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Updated: Aug 31, 2025

Software-Assisted Quantitative Measurement of Osteoarthritic Subchondral Bone Thickness
Published on: March 18, 2022
RNA binding proteins in osteoarthritis
Qian Yi1,2,3, Zhenhan Deng4, Jiaji Yue1
1Department of Bone and Joint Surgery, Shenzhen Second People's Hospital (The First Affiliated Hospital of Shenzhen University), Shenzhen, China.
Abstract:
Osteoarthritis (OA) is a common chronic degenerative joint disease worldwide. The pathological features of OA are the erosion of articular cartilage, subchondral bone sclerosis, synovitis, and metabolic disorder. Its progression is characterized by aberrant expression of genes involved in inflammation, proliferation, and metabolism of chondrocytes. Effective therapeutic strategies are limited, as mechanisms underlying OA pathophysiology remain unclear. Significant research efforts are ongoing to elucidate the complex molecular mechanisms underlying OA focused on gene transcription. However, posttranscriptional alterations also play significant function in inflammation and metabolic changes related diseases. RNA binding proteins (RBPs) have been recognized as important regulators in posttranscriptional regulation. RBPs regulate RNA subcellular localization, stability, and translational efficiency by binding to their target mRNAs, thereby controlling their protein expression. However, their role in OA is less clear. Identifying RBPs in OA is of great importance to better understand OA pathophysiology and to figure out potential targets for OA treatment. Hence, in this manuscript, we summarize the recent knowledge on the role of dysregulated RBPs in OA and hope it will provide new insight for OA study and targeted treatment.
Insights
RNA binding proteins (RBPs) are crucial for regulating gene expression after transcription. Understanding their role in osteoarthritis (OA) is key to developing new treatments for this common joint disease.
Area of Science:
- Biochemistry
- Molecular Biology
- Rheumatology
Background:
- Osteoarthritis (OA) is a prevalent degenerative joint disease characterized by cartilage erosion, subchondral bone changes, and inflammation.
- Current therapeutic strategies for OA are limited due to incomplete understanding of its complex molecular mechanisms.
- While gene transcription is heavily studied, posttranscriptional regulation by RNA binding proteins (RBPs) also significantly impacts OA-related inflammation and metabolism.
Purpose of the Study:
- To review the current knowledge on the function of dysregulated RNA binding proteins (RBPs) in osteoarthritis (OA).
- To highlight the importance of identifying RBPs involved in OA pathophysiology.
- To explore RBPs as potential therapeutic targets for osteoarthritis treatment.
Main Methods:
- Literature review of recent studies on RNA binding proteins (RBPs) and osteoarthritis (OA).
- Analysis of the role of RBPs in posttranscriptional gene regulation relevant to OA.
- Synthesis of information on the impact of RBPs on chondrocyte function and inflammation in OA.
Main Results:
- RBPs are critical regulators of RNA stability, localization, and translation, influencing protein expression.
- Dysregulation of specific RBPs is implicated in the inflammatory and metabolic changes observed in OA.
- The precise role of most RBPs in OA pathogenesis remains to be fully elucidated.
Conclusions:
- Identifying and understanding the function of RBPs in OA is essential for advancing OA research.
- RBPs represent promising targets for the development of novel therapeutic strategies for osteoarthritis.
- Further investigation into RBP-mediated posttranscriptional regulation offers new insights into OA pathophysiology.
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