Epigenetic Regulations in the Pathogenesis of Periodontitis

被引:22
作者
Luo, Yu [1 ,2 ]
Peng, Xian [1 ]
Duan, Dingyu [1 ,3 ]
Liu, Chengcheng [1 ,3 ]
Xu, Xin [1 ,2 ]
Zhou, Xuedong [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, 14,Sect 3,Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Dept Operat Dent & Endodont, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp Stomatol, Dept Periodont, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Periodontitis; epigenetics; DNA methylation; histone modification; microRNA; epigenetic regulation; TUMOR-NECROSIS-FACTOR; HISTONE DEACETYLASE INHIBITORS; GENE PROMOTER METHYLATION; GINGIVAL EPITHELIAL-CELLS; MESENCHYMAL STEM-CELLS; SINGLE-NUCLEOTIDE POLYMORPHISMS; PORPHYROMONAS-GINGIVALIS; AGGRESSIVE PERIODONTITIS; FACTOR-ALPHA; CYTOKINE PROFILES;
D O I
10.2174/1574888X12666170718161740
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: Periodontitis is a multifactorial infectious disease that affects a large population worldwide. Oral microorganisms and susceptible host have been proposed to be the prerequisite for the development of periodontitis. Recently, the involvement of epigenetic modifications in the development of periodontitis has been suggested. Objectives: This review aims to detail recent discoveries involving the epigenetic alterations in periodontitis, and discuss the possible epigenetic mechanisms contributing to the expression of periodontitis-related genes. Conclusions: The expression of inflammatory cytokines during periodontitis is regulated at epigenetic level by mechanisms such as DNA methylation, histone modification and miRNAs. In addition, periodontal pathogens and their virulence factors could induce epigenetic alterations of periodontal tissues, and thus affect the progression and prognosis of periodontitis. The involvement of epigenetic modifications during periodontitis not only advances our knowledge on the pathogenesis of periodontitis, but may also lead to the identification of potential therapeutic targets of this oral disease.
引用
收藏
页码:144 / 150
页数:7
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