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川崎病中表观遗传低甲基化与基质金属蛋白酶9的上调

Epigenetic hypomethylation and upregulation of matrix metalloproteinase 9 in Kawasaki disease.

作者信息

Kuo Ho-Chang, Li Sung-Chou, Huang Lien-Hung, Huang Ying-Hsien

机构信息

Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, Taiwan.

Kawasaki Disease Center, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.

出版信息

Oncotarget. 2017 Jul 28;8(37):60875-60891. doi: 10.18632/oncotarget.19650. eCollection 2017 Sep 22.


DOI:10.18632/oncotarget.19650
PMID:28977831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5617391/
Abstract

BACKGROUND: Kawasaki disease (KD) is a type of febrile coronary vasculitis occurring in children. Some researchers have suggested that changes in genetic signatures, such as matrix metalloproteinases (MMPs), are critical markers for cardiovascular diseases. This study aims to provide a comprehensive survey of global DNA methylation levels and MMP transcripts of KD patients compared to control subjects. MATERIALS AND METHODS: For chips studies, we recruited a total of 18 KD patients, prior to receiving intravenous immunoglobulin (IVIG) and at least 3 weeks after IVIG treatment, as well as 18 healthy and 18 febrile control subjects. We applied Illumina HumanMethylation450 BeadChip and Affymetrix GeneChip® Human Transcriptome Array 2.0 to evaluate their CpG markers and expression levels, respectively. Then we used a separate cohort to carry out real-time quantitative PCR validations of mRNA levels. RESULTS: The expressions of mRNA levels of MMP-8, -9, and -25 were significantly upregulated in KD patients compared to the healthy and febrile controls. Once KD patients underwent IVIG treatment, these MMPs considerably decreased. In particular, the methylation status of CpG sites of MMP-9 indicated a significant opposite tendency between both stages of not only the KD samples but also the controls. We also observed the mRNA level of MMP-9 to be higher in KD patients with coronary arterial lesion formation. CONCLUSION: This study is the first to report epigenetic hypomethylation, an increased MMP-9 transcript, and the upregulation of MMP-9 in KD patients who had formed coronary arterial lesions.

摘要

背景:川崎病(KD)是一种发生于儿童的发热性冠状动脉血管炎。一些研究人员认为,基因特征的变化,如基质金属蛋白酶(MMPs),是心血管疾病的关键标志物。本研究旨在全面调查KD患者与对照受试者相比的全球DNA甲基化水平和MMP转录本。 材料与方法:对于芯片研究,我们共招募了18例KD患者,分别在接受静脉注射免疫球蛋白(IVIG)之前和IVIG治疗后至少3周,以及18例健康对照和18例发热对照受试者。我们分别应用Illumina HumanMethylation450 BeadChip和Affymetrix GeneChip® Human Transcriptome Array 2.0来评估他们的CpG标记和表达水平。然后我们使用一个独立的队列对mRNA水平进行实时定量PCR验证。 结果:与健康对照和发热对照相比,KD患者中MMP-8、-9和-25的mRNA水平表达显著上调。一旦KD患者接受IVIG治疗,这些MMPs显著下降。特别是,MMP-9的CpG位点甲基化状态在KD样本和对照的两个阶段均呈现出显著相反的趋势。我们还观察到,在有冠状动脉病变形成的KD患者中,MMP-9的mRNA水平更高。 结论:本研究首次报道了KD患者中表观遗传低甲基化、MMP-9转录本增加以及MMP-9在形成冠状动脉病变的KD患者中的上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/6c44e3ca62b9/oncotarget-08-60875-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/294d42c98588/oncotarget-08-60875-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/063a98000744/oncotarget-08-60875-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/a86fa1a1ceb1/oncotarget-08-60875-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/6c44e3ca62b9/oncotarget-08-60875-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/294d42c98588/oncotarget-08-60875-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/063a98000744/oncotarget-08-60875-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/a86fa1a1ceb1/oncotarget-08-60875-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e563/5617391/6c44e3ca62b9/oncotarget-08-60875-g004.jpg

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BMC Infect Dis. 2024-7-3

[2]
NLRC4 methylation and its response to intravenous immunoglobulin therapy in Kawasaki disease: a case control study.

BMC Pediatr. 2024-3-16

[3]
Association between gene polymorphisms and coronary artery lesion in Kawasaki disease.

Front Med (Lausanne). 2023-7-27

[4]
DNA methylation and cardiovascular disease in humans: a systematic review and database of known CpG methylation sites.

Clin Epigenetics. 2023-3-30

[5]
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Front Immunol. 2022

[6]
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Evid Based Complement Alternat Med. 2022-9-14

[7]
KDmarkers: A biomarker database for investigating epigenetic methylation and gene expression levels in Kawasaki disease.

Comput Struct Biotechnol J. 2022-3-10

[8]
Correlation Between Matrix Metalloproteinases With Coronary Artery Lesion Caused by Kawasaki Disease.

Front Pediatr. 2022-2-11

[9]
Intravenous Immunoglobulin Therapy Restores the Quantity and Phenotype of Circulating Dendritic Cells and CD4 T Cells in Children With Acute Kawasaki Disease.

Front Immunol. 2022

[10]
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本文引用的文献

[1]
Association of Matrix Metalloproteinase Levels with Collagen Degradation in the Context of Abdominal Aortic Aneurysm.

Eur J Vasc Endovasc Surg. 2017-4

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MicroRNA-29a Alleviates Bile Duct Ligation Exacerbation of Hepatic Fibrosis in Mice through Epigenetic Control of Methyltransferases.

Int J Mol Sci. 2017-1-18

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Identifying genetic hypomethylation and upregulation of Toll-like receptors in Kawasaki disease.

Oncotarget. 2017-2-14

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PLoS One. 2016-6-30

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J Immunol. 2016-7-1

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Interferon-gamma Genetic Polymorphism and Expression in Kawasaki Disease.

Medicine (Baltimore). 2016-4

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