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白癜风中的表观遗传修饰

Epigenetic Modifications in Vitiligo.

作者信息

Huang Xin, Zhu Jing, Wei Tianqi, Luo Lingling, Li Chengrang, Zhao Ming

机构信息

Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, Jiangsu, China.

出版信息

Clin Rev Allergy Immunol. 2025 Apr 9;68(1):39. doi: 10.1007/s12016-025-09048-z.

DOI:10.1007/s12016-025-09048-z
PMID:40205284
Abstract

Vitiligo is an autoimmune depigmenting skin disorder and can affect the mental health of the patients. Current research suggests that the development of vitiligo involves a combination of genetic susceptibility, immune imbalance, and oxidative stress. However, its pathogenesis has not been fully elucidated. Epigenetic modification has gained increasing attention as an emerging way to regulate gene expression at the transcriptional or post-transcriptional level. Currently known modes of epigenetic modification include the regulation of non-coding RNAs, DNA methylation, and histone modification. Studies suggest they play important roles in tumors, immune disorders, and inflammatory diseases. In recent years, the value of epigenetics in the diagnosis, treatment, and prognosis of vitiligo has been explored. They showed the potential to serve as biomarkers and play a therapeutic role. In this review, we summarize the epigenetic modification mechanisms involved in the pathogenesis of vitiligo, including physiological processes such as immune homeostasis, melanocyte survival, cell adhesion and migration, and metabolism. This will help us fully understand the progress of epigenetic research in vitiligo and lay the foundation for targeted therapeutic-related research.

摘要

白癜风是一种自身免疫性色素脱失性皮肤病,会影响患者的心理健康。目前的研究表明,白癜风的发病涉及遗传易感性、免疫失衡和氧化应激等多种因素。然而,其发病机制尚未完全阐明。表观遗传修饰作为一种在转录或转录后水平调节基因表达的新兴方式,越来越受到关注。目前已知的表观遗传修饰模式包括非编码RNA的调控、DNA甲基化和组蛋白修饰。研究表明,它们在肿瘤、免疫紊乱和炎症性疾病中发挥重要作用。近年来,表观遗传学在白癜风的诊断、治疗和预后方面的价值已得到探索。它们显示出作为生物标志物的潜力并发挥治疗作用。在这篇综述中,我们总结了白癜风发病机制中涉及的表观遗传修饰机制,包括免疫稳态、黑素细胞存活、细胞黏附与迁移以及代谢等生理过程。这将有助于我们全面了解白癜风表观遗传研究的进展,并为靶向治疗相关研究奠定基础。

相似文献

1
Epigenetic Modifications in Vitiligo.白癜风中的表观遗传修饰
Clin Rev Allergy Immunol. 2025 Apr 9;68(1):39. doi: 10.1007/s12016-025-09048-z.
2
Genetics and epigenetics in vitiligo.白癜风的遗传学与表观遗传学
J Dermatol Sci. 2025 Mar;117(3):45-51. doi: 10.1016/j.jdermsci.2025.01.004. Epub 2025 Jan 22.
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Transcriptome and Differential Methylation Integration Analysis Identified Important Differential Methylation Annotation Genes and Functional Epigenetic Modules Related to Vitiligo.转录组与差异甲基化整合分析鉴定出与白癜风相关的重要差异甲基化注释基因和功能性表观遗传模块。
Front Immunol. 2021 Mar 10;12:587440. doi: 10.3389/fimmu.2021.587440. eCollection 2021.
4
Vitiligo: Focus on Clinical Aspects, Immunopathogenesis, and Therapy.白癜风:关注临床方面、免疫发病机制和治疗。
Clin Rev Allergy Immunol. 2018 Feb;54(1):52-67. doi: 10.1007/s12016-017-8622-7.
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Critical Link Between Epigenetics and Transcription Factors in the Induction of Autoimmunity: a Comprehensive Review.自身免疫诱导中表观遗传学与转录因子之间的关键联系:综述
Clin Rev Allergy Immunol. 2016 Jun;50(3):333-44. doi: 10.1007/s12016-016-8534-y.
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Current insight into the roles of microRNA in vitiligo.当前对 microRNA 在白癜风中作用的认识。
Mol Biol Rep. 2020 Apr;47(4):3211-3219. doi: 10.1007/s11033-020-05336-3. Epub 2020 Feb 21.
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Autoimmunity in vitiligo: Therapeutic implications and opportunities.白癜风中的自身免疫:治疗意义与机遇
Autoimmun Rev. 2022 Jan;21(1):102932. doi: 10.1016/j.autrev.2021.102932. Epub 2021 Sep 11.
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[Epigenetics' implication in autism spectrum disorders: A review].[表观遗传学在自闭症谱系障碍中的影响:综述]
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Frontiers and controversies in the pathobiology of vitiligo: separating the wheat from the chaff.白癜风病理生物学的前沿与争议:去伪存真
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本文引用的文献

