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视黄酸与微小核糖核酸

Retinoic acid and microRNA.

作者信息

Wang Lijun, Rohatgi Atharva Piyush, Wan Yu-Jui Yvonne

机构信息

Department of Pathology and Laboratory Medicine, University of California Davis Health, Sacramento, CA, United States.

Department of Pathology and Laboratory Medicine, University of California Davis Health, Sacramento, CA, United States.

出版信息

Methods Enzymol. 2020;637:283-308. doi: 10.1016/bs.mie.2020.02.009. Epub 2020 Mar 28.

DOI:10.1016/bs.mie.2020.02.009
PMID:32359650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7445077/
Abstract

Retinoic acid (RA), the biologically active metabolite of vitamin A, regulates a vast spectrum of biological processes, such as cell differentiation, proliferation, apoptosis, and morphogenesis. microRNAs (miRNAs) play a crucial role in regulating gene expression by binding to messenger RNA (mRNA) which leads to mRNA degradation and/or translational repression. Like RA, miRNAs regulate multiple biological processes, including proliferation, differentiation, apoptosis, neurogenesis, tumorigenesis, and immunity. In fact, RA regulates the expression of many miRNAs to exert its biological functions. miRNA and RA regulatory networks have been studied in recent years. In this manuscript, we summarize literature that highlights the impact of miRNAs in RA-regulated molecular networks included in the PubMed.

摘要

视黄酸(RA)是维生素A的生物活性代谢产物,可调节广泛的生物过程,如细胞分化、增殖、凋亡和形态发生。微小RNA(miRNA)通过与信使核糖核酸(mRNA)结合来调节基因表达,从而导致mRNA降解和/或翻译抑制,在这一过程中发挥着关键作用。与RA一样,miRNA也调节多种生物过程,包括增殖、分化、凋亡、神经发生、肿瘤发生和免疫。事实上,RA通过调节许多miRNA的表达来发挥其生物学功能。近年来,miRNA和RA调控网络已得到研究。在本手稿中,我们总结了文献,这些文献突出了miRNA在PubMed中收录的RA调控分子网络中的影响。

相似文献

1
Retinoic acid and microRNA.视黄酸与微小核糖核酸
Methods Enzymol. 2020;637:283-308. doi: 10.1016/bs.mie.2020.02.009. Epub 2020 Mar 28.
2
RARs and microRNAs.视黄酸受体与微小核糖核酸
Subcell Biochem. 2014;70:151-79. doi: 10.1007/978-94-017-9050-5_8.
3
Retinoic acid differentially regulates retinoic acid receptor-mediated pathways in the Hep3B cell line.维甲酸对Hep3B细胞系中维甲酸受体介导的信号通路具有差异性调节作用。
Exp Cell Res. 1998 Jan 10;238(1):241-7. doi: 10.1006/excr.1997.3851.
4
Selective roles of retinoic acid receptor and retinoid x receptor in the suppression of apoptosis by all-trans-retinoic acid.视黄酸受体和类视黄醇X受体在全反式视黄酸抑制细胞凋亡中的选择性作用。
J Biol Chem. 2001 Apr 20;276(16):12697-701. doi: 10.1074/jbc.M011000200. Epub 2001 Jan 16.
5
Retinoic acid receptor gamma 2 gene expression is up-regulated by retinoic acid in 3T3-L1 preadipocytes.维甲酸受体γ2基因表达在3T3-L1前脂肪细胞中被维甲酸上调。
Biochem J. 1993 Aug 1;293 ( Pt 3)(Pt 3):807-12. doi: 10.1042/bj2930807.
6
Vitamin D3- and retinoic acid-induced monocytic differentiation: interactions between the endogenous vitamin D3 receptor, retinoic acid receptors, and retinoid X receptors in U-937 cells.维生素D3和视黄酸诱导的单核细胞分化:U-937细胞中内源性维生素D3受体、视黄酸受体和类视黄醇X受体之间的相互作用
Cell Growth Differ. 1996 Sep;7(9):1239-49.
7
Retinoic acid receptor and retinoid X receptor expression in retinoic acid-resistant human tumor cell lines.视黄酸受体和类视黄醇X受体在视黄酸耐药性人肿瘤细胞系中的表达
Mol Carcinog. 1993;8(2):112-22. doi: 10.1002/mc.2940080208.
8
Expression of nuclear retinoic acid receptor and retinoid X receptor mRNA in the cornea and conjunctiva.核视黄酸受体和视黄醇X受体mRNA在角膜和结膜中的表达。
Curr Eye Res. 1998 May;17(5):462-9. doi: 10.1076/ceyr.17.5.462.5189.
9
Regulation of retinoid-induced differentiation in embryonal carcinoma PCC4.aza1R cells: effects of retinoid-receptor selective ligands.维甲酸诱导胚胎癌PCC4.aza1R细胞分化的调控:维甲酸受体选择性配体的作用
Cell Growth Differ. 1996 Mar;7(3):327-37.
10
Synergistic activation of retinoic acid (RA)-responsive genes and induction of embryonal carcinoma cell differentiation by an RA receptor alpha (RAR alpha)-, RAR beta-, or RAR gamma-selective ligand in combination with a retinoid X receptor-specific ligand.视黄酸(RA)反应性基因的协同激活以及维甲酸受体α(RARα)、RARβ或RARγ选择性配体与视黄醇X受体特异性配体联合诱导胚胎癌细胞分化。
Mol Cell Biol. 1995 Dec;15(12):6481-7. doi: 10.1128/MCB.15.12.6481.

