A Functional Variant of CYP4V2 Contributes to Asthma Susceptibility Through Methylation-Mediated Regulation of the Arachidonic Acid Pathway.

IF 3.3 3区 医学 Q2 ALLERGY
Journal of Asthma and Allergy Pub Date : 2026-07-27 eCollection Date: 2026-01-01 DOI:10.2147/JAA.S598881
Xiangran Chen, Terence Yin Weng Lam, Yang Yie Sio, Yee-How Say, Kavita Reginald, Fook Tim Chew
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引用次数: 0

Abstract

Background: CYP4V2 is involved in lipid metabolism, but its contribution to asthma is poorly understood. This study aimed to investigate genetic polymorphisms and regulatory features of CYP4V2 in asthma development.

Methods: We performed an integrative multi-omics analysis combining transcriptomic, genetic, and epigenetic data from peripheral blood mononuclear cells (PBMCs) of individuals in the Singapore/Malaysia Cross-Sectional Genetics and Epidemiological Study (SMCSGES) cohort. The influence of CYP4V2 expression on asthma risk and expression of genes involved in arachidonic acid (AA) pathway were evaluated, followed by expression quantitative trait locus (eQTL) analysis to identify regulatory variants. DNA methylation analyses were conducted to assess epigenetic regulation of CYP4V2, and promoter reporter assays were used to functionally validate candidate regulatory CpG sites.

Results: The upregulation of CYP4V2 in PBMCs was associated with an increased risk of asthma and inversely associated with PTGER2 and ALOX5AP in the AA pathway. The SNP rs2276921 was identified as the only expression quantitative trait locus (eQTL) associated with both increased CYP4V2 expression and asthma risk (FDR-adjusted p < 0.05; OR = 1.24, 95% CI = 1.10-1.40). The minor allele G of rs2276921 was associated with low methylation at cg23232844 (p = 3.94 × 10-3) and cg11969330 (p = 4.25 × 10-2), located in the promoters of the protein-coding and non-coding CYP4V2 isoforms respectively. Promoter assays indicated that these two CpG sites inhibited CYP4V2 expression, supporting the regulatory effect of rs2276921 on CYP4V2 expression may be mediated through methylation.

Conclusion: This study identified rs2276921 and CpG sites cg23232844 and cg11969330 that regulate CYP4V2 expression. CYP4V2 potentially modulates the AA metabolism and contributes to asthma susceptibility. These findings suggest CYP4V2 as a potential biomarker and therapeutic target in asthma.

CYP4V2的功能变异通过甲基化介导的花生四烯酸途径调节哮喘易感性
背景:CYP4V2参与脂质代谢,但其在哮喘中的作用尚不清楚。本研究旨在探讨CYP4V2在哮喘发生中的遗传多态性和调控特征。方法:我们对新加坡/马来西亚横断面遗传学和流行病学研究(SMCSGES)队列中个体的外周血单个核细胞(PBMCs)进行了综合多组学分析,结合了转录组学、遗传学和表观遗传学数据。评估CYP4V2表达对哮喘风险及花生四烯酸(AA)通路相关基因表达的影响,并通过表达数量性状位点(eQTL)分析鉴定调节变异。DNA甲基化分析用于评估CYP4V2的表观遗传调控,启动子报告基因检测用于功能验证候选CpG调控位点。结果:pbmc中CYP4V2的上调与哮喘风险增加相关,与AA通路中的PTGER2和ALOX5AP呈负相关。SNP rs2276921被确定为唯一与CYP4V2表达增加和哮喘风险相关的表达数量性状位点(eQTL)(经fdr校正p < 0.05; OR = 1.24, 95% CI = 1.10-1.40)。rs2276921的次要等位基因G与位于CYP4V2蛋白编码和非编码亚型启动子上的cg23232844 (p = 3.94 × 10-3)和cg11969330 (p = 4.25 × 10-2)的低甲基化相关。启动子实验表明,这两个CpG位点抑制CYP4V2表达,支持rs2276921对CYP4V2表达的调控作用可能是通过甲基化介导的。结论:本研究确定了调控CYP4V2表达的rs2276921和CpG位点cg23232844和cg11969330。CYP4V2可能调节AA代谢并有助于哮喘易感性。这些发现表明CYP4V2是哮喘的潜在生物标志物和治疗靶点。
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来源期刊
Journal of Asthma and Allergy
Journal of Asthma and Allergy Medicine-Immunology and Allergy
CiteScore
5.30
自引率
6.20%
发文量
185
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal publishing original research, reports, editorials and commentaries on the following topics: Asthma; Pulmonary physiology; Asthma related clinical health; Clinical immunology and the immunological basis of disease; Pharmacological interventions and new therapies. Although the main focus of the journal will be to publish research and clinical results in humans, preclinical, animal and in vitro studies will be published where they shed light on disease processes and potential new therapies.
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