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Review
. 2021 Sep 16:12:755230.
doi: 10.3389/fphar.2021.755230. eCollection 2021.

Update on Novel Non-Operative Treatment for Osteoarthritis: Current Status and Future Trends

Affiliations
Review

Update on Novel Non-Operative Treatment for Osteoarthritis: Current Status and Future Trends

Tao Chen et al. Front Pharmacol. .

Abstract

Osteoarthritis (OA) is a leading cause of pain and disability which results in a reduced quality of life. Due to the avascular nature of cartilage, damaged cartilage has a finite capacity for healing or regeneration. To date, conservative management, including physical measures and pharmacological therapy are still the principal choices offered for OA patients. Joint arthroplasties or total replacement surgeries are served as the ultimate therapeutic option to rehabilitate the joint function of patients who withstand severe OA. However, these approaches are mainly to relieve the symptoms of OA, instead of decelerating or reversing the progress of cartilage damage. Disease-modifying osteoarthritis drugs (DMOADs) aiming to modify key structures within the OA joints are in development. Tissue engineering is a promising strategy for repairing cartilage, in which cells, genes, and biomaterials are encompassed. Here, we review the current status of preclinical investigations and clinical translations of tissue engineering in the non-operative treatment of OA. Furthermore, this review provides our perspective on the challenges and future directions of tissue engineering in cartilage regeneration.

Keywords: cartilage regeneration; gene; non-operative; osteoarthritis; scaffold; tissue engineering.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Risk factors and pathogenic process of OA. Squares on the left side include the risk factors responsible for the development of OA, and the circle on the right side represents the pathogenic process of OA. ADAMTS = a disintegrin and metalloproteinase with thrombospondin motifs; MMP = matrix metalloproteinase; ECM = extracellular matrix; IL = interleukin; TNF = tumor necrosis factor; IFN = Interferon; BMP = bone morphogenic protein; TGF = transforming growth factor; VEGF = Vascular endothelial growth factor.
FIGURE 2
FIGURE 2
Future trends of tissue engineering in treating OA. Proper cell selection, appropriate bioactive stimulus, and perfect design of scaffolds are central to tissue engineering. Novel scientific technologies, including CRISPR gene editing, 3D bioprinting, and AI should be used to facilitate the development of tissue engineering in treating OA.

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