13045-021-01179-y
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author Zhang, Yiyin
Mao, Qijiang
Xia, Qiming
Cheng, Jiaxi
Huang, Zhengze
Li, Yirun
Chen, Peng
Yang, Jing
Fan, Xiaoxiao
Liang, Yuelong
Lin, Hui
author_facet Zhang, Yiyin
Mao, Qijiang
Xia, Qiming
Cheng, Jiaxi
Huang, Zhengze
Li, Yirun
Chen, Peng
Yang, Jing
Fan, Xiaoxiao
Liang, Yuelong
Lin, Hui
author_sort Zhang, Yiyin
collection PubMed
description Altered metabolic patterns in tumor cells not only meet their own growth requirements but also shape an immunosuppressive microenvironment through multiple mechanisms. Noncoding RNAs constitute approximately 60% of the transcriptional output of human cells and have been shown to regulate numerous cellular processes under developmental and pathological conditions. Given their extensive action mechanisms based on motif recognition patterns, noncoding RNAs may serve as hinges bridging metabolic activity and immune responses. Indeed, recent studies have shown that microRNAs, long noncoding RNAs and circRNAs are widely involved in tumor metabolic rewiring, immune cell infiltration and function. Hence, we summarized existing knowledge of the role of noncoding RNAs in the remodeling of tumor metabolism and the immune microenvironment, and notably, we established the TIMELnc manual, which is a free and public manual for researchers to identify pivotal lncRNAs that are simultaneously correlated with tumor metabolism and immune cell infiltration based on a bioinformatic approach. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-021-01179-y.
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spelling pubmed-85181762021-10-20 Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers Zhang, Yiyin Mao, Qijiang Xia, Qiming Cheng, Jiaxi Huang, Zhengze Li, Yirun Chen, Peng Yang, Jing Fan, Xiaoxiao Liang, Yuelong Lin, Hui J Hematol Oncol Review Altered metabolic patterns in tumor cells not only meet their own growth requirements but also shape an immunosuppressive microenvironment through multiple mechanisms. Noncoding RNAs constitute approximately 60% of the transcriptional output of human cells and have been shown to regulate numerous cellular processes under developmental and pathological conditions. Given their extensive action mechanisms based on motif recognition patterns, noncoding RNAs may serve as hinges bridging metabolic activity and immune responses. Indeed, recent studies have shown that microRNAs, long noncoding RNAs and circRNAs are widely involved in tumor metabolic rewiring, immune cell infiltration and function. Hence, we summarized existing knowledge of the role of noncoding RNAs in the remodeling of tumor metabolism and the immune microenvironment, and notably, we established the TIMELnc manual, which is a free and public manual for researchers to identify pivotal lncRNAs that are simultaneously correlated with tumor metabolism and immune cell infiltration based on a bioinformatic approach. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-021-01179-y. BioMed Central 2021-10-15 /pmc/articles/PMC8518176/ /pubmed/34654454 http://dx.doi.org/10.1186/s13045-021-01179-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Zhang, Yiyin
Mao, Qijiang
Xia, Qiming
Cheng, Jiaxi
Huang, Zhengze
Li, Yirun
Chen, Peng
Yang, Jing
Fan, Xiaoxiao
Liang, Yuelong
Lin, Hui
Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers
title Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers
title_full Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers
title_fullStr Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers
title_full_unstemmed Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers
title_short Noncoding RNAs link metabolic reprogramming to immune microenvironment in cancers
title_sort noncoding rnas link metabolic reprogramming to immune microenvironment in cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518176/
https://www.ncbi.nlm.nih.gov/pubmed/34654454
http://dx.doi.org/10.1186/s13045-021-01179-y
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