CiliOPD: a ciliopathy-associated COPD endotype

被引:13
|
作者
Perotin, Jeanne-Marie [1 ,2 ]
Polette, Myriam [1 ,3 ]
Deslee, Gaetan [1 ,2 ]
Dormoy, Valerian [1 ]
机构
[1] Univ Reims, INSERM, CHU Maison Blanche, P3Cell UMRS 1250,SFR CAP SANTE, 45 Rue Cognacq Jay, F-51092 Reims, France
[2] Hop Maison Blanche, CHU Reims, Dept Resp Dis, F-51092 Reims, France
[3] Hop Maison Blanche, CHU Reims, Dept Biopathol, F-51092 Reims, France
关键词
COPD; Cilia; Transcriptomic; IDENTIFY;
D O I
10.1186/s12931-021-01665-4
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The pathophysiology of chronic obstructive pulmonary disease (COPD) relies on airway remodelling and inflammation. Alterations of mucociliary clearance are a major hallmark of COPD caused by structural and functional cilia abnormalities. Using transcriptomic databases of whole lung tissues and isolated small airway epithelial cells (SAEC), we comparatively analysed cilia-associated and ciliopathy-associated gene signatures from a set of 495 genes in 7 datasets including 538 non-COPD and 508 COPD patients. This bio-informatics approach unveils yet undescribed cilia and ciliopathy genes associated with COPD including NEK6 and PROM2 that may contribute to the pathology, and suggests a COPD endotype exhibiting ciliopathy features (CiliOPD).
引用
收藏
页数:7
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