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cg11702988 位点的 DNA 甲基化是囊性纤维化肺部疾病严重程度的生物标志物:一项纵向研究。

DNA Methylation at cg11702988 Is a Biomarker of Lung Disease Severity in Cystic Fibrosis: A Longitudinal Study.

机构信息

LGMR, EA7402 University of Montpellier, 34093 Montpellier, France.

CRCM, CHU Montpellier, 34090 Montpellier, France.

出版信息

Genes (Basel). 2021 Mar 19;12(3):441. doi: 10.3390/genes12030441.

DOI:10.3390/genes12030441
PMID:33808877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8003783/
Abstract

Cystic fibrosis (CF) is a chronic genetic disease that mainly affects the respiratory and gastrointestinal systems. No curative treatments are available, but the follow-up in specialized centers has greatly improved the patient life expectancy. Robust biomarkers are required to monitor the disease, guide treatments, stratify patients, and provide outcome measures in clinical trials. In the present study, we outline a strategy to select putative DNA methylation biomarkers of lung disease severity in cystic fibrosis patients. In the discovery step, we selected seven potential biomarkers using a genome-wide DNA methylation dataset that we generated in nasal epithelial samples from the MethylCF cohort. In the replication step, we assessed the same biomarkers using sputum cell samples from the MethylBiomark cohort. Of interest, DNA methylation at the cg11702988 site ( gene) positively correlated with lung function and BMI, and negatively correlated with lung disease severity, chronic infection, and the number of exacerbations. These results were replicated in prospective sputum samples collected at four time points within an 18-month period and longitudinally. To conclude, (i) we identified a DNA methylation biomarker that correlates with CF severity, (ii) we provided a method to easily assess this biomarker, and (iii) we carried out the first longitudinal analysis of DNA methylation in CF patients. This new epigenetic biomarker could be used to stratify CF patients in clinical trials.

摘要

囊性纤维化 (CF) 是一种慢性遗传疾病,主要影响呼吸系统和胃肠道系统。目前尚无治愈方法,但在专门中心的随访大大提高了患者的预期寿命。需要强有力的生物标志物来监测疾病、指导治疗、对患者进行分层,并提供临床试验的结果衡量标准。在本研究中,我们概述了一种选择囊性纤维化患者肺部疾病严重程度的潜在 DNA 甲基化生物标志物的策略。在发现步骤中,我们使用我们在 MethylCF 队列的鼻腔上皮样本中生成的全基因组 DNA 甲基化数据集选择了七个潜在的生物标志物。在复制步骤中,我们使用来自 MethylBiomark 队列的痰细胞样本评估了相同的生物标志物。有趣的是,cg11702988 位点 (基因) 的 DNA 甲基化与肺功能和 BMI 呈正相关,与肺部疾病严重程度、慢性感染和恶化次数呈负相关。这些结果在 18 个月内的四个时间点收集的前瞻性痰样本中得到了复制,并进行了纵向分析。总之,(i) 我们确定了一个与 CF 严重程度相关的 DNA 甲基化生物标志物,(ii) 我们提供了一种简单评估该生物标志物的方法,(iii) 我们进行了 CF 患者中 DNA 甲基化的首次纵向分析。这种新的表观遗传生物标志物可用于临床试验中对 CF 患者进行分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/78ef5bd19e8e/genes-12-00441-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/27ec92bb9414/genes-12-00441-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/93c13c826b28/genes-12-00441-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/a47a6ad7caef/genes-12-00441-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/78ef5bd19e8e/genes-12-00441-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/27ec92bb9414/genes-12-00441-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/93c13c826b28/genes-12-00441-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/a47a6ad7caef/genes-12-00441-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/093c/8003783/78ef5bd19e8e/genes-12-00441-g004.jpg

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本文引用的文献

1
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J Cyst Fibros. 2020 Sep;19(5):677-687. doi: 10.1016/j.jcf.2020.05.011. Epub 2020 Jun 7.
2
Laboratory biomarkers for lung disease severity and progression in cystic fibrosis.用于评估囊性纤维化肺病严重程度和进展的实验室生物标志物。
Clin Chim Acta. 2020 Sep;508:277-286. doi: 10.1016/j.cca.2020.05.015. Epub 2020 May 16.
3
Blood co-expression modules identify potential modifier genes of diabetes and lung function in cystic fibrosis.
成纤维细胞表型的 DNA 甲基化及其对肺纤维化的贡献。
Cells. 2021 Aug 3;10(8):1977. doi: 10.3390/cells10081977.
血液共表达模块鉴定囊性纤维化中糖尿病和肺功能的潜在修饰基因。
PLoS One. 2020 Apr 17;15(4):e0231285. doi: 10.1371/journal.pone.0231285. eCollection 2020.
4
DNA methylation changes in cystic fibrosis: Cause or consequence?囊性纤维化中的 DNA 甲基化变化:是原因还是结果?
Clin Genet. 2020 Jul;98(1):3-9. doi: 10.1111/cge.13731. Epub 2020 Mar 12.
5
CFTR structure, stability, function and regulation.CFTR 结构、稳定性、功能和调节。
Biol Chem. 2019 Sep 25;400(10):1359-1370. doi: 10.1515/hsz-2018-0470.
6
Genome-wide DNA methylation profiling shows a distinct epigenetic signature associated with lung macrophages in cystic fibrosis.全基因组 DNA 甲基化分析显示,囊性纤维化肺巨噬细胞存在独特的表观遗传特征。
Clin Epigenetics. 2018 Dec 10;10(1):152. doi: 10.1186/s13148-018-0580-2.
7
Phospholipid flippases enable precursor B cells to flee engulfment by macrophages.磷脂翻转酶使前体 B 细胞能够逃避巨噬细胞的吞噬。
Proc Natl Acad Sci U S A. 2018 Nov 27;115(48):12212-12217. doi: 10.1073/pnas.1814323115. Epub 2018 Oct 24.
8
Pancan-meQTL: a database to systematically evaluate the effects of genetic variants on methylation in human cancer.泛癌甲基化 QTL(pan-cancer methylation quantitative trait loci,panCan-meQTL)数据库:用于系统评估遗传变异对人类癌症中甲基化影响的数据库。
Nucleic Acids Res. 2019 Jan 8;47(D1):D1066-D1072. doi: 10.1093/nar/gky814.
9
Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic disease.囊性纤维化中 DNA 甲基化的动态变化与肺部疾病:单基因疾病带来的启示。
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