1
Role of miR-16, 146a, 19b and 720 gene expressions in the pathogenesis and diagnosis of vitiligo.miR-16、146a、19b和720基因表达在白癜风发病机制及诊断中的作用
Sci Rep. 2025 Jan 6;15(1):1031. doi: 10.1038/s41598-024-83489-y.
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FOXO3 induces TUG1-mediated miR-375/GATA3 signaling axis to promote the survival of melanocytes in vitiligo.FOXO3 诱导 TUG1 介导的 miR-375/GATA3 信号轴促进白癜风黑素细胞的存活。
FASEB J. 2024 Nov 15;38(21):e70145. doi: 10.1096/fj.202400676RR.
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Histone modification in psoriasis: Molecular mechanisms and potential therapeutic targets.
银屑病中的组蛋白修饰:分子机制与潜在治疗靶点。
Exp Dermatol. 2024 Aug;33(8):e15151. doi: 10.1111/exd.15151.
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Disorganisation of basement membrane zone architecture impairs melanocyte residence in vitiligo.基底膜带结构的紊乱会损害白癜风中黑素细胞的定居。
J Pathol. 2024 Sep;264(1):30-41. doi: 10.1002/path.6321. Epub 2024 Jul 11.
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3D-hUMSCs Exosomes Ameliorate Vitiligo by Simultaneously Potentiating Treg Cells-Mediated Immunosuppression and Suppressing Oxidative Stress-Induced Melanocyte Damage.3D-hUMSC 细胞外囊泡通过同时增强 Treg 细胞介导的免疫抑制和抑制氧化应激诱导的黑素细胞损伤来改善白癜风。
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Oxidative stress-induced hypermethylation and low expression of ANXA2R: Novel insights into the dysfunction of melanocytes in vitiligo.氧化应激诱导的 ANXA2R 高甲基化和低表达:白癜风黑素细胞功能障碍的新见解。
J Dermatol Sci. 2024 Jun;114(3):115-123. doi: 10.1016/j.jdermsci.2024.02.009. Epub 2024 Feb 29.
7
Vitiligo: advances in pathophysiology research and treatment development.白癜风:病理生理学研究和治疗开发的进展。
Trends Mol Med. 2024 Sep;30(9):844-862. doi: 10.1016/j.molmed.2024.04.009. Epub 2024 May 4.
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Interleukin-2 signaling in the regulation of T cell biology in autoimmunity and cancer.白细胞介素-2 信号在自身免疫和癌症中 T 细胞生物学的调节作用。
Immunity. 2024 Mar 12;57(3):414-428. doi: 10.1016/j.immuni.2024.02.001.
9
Exosomes containing miR-1469 regulate natural killer cells by targeting CD122 in non-segmental vitiligo.含有miR-1469的外泌体通过靶向非节段性白癜风中的CD122来调节自然杀伤细胞。
J Dermatol Sci. 2024 Feb;113(2):42-50. doi: 10.1016/j.jdermsci.2023.12.006. Epub 2023 Dec 24.
10
Genome-wide DNA methylation of lesional and peri-lesional skin in vitiligo: a comparative and integrated analysis of multi-omics in Chinese population.白癜风皮损和皮损周围皮肤的全基因组 DNA 甲基化:中国人群多组学的比较和综合分析。
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