These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Inhibition of miR-203 Ameliorates Osteoarthritis Cartilage Degradation in the Postmenopausal Rat Model: Involvement of Estrogen Receptor α.
    Author: Tian L, Su Z, Ma X, Wang F, Guo Y.
    Journal: Hum Gene Ther Clin Dev; 2019 Dec; 30(4):160-168. PubMed ID: 31711313.
    Abstract:
    miR-203 is known to target estrogen receptor α (ERα) in various cancer cell lines, such as MCF-7. However, whether miR-203 regulates ERα and contributes to the onset and progression of osteoarthritis (OA) is poorly understood. A combined protocol of the bilateral ovariectomy and the intra-articular monosodium iodoacetate injection was applied to establish a postmenopausal OA model in rats. Real-time quantitative polymerase chain reaction was used to detect miR-203 and mRNAs and Western blotting was exploited to quantify the expression levels on the protein level. Enzyme-linked immunosorbent assays were deployed to detect the expression of matrix metalloproteinase-1 (MMP-1), MMP-3, prostaglandin E2 (PGE2), and collagen type II degradation (CTX-II) in serum samples. Dual-luciferase reporter assay was utilized to confirm the direct binding of miR-203 on ERα in postmenopausal OA rats. Expression of miR-203 was elevated; while ERα mRNA and protein were downregulated in postmenopausal OA rats, compared with sham rats. Dual-luciferase reporter assay confirmed miR-203 bound and negatively regulated ERα, resulting in promoted cellular inflammation and cartilage destruction in postmenopausal OA rats. Suppression of miR-203 using a specific inhibitor ameliorated cartilage degradation in postmenopausal OA rats. miR-203 is pivotal in the onset and progression of OA in the postmenopausal rat model, and holds promise for a therapeutic target of OA treatment.
    [Abstract] [Full Text] [Related] [New Search]