Abstract

BackgroundOsteoarthritis (OA) is the most common form of arthritis and a leading cause of disability. This study attempted to investigate the key mRNAs and miRNAs related to OA.Patients and methodsFrom April 17th, 2018 to May 17th, 2018, five patients with OA and three normal controls were enrolled in this present study. To identify the differentially expressed mRNAs (DEmRNAs) and miRNAs (DEmiRNAs) between patients with OA and normal controls, RNA-sequencing was performed. Then, DEmiRNA-target DEmRNAs analysis and functional annotation of DEmiRNA-target DEmRNAs were performed. To validate the RNA-sequencing results, quantitative real time-PCR (RT-PCR) and western blot analysis were performed as well.ResultsA total of 1068 DEmRNAs, 21 DEmiRNAs and 395 DEmiRNA-DEmRNA pairs were identified in synovial tissues of patients with OA. The functional annotation of DEmiRNA-target DEmRNAs revealed that Pathways in cancer and PI3K-Akt signaling pathway were significantly enriched Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. QRT-PCR and western blot results revealed that except for TLR7, the expression level of the others was consistent with the RNA-sequencing results, generally.ConclusionThe findings of this present study may provide new clues for the roles of DEmRNAs and DEmiRNAs in the pathogenesis of OA.

Highlights

  • Osteoarthritis (OA) is the most frequent musculoskeletal disease and leads to functional decline and loss in quality of life [1]

  • A total of 1068 Differentially expressed mRNA (DEmRNA), 21 differentially expressed miRNAs (DEmiRNA) and 395 DEmiRNA-DEmRNA pairs were identified in synovial tissues of patients with OA

  • The functional annotation of DEmiRNA-target DEmRNAs revealed that Pathways in cancer and PI3K-Akt signaling pathway were significantly enriched Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways

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Summary

Introduction

Osteoarthritis (OA) is the most frequent musculoskeletal disease and leads to functional decline and loss in quality of life [1]. There is no effective treatment to prevent the initiation and progression of the disease while the severity of OA often worsens with age [2]. It estimates that among population over 60 years old, there was 9.6% of men and 18% of women suffer from symptomatic OA in the worldwide [3]. Little was known of the function of miRNAs at the stage when it is first identified in the early 1990’s by Lee. Osteoarthritis (OA) is the most common form of arthritis and a leading cause of disability. This study attempted to investigate the key mRNAs and miRNAs related to OA

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