Novel insights into the interaction between N6-methyladenosine methylation and noncoding RNAs in musculoskeletal

Juanjuan Han1,2, Hui Kong1, Xueqiang Wang2,3

  • 1College of Kinesiology, Shenyang Sport University, Shenyang, China.

Cell Proliferation
|June 23, 2022
PubMed
Abstract

Insights

N6-methyladenosine (m6A) RNA modification and noncoding RNAs (ncRNAs) interact to regulate musculoskeletal disorders (MSDs). Targeting these interactions offers a promising therapeutic strategy for MSDs like osteoarthritis and osteoporosis.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Musculoskeletal disorders (MSDs) are inflammatory and degenerative diseases with poorly understood molecular mechanisms.
  • Noncoding RNA (ncRNA) N6-methyladenosine (m6A) modification is crucial in the pathophysiology of MSDs.
  • Understanding the interplay between m6A and ncRNAs offers new therapeutic avenues for MSDs.

Purpose of the Study:

  • To review the interaction between m6A RNA methylation and ncRNAs in the molecular regulatory mechanisms of MSDs.
  • To provide insights into the pathophysiological mechanisms of MSDs.
  • To explore ncRNA m6A targeted therapy for MSDs.

Main Methods:

  • A comprehensive literature search was conducted using keywords related to MSDs and RNA modifications.
  • Relevant articles were systematically reviewed and summarized.
  • Key findings on the mutual regulation between m6A and ncRNAs in MSDs were synthesized.

Main Results:

  • Intervertebral disc degeneration (IDD), osteoporosis (OP), osteosarcoma (OS), and osteoarthritis (OA) are common MSDs affecting muscle, bone, and cartilage.
  • The precise pathogenesis of MSDs remains unclear, with no effective treatments currently available.
  • Mutual regulation between m6A and ncRNAs (microRNAs, long ncRNAs, circular RNAs) is evident in MSDs, impacting skeletal homeostasis.

Conclusions:

  • m6A and ncRNAs interact to regulate biological processes implicated in IDD, OP, OS, and OA.
  • This interaction provides novel insights into MSD pathophysiology.
  • Targeting m6A-modified ncRNAs presents a promising therapeutic strategy for MSDs.

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