| Literature DB >> 32030826 |
Su Ni1, Chao Xu2, Chao Zhuang3, Gongyin Zhao3, Chenkai Li1, Yuji Wang1, Xihu Qin4.
Abstract
It is known that miR-34a can promote the apoptosis of chondrocytes, which directly contribute to osteoarthritis (OA). Through bioinformatics analysis, we found that long noncoding RNA LUADT1 may interact with miR-34a. We, therefore, further investigate the interactions between them in osteoarthritis. We found that LUADT1 was downregulated, while miR-34a was upregulated in OA synovial fluid. Correlation analysis revealed no significant correlation between them. Overexpression experiment also revealed no significant effects of LUADT1 and miR-34a on the expression of each other. However, the dual-luciferase assay showed that LUADT1 and miR-34a can directly interact with each other. Moreover, LUADT1 overexpression led to the upregulation of SIRT1, which is a downstream target of miR-34a. Cell apoptosis showed that LUADT1 and SIRT1 overexpression led to decreased, while miR-34a led to increased apoptotic rates of chondrocytes. Therefore, LUADT1 regulates miR-34a/SIRT1 to participate in chondrocyte apoptosis.Entities:
Keywords: LUADT1; SIRT1; chondrocytes; miR-34a; osteoarthritis
Year: 2020 PMID: 32030826 DOI: 10.1002/jcb.29637
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429