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자료유형
학술저널
저자정보
Jiang Hua (The First Affiliated Hospital of Guangxi Medical University) Moro Abu (The First Affiliated Hospital of Guangxi Medical University) Wang Jiaqi (The First Affiliated Hospital of Guangxi Medical University) Meng Dihua (The First Affiliated Hospital of Guangxi Medical University) Zhan Xinli (The First Affiliated Hospital of Guangxi Medical University) Wei Qingjun (The First Affiliated Hospital of Guangxi Medical University)
저널정보
대한생화학·분자생물학회 Experimental and Molecular Medicine Experimental and Molecular Medicine 제53권
발행연도
2021.9
수록면
1 - 10 (10page)
DOI
10.1038/s12276-021-00662-3

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Recent studies have demonstrated the pivotal role played by microRNAs (miRNAs) in the etiopathogenesis of intervertebral disc degeneration (IDD). The study of miRNA intervention in IDD models may promote the advancement of miRNA-based therapeutic strategies. The aim of the current study was to investigate whether intradiscal delivery of miRNA can attenuate IDD development. Our results showed that miR-338-3p expression was significantly increased in the nucleus pulposus (NP) of patients with IDD. Moreover, there was a statistically significant positive correlation between the expression level of miR-338-3p and the severity of IDD. Our functional studies showed that miR-338-3p significantly influenced the expression of extracellular matrix synthesis genes, as well as the proliferation and apoptosis of NP cells. Mechanistically, miR-338-3p aggravated IDD progression by directly targeting SIRT6, a negative regulator of the MAPK/ERK pathway. Intradiscal injection of antagomir-338-3p significantly decelerated IDD development in mouse models. Our study is the first to identify miR-338-3p as a mediator of IDD and thus may be a promising target for rescuing IDD.

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