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RESEARCH PAPER / 2024-09-17

NRF2 in age-related musculoskeletal diseases: Role and treatment prospects.

Xiangyu Zhang, Hengzhen Li, Lin Chen, Yuxiang Wu, Yusheng Li

Department of Orthopedics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.Department of Orthopedics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China. · pubmed

Abstract

The NRF2 pathway is a metabolic- and redox-sensitive signaling axis in which the transcription factor controls the expression of a multitude of genes that enable cells to survive environmental stressors, such as oxidative stress, mainly by inducing the expression of cytoprotective genes. Basal NRF2 levels are maintained under normal physiological conditions, but when exposed to oxidative stress, cells activate the NRF2 pathway, which is crucial for supporting cell survival. Recently, the NRF2 pathway has been found to have novel functions in metabolic regulation and interplay with other signaling pathways, offering novel insights into the treatment of various diseases. Numerous studies have shown that targeting its pathway can effectively investigate the development and progression of age-related musculoskeletal diseases, such as sarcopenia, osteoporosis, osteoarthritis, and intervertebral disc degeneration. Appropriate regulation of the NRF2 pathway flux holds promise as a means to improve musculoskeletal function, thereby providing a new avenue for drug treatment of age-related musculoskeletal diseases in clinical settings. The review summarized an overview of the relationship between NRF2 and cellular processes such as oxidative stress, apoptosis, inflammation, mitochondrial dysfunction, ferroptosis, and autophagy, and explores the potential of targeted NRF2 regulation in the treatment of age-related musculoskeletal diseases.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper discusses the NRF2 pathway's role in age-related musculoskeletal diseases, which is relevant to longevity research as it explores potential therapeutic targets that could address underlying mechanisms of aging. However, the focus remains on treating symptoms of specific diseases rather than directly addressing the root causes of aging itself. The findings contribute to the understanding of NRF2 in the context of age-related conditions, but the impact is limited as it does not present groundbreaking insights or transformative approaches to longevity.

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