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SERPINA3 is expressed in human adipocytes and modulated by TNF-α and vitamin B6.丝氨酸蛋白酶抑制剂A3(SERPINA3)在人类脂肪细胞中表达,并受肿瘤坏死因子-α(TNF-α)和维生素B6调节。
In Vitro Cell Dev Biol Anim. 2025 May 27. doi: 10.1007/s11626-025-01053-y.
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Non-canonical retinoid signaling in neural development, regeneration and synaptic function.非经典类视黄醇信号在神经发育、再生及突触功能中的作用
Front Mol Neurosci. 2024 Mar 7;17:1371135. doi: 10.3389/fnmol.2024.1371135. eCollection 2024.
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The Beginning of Meiosis in Mammalian Female Germ Cells: A Never-Ending Story of Intrinsic and Extrinsic Factors.

本文引用的文献

1
inhibition reduces hepatic steatosis via FGF21 and FGFR1 induction.抑制作用通过诱导成纤维细胞生长因子21(FGF21)和成纤维细胞生长因子受体1(FGFR1)减轻肝脏脂肪变性。
JHEP Rep. 2020 Feb 18;2(2):100093. doi: 10.1016/j.jhepr.2020.100093. eCollection 2020 Apr.
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Regulation of cellular senescence by retinoid X receptors and their partners.视黄醇 X 受体及其伴侣对细胞衰老的调节。
Mech Ageing Dev. 2019 Oct;183:111131. doi: 10.1016/j.mad.2019.111131. Epub 2019 Aug 30.
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Rapamycin-upregulated miR-29b promotes mTORC1-hyperactive cell growth in TSC2-deficient cells by downregulating tumor suppressor retinoic acid receptor β (RARβ).
哺乳动物雌性生殖细胞减数分裂的起始:内在和外在因素的一个永无止境的故事。
Int J Mol Sci. 2022 Oct 20;23(20):12571. doi: 10.3390/ijms232012571.
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[Regulatory Effect of All-Trans Retinoic Acid on the Expression of IL-1β in Macrophages and the Mechanisms Involved].全反式维甲酸对巨噬细胞中白细胞介素-1β表达的调控作用及其相关机制
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5
Inhibition of RhoA and Cdc42 by miR-133a Modulates Retinoic Acid Signalling during Early Development of Posterior Cardiac Tube Segment.miR-133a 通过抑制 RhoA 和 Cdc42 调节心脏后段早期发育中的视黄酸信号。
Int J Mol Sci. 2022 Apr 10;23(8):4179. doi: 10.3390/ijms23084179.
6
Hepatocellular carcinoma immunotherapy: The impact of epigenetic drugs and the gut microbiome.肝细胞癌免疫疗法:表观遗传药物与肠道微生物群的影响
Liver Res. 2020 Dec;4(4):191-198. doi: 10.1016/j.livres.2020.10.001. Epub 2020 Oct 17.
雷帕霉素上调的 miR-29b 通过下调肿瘤抑制因子维甲酸受体 β(RARβ)促进 TSC2 缺陷细胞中 mTORC1 过度活跃的细胞生长。
Oncogene. 2019 Dec;38(49):7367-7383. doi: 10.1038/s41388-019-0957-5. Epub 2019 Aug 16.
4
The c-Myc-regulated miR-17-92 cluster mediates ATRA-induced APL cell differentiation.c-Myc调控的miR-17-92簇介导全反式维甲酸诱导的急性早幼粒细胞白血病细胞分化。
Asia Pac J Clin Oncol. 2019 Dec;15(6):364-370. doi: 10.1111/ajco.13225. Epub 2019 Jul 1.
5
Comprehensive study of nuclear receptor DNA binding provides a revised framework for understanding receptor specificity.对核受体 DNA 结合的综合研究为理解受体特异性提供了一个修正的框架。
Nat Commun. 2019 Jun 7;10(1):2514. doi: 10.1038/s41467-019-10264-3.
6
Retinoic acid receptor gamma is targeted by microRNA-124 and inhibits neurite outgrowth.视黄酸受体γ受 microRNA-124 靶向调控并抑制轴突生长。
Neuropharmacology. 2020 Feb;163:107657. doi: 10.1016/j.neuropharm.2019.05.034. Epub 2019 Jun 3.
7
Retinoic Acid Induces Differentiation of Mouse F9 Embryonic Carcinoma Cell by Modulating the miR-485 Targeting of Abhd2.视黄酸通过调节 Abhd2 的 miR-485 靶向作用诱导小鼠 F9 胚胎癌细胞分化。
Int J Mol Sci. 2019 Apr 26;20(9):2071. doi: 10.3390/ijms20092071.
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Alternative retinoid X receptor (RXR) ligands.替代视黄醇 X 受体 (RXR) 配体。
Mol Cell Endocrinol. 2019 Jul 1;491:110436. doi: 10.1016/j.mce.2019.04.016. Epub 2019 Apr 23.
9
RAS-Responsive Element-Binding Protein 1 Blocks the Granulocytic Differentiation of Myeloid Leukemia Cells.RAS 反应元件结合蛋白 1 阻止髓系白血病细胞的粒细胞分化。
Oncol Res. 2019 Jul 12;27(7):809-818. doi: 10.3727/096504018X15451301487729. Epub 2019 Apr 8.
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Small molecules for fat combustion: targeting obesity.用于脂肪燃烧的小分子:针对肥胖症
Acta Pharm Sin B. 2019 Mar;9(2):220-236. doi: 10.1016/j.apsb.2018.09.007. Epub 2018 Sep 19.