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赖氨酸甲基转移酶和精氨酸甲基转移酶在肾脏疾病中的作用及机制

The Role and Mechanism of Lysine Methyltransferase and Arginine Methyltransferase in Kidney Diseases.

作者信息

Zhou Xun, Chen Hui, Li Jinqing, Shi Yingfeng, Zhuang Shougang, Liu Na

机构信息

Department of Nephrology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.

Department of Medicine, Rhode Island Hospital and Alpert Medical School, Brown University, Providence, RI, United States.

出版信息

Front Pharmacol. 2022 Apr 26;13:885527. doi: 10.3389/fphar.2022.885527. eCollection 2022.

DOI:10.3389/fphar.2022.885527
PMID:35559246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9086358/
Abstract

Methylation can occur in both histones and non-histones. Key lysine and arginine methyltransferases under investigation for renal disease treatment include enhancer of zeste homolog 2 (EZH2), G9a, disruptor of telomeric silencing 1-like protein (DOT1L), and protein arginine methyltransferases (PRMT) 1 and 5. Recent studies have shown that methyltransferases expression and activity are also increased in several animal models of kidney injury, such as acute kidney injury(AKI), obstructive nephropathy, diabetic nephropathy and lupus nephritis. The inhibition of most methyltransferases can attenuate kidney injury, while the role of methyltransferase in different animal models remains controversial. In this article, we summarize the role and mechanism of lysine methyltransferase and arginine methyltransferase in various kidney diseases and highlight methyltransferase as a potential therapeutic target for kidney diseases.

摘要

甲基化可发生在组蛋白和非组蛋白中。正在研究用于肾脏疾病治疗的关键赖氨酸和精氨酸甲基转移酶包括zeste同源物2增强子(EZH2)、G9a、端粒沉默破坏因子1样蛋白(DOT1L)以及蛋白精氨酸甲基转移酶(PRMT)1和5。最近的研究表明,在几种肾脏损伤的动物模型中,如急性肾损伤(AKI)、梗阻性肾病、糖尿病肾病和狼疮性肾炎,甲基转移酶的表达和活性也会增加。大多数甲基转移酶的抑制可减轻肾脏损伤,而甲基转移酶在不同动物模型中的作用仍存在争议。在本文中,我们总结了赖氨酸甲基转移酶和精氨酸甲基转移酶在各种肾脏疾病中的作用和机制,并强调甲基转移酶作为肾脏疾病潜在治疗靶点的地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/6b5b06fbcab6/fphar-13-885527-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/d40b0ea77fef/fphar-13-885527-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/0b77bf356e09/fphar-13-885527-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/6b5b06fbcab6/fphar-13-885527-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/d40b0ea77fef/fphar-13-885527-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/0b77bf356e09/fphar-13-885527-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e599/9086358/6b5b06fbcab6/fphar-13-885527-g003.jpg

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本文引用的文献

1
Acute Kidney Injury: Biomarker-Guided Diagnosis and Management.急性肾损伤:生物标志物指导的诊断与管理。
Medicina (Kaunas). 2022 Feb 23;58(3):340. doi: 10.3390/medicina58030340.
2
Selective EZH2 inhibitor zld1039 alleviates inflammation in cisplatin-induced acute kidney injury partially by enhancing RKIP and suppressing NF-κB p65 pathway.选择性 EZH2 抑制剂 ZLD1039 通过增强 RKIP 和抑制 NF-κB p65 通路部分缓解顺铂诱导的急性肾损伤中的炎症。
Acta Pharmacol Sin. 2022 Aug;43(8):2067-2080. doi: 10.1038/s41401-021-00837-8. Epub 2021 Dec 22.
3
Synthesis and Biological Activity of a Cytostatic Inhibitor of MLLr Leukemia Targeting the DOT1L Protein.
DOT1L 在肾脏疾病中的新作用。
Mol Biol Rep. 2023 Jun;50(6):5415-5423. doi: 10.1007/s11033-023-08415-3. Epub 2023 Apr 22.
4
DOT1L promotes cell proliferation and invasion by epigenetically regulating STAT5B in renal cell carcinoma.DOT1L通过表观遗传调控肾细胞癌中的STAT5B促进细胞增殖和侵袭。
Am J Cancer Res. 2023 Jan 15;13(1):276-292. eCollection 2023.
5
microRNA-29b-3p attenuates diabetic nephropathy in mice by modifying EZH2.miRNA-29b-3p 通过调节 EZH2 减轻糖尿病肾病小鼠模型的肾脏损伤
Hormones (Athens). 2023 Jun;22(2):223-233. doi: 10.1007/s42000-022-00426-2. Epub 2023 Jan 24.
合成及具有细胞抑制活性的 DOT1L 蛋白靶向 MLLr 白血病抑制剂的生物学活性。
Molecules. 2021 Aug 31;26(17):5300. doi: 10.3390/molecules26175300.
4
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5
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Free Radic Biol Med. 2021 Aug 20;172:123-135. doi: 10.1016/j.freeradbiomed.2021.06.002. Epub 2021 Jun 5.
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Ann Palliat Med. 2021 Mar;10(3):3343-3353. doi: 10.21037/apm-21-417.
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Eur J Pharmacol. 2021 Jun 15;901:174097. doi: 10.1016/j.ejphar.2021.174097. Epub 2021 Apr 19.
10
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