The emerging role of N6-methyladenine RNA methylation in metal ion metabolism and metal-induced carcinogenesis

N6-methyladenine (m6A) is the most common and abundant internal modification in eukaryotic mRNAs, which can regulate gene expression and perform important biological tasks. Metal ions participate in nucleotide biosynthesis and repair, signal transduction, energy generation, immune defense, and other...

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Veröffentlicht in:Environmental pollution (1987) 2023-08, Vol.331, p.121897-121897, Article 121897
Hauptverfasser: Liang, Yaxu, Wang, Huan, Wu, Bencheng, Peng, Ning, Yu, Dongming, Wu, Xin, Zhong, Xiang
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container_title Environmental pollution (1987)
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creator Liang, Yaxu
Wang, Huan
Wu, Bencheng
Peng, Ning
Yu, Dongming
Wu, Xin
Zhong, Xiang
description N6-methyladenine (m6A) is the most common and abundant internal modification in eukaryotic mRNAs, which can regulate gene expression and perform important biological tasks. Metal ions participate in nucleotide biosynthesis and repair, signal transduction, energy generation, immune defense, and other important metabolic processes. However, long-term environmental and occupational exposure to metals through food, air, soil, water, and industry can result in toxicity, serious health problems, and cancer. Recent evidence indicates dynamic and reversible m6A modification modulates various metal ion metabolism, such as iron absorption, calcium uptake and transport. In turn, environmental heavy metal can alter m6A modification by directly affecting catalytic activity and expression level of methyltransferases and demethylases, or through reactive oxygen species, eventually disrupting normal biological function and leading to diseases. Therefore, m6A RNA methylation may play a bridging role in heavy metal pollution-induced carcinogenesis. This review discusses interaction among heavy metal, m6A, and metal ions metabolism, and their regulatory mechanism, focuses on the role of m6A methylation and heavy metal pollution in cancer. Finally, the role of nutritional therapy that targeting m6A methylation to prevent metal ion metabolism disorder-induced cancer is summarized. [Display omitted] •M6A regulates RNA metabolisms and provides a new direction for therapy in cancers.•Heavy metal pollution can disrupt m6A modification to induce tumorigenesis.•Nutritional therapy that targeting m6A to prevent metal ion-induced cancer.
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Metal ions participate in nucleotide biosynthesis and repair, signal transduction, energy generation, immune defense, and other important metabolic processes. However, long-term environmental and occupational exposure to metals through food, air, soil, water, and industry can result in toxicity, serious health problems, and cancer. Recent evidence indicates dynamic and reversible m6A modification modulates various metal ion metabolism, such as iron absorption, calcium uptake and transport. In turn, environmental heavy metal can alter m6A modification by directly affecting catalytic activity and expression level of methyltransferases and demethylases, or through reactive oxygen species, eventually disrupting normal biological function and leading to diseases. Therefore, m6A RNA methylation may play a bridging role in heavy metal pollution-induced carcinogenesis. This review discusses interaction among heavy metal, m6A, and metal ions metabolism, and their regulatory mechanism, focuses on the role of m6A methylation and heavy metal pollution in cancer. Finally, the role of nutritional therapy that targeting m6A methylation to prevent metal ion metabolism disorder-induced cancer is summarized. 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source ScienceDirect Journals (5 years ago - present)
subjects air
biosynthesis
calcium
Cancers
carcinogenesis
catalytic activity
diet therapy
energy
gene expression
heavy metals
immune response
industry
iron absorption
Metal ions
methylation
methyltransferases
N6-methyladenine
Nutritional therapy
occupational exposure
pollution
reactive oxygen species
RNA
signal transduction
soil
toxicity
title The emerging role of N6-methyladenine RNA methylation in metal ion metabolism and metal-induced carcinogenesis
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