Genetics and Epigenetics of Nasal Polyposis: A Systematic Review

被引:11
作者
Martin, M. J. [1 ,2 ,3 ]
Garcia-Sanchez, A. [1 ,2 ,4 ]
Estravis, M. [1 ,2 ,4 ]
Gil-Melcon, M. [5 ]
Isidoro-Garcia, M. [1 ,2 ,6 ,7 ]
Sanz, C. [1 ,2 ,8 ]
Davila, I [1 ,2 ,4 ,9 ]
机构
[1] Inst Biomed Res Salamanca, IBSAL, Salamanca, Spain
[2] Network Cooperat Res Hlth RET ARADyAL, Salamanca, Spain
[3] Univ Salamanca, Dept Biochem & Mol Biol, Salamanca, Spain
[4] Univ Salamanca, Dept Biomed & Diagnost Sci, Salamanca, Spain
[5] Hosp Univ Salamanca, Dept Otorhinolaryngol, Serv Otorrinolaringol, Salamanca, Spain
[6] Hosp Univ Salamanca, Dept Clin Biochem, Serv Bioquim Clin, Salamanca, Spain
[7] Univ Salamanca, Dept Med, Salamanca, Spain
[8] Univ Salamanca, Dept Microbiol & Genet, Salamanca, Spain
[9] Hosp Univ Salamanca, Dept Immunoallergy, Serv Inmunoalergia, Salamanca, Spain
关键词
Nasal polyposis; Gene variants; Polymorphisms; Epigenetics; Chronic rhinosinusitis; Systematic review; EOSINOPHILIC CHRONIC RHINOSINUSITIS; SINGLE-NUCLEOTIDE POLYMORPHISMS; GENOME-WIDE ASSOCIATION; CYSTIC-FIBROSIS; MATRIX METALLOPROTEINASE-2; PROMOTER POLYMORPHISM; CHRONIC SINUSITIS; POTENTIAL ROLE; EXPRESSION; RISK;
D O I
10.18176/jiaci.0673
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Chronic rhinosinusitis (CRS) is an inflammatory disease of the nose and paranasal sinuses that is often associated with nasal polyposis (CRSwNP) in the most severe cases. As in other complex diseases, genetic factors are thought to play an important role in the risk and development of the disease. Environment may also modulate the epigenetic signature in affected patients. In the present systematic review, we aimed to compile all published data on genetic and epigenetic variations in CRSwNP since 2000. We found 104 articles, 24 of which were related to epigenetic studies. We identified more than 150 genetic variants in 99 genes involved in the pathogenesis of nasal polyposis. These were clustered into 8 main networks, linking genes involved in inflammation and immune response (eg, MHC), cytokine genes (eg, TNF), leukotriene metabolism, and the extracellular matrix. A total of 89 miRNAs were also identified; these are associated mainly with biological functions such as the cell cycle, inflammation, and the immune response. We propose a potential relationship between genes and the miRNAs identified that may open new lines of investigation. An in-depth knowledge of gene variants and epigenetic traits could help us to design more tailored treatment for patients with CRSwNP.
引用
收藏
页码:196 / 211
页数:16
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