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Nicotinamide N-methyltransferase and liver diseases

Cellular metabolism-induced epigenetic regulation is essential for the maintenance of cellular homeostasis. Nicotinamide N-methyltransferase (NNMT) is emerging as a key point of intersection between cellular metabolism and epigenetic regulation and has a central role in various physiological and pat...

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Autores principales: Liang, Guangyu, Li, Ying, Lin, Yan, Yang, Xiao, Yang, Jiankun, Hu, Shaobo, Liu, Anding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363563/
https://www.ncbi.nlm.nih.gov/pubmed/37492717
http://dx.doi.org/10.1016/j.gendis.2022.03.019
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author Liang, Guangyu
Li, Ying
Lin, Yan
Yang, Xiao
Yang, Jiankun
Hu, Shaobo
Liu, Anding
author_facet Liang, Guangyu
Li, Ying
Lin, Yan
Yang, Xiao
Yang, Jiankun
Hu, Shaobo
Liu, Anding
author_sort Liang, Guangyu
collection PubMed
description Cellular metabolism-induced epigenetic regulation is essential for the maintenance of cellular homeostasis. Nicotinamide N-methyltransferase (NNMT) is emerging as a key point of intersection between cellular metabolism and epigenetic regulation and has a central role in various physiological and pathological processes. NNMT catalyzes the methylation of nicotinamide (NAM) using the universal methyl donor S-adenosyl methionine (SAM) to yield S-adeno-syl-L-homocysteine (SAH) and N1-methylnicotinamide (MNAM), directly linking methylation balance with nicotinamide adenosine dinucleotide (NAD(+)) contents. NNMT acts on either the SAM-methylation balance or both NAD(+) metabolism, depending on the tissue involved or pathological settings where metabolic demand is increased. Under physiological conditions, the liver act as an essential metabolic organ with abundant NNMT expression, while NNMT hepatic function is not mediated by its methyltransferase activity due to other major methyltransferases such as glycine N-methyltransferase (GNMT) in the liver. However, hepatic NNMT, as well as its metabolite is improperly regulated and linked to the worse pathological states in liver diseases, including alcoholic liver disease, non-alcoholic fatty liver disease (NAFLD), liver cirrhosis, and hepatocellular carcinoma (HCC), suggesting a potential role in the process of liver diseases. In this review, we summarize how NNMT regulates cell methylation balance and NAD metabolism, and extensively outline the current knowledge concerning the functions of NNMT in hepatic metabolism including glucose, lipid and energy, with a specific focus on the contribution of NNMT to the pathophysiology of liver-related diseases. NNMT is involved in the development and progression of liver diseases. Understanding the complex NNMT regulatory network and its effects on pathogenesis could provide new therapeutic strategies in the context of liver diseases.
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spelling pubmed-103635632023-07-25 Nicotinamide N-methyltransferase and liver diseases Liang, Guangyu Li, Ying Lin, Yan Yang, Xiao Yang, Jiankun Hu, Shaobo Liu, Anding Genes Dis Review Article Cellular metabolism-induced epigenetic regulation is essential for the maintenance of cellular homeostasis. Nicotinamide N-methyltransferase (NNMT) is emerging as a key point of intersection between cellular metabolism and epigenetic regulation and has a central role in various physiological and pathological processes. NNMT catalyzes the methylation of nicotinamide (NAM) using the universal methyl donor S-adenosyl methionine (SAM) to yield S-adeno-syl-L-homocysteine (SAH) and N1-methylnicotinamide (MNAM), directly linking methylation balance with nicotinamide adenosine dinucleotide (NAD(+)) contents. NNMT acts on either the SAM-methylation balance or both NAD(+) metabolism, depending on the tissue involved or pathological settings where metabolic demand is increased. Under physiological conditions, the liver act as an essential metabolic organ with abundant NNMT expression, while NNMT hepatic function is not mediated by its methyltransferase activity due to other major methyltransferases such as glycine N-methyltransferase (GNMT) in the liver. However, hepatic NNMT, as well as its metabolite is improperly regulated and linked to the worse pathological states in liver diseases, including alcoholic liver disease, non-alcoholic fatty liver disease (NAFLD), liver cirrhosis, and hepatocellular carcinoma (HCC), suggesting a potential role in the process of liver diseases. In this review, we summarize how NNMT regulates cell methylation balance and NAD metabolism, and extensively outline the current knowledge concerning the functions of NNMT in hepatic metabolism including glucose, lipid and energy, with a specific focus on the contribution of NNMT to the pathophysiology of liver-related diseases. NNMT is involved in the development and progression of liver diseases. Understanding the complex NNMT regulatory network and its effects on pathogenesis could provide new therapeutic strategies in the context of liver diseases. Chongqing Medical University 2022-04-20 /pmc/articles/PMC10363563/ /pubmed/37492717 http://dx.doi.org/10.1016/j.gendis.2022.03.019 Text en © 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Liang, Guangyu
Li, Ying
Lin, Yan
Yang, Xiao
Yang, Jiankun
Hu, Shaobo
Liu, Anding
Nicotinamide N-methyltransferase and liver diseases
title Nicotinamide N-methyltransferase and liver diseases
title_full Nicotinamide N-methyltransferase and liver diseases
title_fullStr Nicotinamide N-methyltransferase and liver diseases
title_full_unstemmed Nicotinamide N-methyltransferase and liver diseases
title_short Nicotinamide N-methyltransferase and liver diseases
title_sort nicotinamide n-methyltransferase and liver diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363563/
https://www.ncbi.nlm.nih.gov/pubmed/37492717
http://dx.doi.org/10.1016/j.gendis.2022.03.019
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