The complex landscape of microRNAs in articular cartilage: biology, pathology, and therapeutic targets

被引:84
作者
Endisha, Helal [1 ,2 ,3 ,4 ]
Rockel, Jason [1 ,2 ]
Jurisica, Igor [1 ,2 ,5 ,6 ,7 ]
Kapoor, Mohit [1 ,2 ,3 ,4 ]
机构
[1] Univ Hlth Network, Toronto Western Hosp, Arthrit Program, Toronto, ON, Canada
[2] Univ Hlth Network, Krembil Res Inst, Div Genet & Dev, Toronto, ON, Canada
[3] Univ Toronto, Dept Surg, 60 Leonard Ave, Toronto, ON M5T 2S8, Canada
[4] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[5] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[6] Univ Toronto, Dept Comp Sci, Toronto, ON, Canada
[7] Slovak Acad Sci, Inst Neuroimmunol, Bratislava, Slovakia
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
MESENCHYMAL STEM-CELLS; ARTHRITIS SYNOVIAL FIBROBLASTS; INDUCED INFLAMMATORY INJURY; AGE-RELATED-CHANGES; CHONDROCYTE APOPTOSIS; KNEE OSTEOARTHRITIS; STROMAL CELLS; TGF-BETA; NEUROVASCULAR PLASTICITY; INTRAARTICULAR INJECTION;
D O I
10.1172/jci.insight.121630
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The disabling degenerative disease osteoarthritis (OA) is prevalent among the global population. Articular cartilage degeneration is a central feature of OA; therefore, a better understanding of the mechanisms that maintain cartilage homeostasis is vital for developing effective therapeutic interventions. MicroRNAs (miRs) modulate cell signaling pathways and various processes in articular cartilage via posttranscriptional repression of target genes. As dysregulated miRs frequently alter the homeostasis of articular cartilage, modulating select miRs presents a potential therapeutic opportunity for OA. Here, we review key miRs that have been shown to modulate cartilage-protective or -destructive mechanisms and signaling pathways. Additionally, we use an integrative computational biology approach to provide insight into predicted miR gene targets that may contribute to OA pathogenesis, and highlight the complexity of miR signaling in OA by generating both unique and overlapping gene targets of miRs that mediate protective or destructive effects. Early OA detection would enable effective prevention; thus, miRs are being explored as diagnostic biomarkers. We discuss these ongoing efforts and the applicability of miR mimics and antisense inhibitors as potential OA therapeutics.
引用
收藏
页数:15
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