Role of microRNA in the pathogenesis of systemic sclerosis tissue fibrosis and vasculopathy

被引:63
作者
Henry, Tyler W. [1 ,2 ,3 ]
Mendoza, Fabian A. [1 ,2 ,4 ]
Jimenez, Sergio A. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Jefferson Inst Mol Med, Suite 509A-Bluemle Life Sci,Bldg 233 S 10th St, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Scleroderma Ctr, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Philadelphia, PA 19107 USA
[4] Thomas Jefferson Univ, Dept Med, Div Rheumatol, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
microRNA; Systemic sclerosis; Tissue fibrosis; Vasculopathy; Endothelial-mesenchymal transition; ENDOTHELIAL-MESENCHYMAL TRANSITION; GROWTH-FACTOR-BETA; DOWN-REGULATION; COLLAGEN EXPRESSION; DERMAL FIBROBLASTS; SIGNALING PATHWAY; GENE-EXPRESSION; I COLLAGEN; PLASMINOGEN-ACTIVATOR; SCLERODERMA FIBROSIS;
D O I
10.1016/j.autrev.2019.102396
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic Sclerosis (SSc) pathogenesis involves multiple immunological, vascular and fibroproliferative abnormalities that contribute to a severe and complex clinical picture. Vasculopathy and fibroproliferative alterations are two hallmark pathological processes in SSc that are responsible for the most severe clinical manifestations of the disease and determine its clinical outcome and mortality. However, the pathogenesis of SSc vasculopathy and of the uncontrolled SSc fibrotic process remain incompletely understood. Recent investigations into the molecular pathways involved in these processes have identified an important role for epigenetic processes that contribute to overall disease progression and have emphasized microRNAs (miRNAs) as crucial epigenetic regulators. MiRNAs hold unique potential for elucidating SSc pathogenesis, improving diagnosis and developing effective targeted therapies for the disease. This review examines the important role that miRNAs play in the development and regulation of vascular and fibroproliferative alterations associated with SSc pathogenesis and their possible participation in the establishment of pathogenetic connections between these two processes. This review also emphasizes that further understanding of the involvement of miRNA in SSc fibrosis and vasculopathy will very likely provide novel future research directions and allow for the identification of groundbreaking therapeutic interventions within these processes. MiR-21, miR-31, and miR-155 are of particular interest owing to their important involvement in both SSc vasculopathy and fibroproliferative alterations.
引用
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页数:10
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