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m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma

BACKGROUND: The dysregulation of RNA methylation has been demonstrated to contribute to tumorigenicity and progression in recent years. However, the alteration of N1-methyladenosine (m1A) methylation and its role in hepatocellular carcinoma (HCC) remain unclear. METHODS: We systematically investigat...

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Autores principales: Tong, Chengcheng, Wang, Wei, He, Chiyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896097/
https://www.ncbi.nlm.nih.gov/pubmed/35240991
http://dx.doi.org/10.1186/s12876-022-02160-w
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author Tong, Chengcheng
Wang, Wei
He, Chiyi
author_facet Tong, Chengcheng
Wang, Wei
He, Chiyi
author_sort Tong, Chengcheng
collection PubMed
description BACKGROUND: The dysregulation of RNA methylation has been demonstrated to contribute to tumorigenicity and progression in recent years. However, the alteration of N1-methyladenosine (m1A) methylation and its role in hepatocellular carcinoma (HCC) remain unclear. METHODS: We systematically investigated the modification patterns of 10 m1A regulators in HCC samples and evaluated the metabolic characteristics of each pattern. A scoring system named the m1Ascore was developed using principal component analysis. The clinical value of the m1Ascore in risk stratification and drug screening was further explored. RESULTS: Three m1A modification patterns with distinct metabolic characteristics were identified, corresponding to the metabolism-high, metabolism-intermediate and metabolism-excluded phenotypes. Patients were divided into high- or low-m1Ascore groups, and a significant survival difference was observed. External validation confirmed the prognostic value of the m1Ascore. A nomogram incorporating the m1Ascore and other clinicopathological factors was constructed and had good performance for predicting survival. Two agents, mitoxantrone and doxorubicin, were determined to be potential therapeutic drugs for the high-risk group. CONCLUSION: This study provided novel insights into m1A modification and metabolic heterogeneity in cancer, promoted risk stratification in the clinic from the perspective of m1A modification, and further guided individual treatment strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02160-w.
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spelling pubmed-88960972022-03-10 m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma Tong, Chengcheng Wang, Wei He, Chiyi BMC Gastroenterol Research Article BACKGROUND: The dysregulation of RNA methylation has been demonstrated to contribute to tumorigenicity and progression in recent years. However, the alteration of N1-methyladenosine (m1A) methylation and its role in hepatocellular carcinoma (HCC) remain unclear. METHODS: We systematically investigated the modification patterns of 10 m1A regulators in HCC samples and evaluated the metabolic characteristics of each pattern. A scoring system named the m1Ascore was developed using principal component analysis. The clinical value of the m1Ascore in risk stratification and drug screening was further explored. RESULTS: Three m1A modification patterns with distinct metabolic characteristics were identified, corresponding to the metabolism-high, metabolism-intermediate and metabolism-excluded phenotypes. Patients were divided into high- or low-m1Ascore groups, and a significant survival difference was observed. External validation confirmed the prognostic value of the m1Ascore. A nomogram incorporating the m1Ascore and other clinicopathological factors was constructed and had good performance for predicting survival. Two agents, mitoxantrone and doxorubicin, were determined to be potential therapeutic drugs for the high-risk group. CONCLUSION: This study provided novel insights into m1A modification and metabolic heterogeneity in cancer, promoted risk stratification in the clinic from the perspective of m1A modification, and further guided individual treatment strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02160-w. BioMed Central 2022-03-03 /pmc/articles/PMC8896097/ /pubmed/35240991 http://dx.doi.org/10.1186/s12876-022-02160-w Text en © The Author(s) 2022 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 Research Article
Tong, Chengcheng
Wang, Wei
He, Chiyi
m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
title m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
title_full m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
title_fullStr m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
title_full_unstemmed m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
title_short m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
title_sort m1a methylation modification patterns and metabolic characteristics in hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896097/
https://www.ncbi.nlm.nih.gov/pubmed/35240991
http://dx.doi.org/10.1186/s12876-022-02160-w
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