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SIRT1 在酒精性肝病中的新兴作用。

Emerging Roles of SIRT1 in Alcoholic Liver Disease.

机构信息

Department of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, China.

School of Pharmacy, Institute of Liver Diseases, Anhui Medical University, Hefei 230032, Anhui, China.

出版信息

Int J Biol Sci. 2020 Oct 17;16(16):3174-3183. doi: 10.7150/ijbs.49535. eCollection 2020.


DOI:10.7150/ijbs.49535
PMID:33162823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7645991/
Abstract

Alcoholic liver disease (ALD) is the most prevalent type of chronic liver disease worldwide with a wide spectrum of liver pathologies ranging from simple steatosis to steatohepatitis, cirrhosis, and even hepatocellular carcinoma. It has been demonstrated that ALD is mediated in whole or in part by a central signaling molecule sirtuin 1 (SIRT1), a conserved class III histone deacetylase.SIRT1 plays beneficial roles in regulating hepatic lipid metabolism, inhibiting hepatic inflammation, controlling hepatic fibrosis and mediating hepatocellular carcinoma in ALD. However, underlying molecular mechanisms are complex and remain incompletely understood. The aim of this review was to highlight the latest advances in understanding of SIRT1 regulatory mechanisms in ALD and discuss their unique potential role as novel therapeutic target for ALD treatment.

摘要

酒精性肝病(ALD)是全球最常见的慢性肝病,其肝脏病理变化广泛,从单纯性脂肪变性到脂肪性肝炎、肝硬化,甚至肝细胞癌。已经证明,ALD 是由一种中央信号分子沉默调节蛋白 1(SIRT1)介导的,它是一种保守的 III 类组蛋白去乙酰化酶。SIRT1 在调节肝脏脂质代谢、抑制肝脏炎症、控制肝纤维化和介导 ALD 中的肝细胞癌方面发挥有益作用。然而,潜在的分子机制很复杂,仍不完全清楚。本综述的目的是强调 SIRT1 在 ALD 中的调节机制的最新研究进展,并讨论其作为 ALD 治疗的新型治疗靶点的独特潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/9036da10cb05/ijbsv16p3174g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/179585b81e60/ijbsv16p3174g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/f0c1e8e527c4/ijbsv16p3174g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/9036da10cb05/ijbsv16p3174g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/179585b81e60/ijbsv16p3174g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/f0c1e8e527c4/ijbsv16p3174g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fad/7645991/9036da10cb05/ijbsv16p3174g003.jpg

相似文献

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Emerging Roles of SIRT1 in Alcoholic Liver Disease.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
The mechanism of dysbiosis in alcoholic liver disease leading to liver cancer.

Hepatoma Res. 2020

[2]
Relevance of SIRT1-NF-κB Axis as Therapeutic Target to Ameliorate Inflammation in Liver Disease.

Int J Mol Sci. 2020-5-29

[3]
Sirtuin 1: A Dilemma in Transplantation.

J Transplant. 2020-4-25

[4]
Molecular mechanisms of ethanol biotransformation: enzymes of oxidative and nonoxidative metabolic pathways in human.

Xenobiotica. 2020-10

[5]
Clinical presentation of alcoholic liver disease and non-alcoholic fatty liver disease: spectrum and diagnosis.

Transl Gastroenterol Hepatol. 2020-4-5

[6]
PPARs as Metabolic Regulators in the Liver: Lessons from Liver-Specific PPAR-Null Mice.

Int J Mol Sci. 2020-3-17

[7]
Resveratrol protects against ethanol-induced impairment of insulin secretion in INS-1 cells through SIRT1-UCP2 axis.

Toxicol In Vitro. 2020-2-20

[8]
Aging exacerbates high-fat diet-induced steatohepatitis through alteration in hepatic lipid metabolism in mice.

J Gastroenterol Hepatol. 2020-2-17

[9]
Blockade of the NLRP3 inflammasome improves metabolic health and lifespan in obese mice.

Geroscience. 2020-4

[10]
Cryptotanshinone from the Bunge Attenuates Ethanol-Induced Liver Injury by Activation of AMPK/SIRT1 and Nrf2 Signaling Pathways.

Int J Mol Sci. 2019-12-30

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