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砷甲基化相关的 miRNA 和 mRNA 表达。

Relative miRNA and mRNA expression involved in arsenic methylation.

机构信息

Department of Occupational Health, Yunnan Provincial Center for Disease Control and Prevention, Kunming, Yunnan, China.

First Affiliated Hospital of Kunming Medical University, Kunming, People's Republic of China.

出版信息

PLoS One. 2018 Dec 13;13(12):e0209014. doi: 10.1371/journal.pone.0209014. eCollection 2018.

DOI:10.1371/journal.pone.0209014
PMID:30543710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6292570/
Abstract

Three arsenic species in urine are measured using an atomic absorption spectrophotometer. RT-PCR is performed to detect the expression levels of AS3MT, 3 miRNAs, and 17 relative mRNAs in 43 workers producing arsenic trioxide, 36 workers who stopped exposure to arsenic for 85 days, and 24 individuals as the control group. The concentrations of urinary arsenic are very high in workers. A negative correlation between AS3MT and MiR-548c-3p is found. There exist significant changes for most selected miRNAs and mRNAs in workers. There are no significant differences between workers who stopped exposure to arsenic and the control group for most miRNAs and mRNAs, but the MiR-548c-3p levels show significant changes. Similar positive correlations between the expression of AS3MT and all selected mRNAs are found. Negative correlations between the expression of MiR-548c-3p and many relative mRNAs are found as well. AS3MT and MiR-548c-3p may regulate arsenic methylation jointly, which when involved in a group of relative mRNAs may play roles in arsenic metabolism and epigenetic changes caused by this metabolism.

摘要

采用原子吸收分光光度计测定尿中三种砷形态。采用 RT-PCR 检测 43 名生产三氧化二砷工人、36 名停止砷暴露 85 天工人和 24 名对照组个体中 AS3MT、3 种 miRNA 和 17 种相对 mRNA 的表达水平。工人尿砷浓度非常高。发现 AS3MT 与 MiR-548c-3p 呈负相关。大多数选定的 miRNA 和 mRNA 在工人中存在显著变化。大多数 miRNA 和 mRNA 在停止砷暴露的工人和对照组之间没有显著差异,但 MiR-548c-3p 水平显示出显著变化。AS3MT 的表达与所有选定的 mRNA 之间存在相似的正相关。MiR-548c-3p 的表达与许多相对 mRNA 之间存在负相关。AS3MT 和 MiR-548c-3p 可能共同调节砷甲基化,当涉及一组相对 mRNA 时,它们可能在砷代谢和这种代谢引起的表观遗传变化中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/310f/6292570/1780d38e99c6/pone.0209014.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/310f/6292570/cb043acd7bea/pone.0209014.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/310f/6292570/1780d38e99c6/pone.0209014.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/310f/6292570/cb043acd7bea/pone.0209014.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/310f/6292570/1780d38e99c6/pone.0209014.g004.jpg

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本文引用的文献

1
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Biomed Pharmacother. 2015 Oct;75:111-6. doi: 10.1016/j.biopha.2015.07.027. Epub 2015 Aug 18.
2
Arsenic responsive microRNAs in vivo and their potential involvement in arsenic-induced oxidative stress.体内砷反应性微小RNA及其在砷诱导的氧化应激中的潜在作用。
Toxicol Appl Pharmacol. 2015 Mar 15;283(3):198-209. doi: 10.1016/j.taap.2015.01.014. Epub 2015 Jan 24.
3
MicroRNA biogenesis pathway from the salmon louse (Caligus rogercresseyi): emerging role in delousing drug response.
砷 (+3 氧化态) 甲基转移酶 (AS3MT) 中的多态性可预测接受 AsO 治疗的 APL 患者发生高白细胞血症和砷代谢的情况。
Arch Toxicol. 2020 Apr;94(4):1203-1213. doi: 10.1007/s00204-020-02686-6. Epub 2020 Feb 28.
4
The Promises and Challenges of Toxico-Epigenomics: Environmental Chemicals and Their Impacts on the Epigenome.毒理 - 表观基因组学的前景与挑战:环境化学物质及其对表观基因组的影响。
Environ Health Perspect. 2020 Jan;128(1):15001. doi: 10.1289/EHP6104. Epub 2020 Jan 17.
来自海虱(Caligus rogercresseyi)的微小RNA生物合成途径:在灭虱药物反应中的新作用。
Gene. 2015 Jan 25;555(2):231-41. doi: 10.1016/j.gene.2014.11.008. Epub 2014 Nov 7.
4
miRNAs in pancreatic cancer: therapeutic potential, delivery challenges and strategies.miRNAs 在胰腺癌中的作用:治疗潜力、递药挑战和策略。
Adv Drug Deliv Rev. 2015 Jan;81:34-52. doi: 10.1016/j.addr.2014.09.006. Epub 2014 Sep 22.
5
AS3MT, GSTO, and PNP polymorphisms: impact on arsenic methylation and implications for disease susceptibility.AS3MT、GSTO 和 PNP 多态性:对砷甲基化的影响及其对疾病易感性的影响。
Environ Res. 2014 Jul;132:156-67. doi: 10.1016/j.envres.2014.03.012. Epub 2014 May 8.
6
Arsenic exposure triggers a shift in microRNA expression.砷暴露会引发 microRNA 表达谱的改变。
Sci Total Environ. 2014 Feb 15;472:672-80. doi: 10.1016/j.scitotenv.2013.11.092. Epub 2013 Dec 7.
7
Comparison of genome-wide DNA methylation in urothelial carcinomas of patients with and without arsenic exposure.比较有和无砷暴露的膀胱癌患者全基因组 DNA 甲基化。
Environ Res. 2014 Jan;128:57-63. doi: 10.1016/j.envres.2013.10.006. Epub 2013 Nov 22.
8
Deregulation of cancer-related miRNAs is a common event in both benign and malignant human breast tumors.癌症相关 miRNAs 的失调是良性和恶性人类乳腺肿瘤中的常见事件。
Carcinogenesis. 2014 Jan;35(1):76-85. doi: 10.1093/carcin/bgt333. Epub 2013 Oct 8.
9
LIN28/LIN28B: an emerging oncogenic driver in cancer stem cells.LIN28/LIN28B:癌症干细胞中的新兴致癌驱动因子。
Int J Biochem Cell Biol. 2013 May;45(5):973-8. doi: 10.1016/j.biocel.2013.02.006. Epub 2013 Feb 16.
10
Methylation capacity of arsenic and skin lesions in smelter plant workers.砷的甲基化能力与冶炼厂工人的皮肤损伤。
Environ Toxicol Pharmacol. 2012 Sep;34(2):624-630. doi: 10.1016/j.etap.2012.07.003. Epub 2012 Jul 21.