Nrf2 signaling pathway: focus on oxidative stress in osteoporosis
Abstract
The nuclear factor erythrocyte 2-related factor-2 (Nrf2) signaling pathway is an important regulatory factor for bone homeostasis in osteoporosis. It is also regarded as a key pathway of antioxidant stress and is closely related to the pathological process of osteoporosis. Osteoporosis is a chronic metabolic bone disease characterized by an imbalance between osteoclast bone resorption and osteoblast bone formation, and oxidative stress is the core driving factor that induces bone metabolic imbalance. Studies have confirmed that the Nrf2 signaling pathway plays a key role in the pathological process of osteoporosis and in maintaining the homeostasis of the bone microenvironment. Here, we review the current knowledge about the role of the Nrf2 signaling pathway in osteoporosis and analyze its interaction with bone metabolism-related signaling pathways such as Wnt/β-catenin and NF-κB. By systematically integrating the existing research evidence, the therapeutic value of targeted activation of Nrf2 in improving bone metabolic imbalance, inhibiting osteoclastic activity and promoting bone formation is reviewed. Multiple studies have shown that the Nrf2 pathway, as a core antioxidant mechanism, effectively inhibits the excessive activation of osteoclasts and hyperresorption by antagonizing oxidative stress in osteoporosis, and dynamically regulates bone homeostasis. It forms a cross-regulatory network with key signaling pathways such as Wnt/β-catenin (promoting bone formation) and NF-κB (promoting inflammation), jointly influencing the level of oxidative stress and the balance of bone remodeling. Importantly, targeted activation of Nrf2 demonstrates significant therapeutic potential, capable of simultaneously promoting bone formation, inhibiting osteoclastic activity, and restoring the dynamic balance of bone metabolism, thereby providing multi-dimensional intervention in the pathological process of osteoporosis. The Nrf2 signaling pathway plays a core protective role in the pathogenesis of osteoporosis by regulating oxidative stress and related pathological links in multiple dimensions. Its interaction with key bone metabolic pathways provides a theoretical basis for the development of therapeutic strategies targeting Nrf2 and is expected to become a novel therapeutic target for improving bone metabolic imbalance.
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Nrf2 may alleviate the suppression of osteogenic differentiation by inflammatory factors through inhibition of NF-κB activation.
“Mechanistically, Nrf2 may alleviate the suppression of osteogenic differentiation by inflammatory factors through the inhibition of NF-κB activation38, while concurrently promoting the expression of osteogenic genes by regulating the Wnt/β-catenin signaling pathway54.”
From Intelligence-responsive wettability switch coating on magnesium implants for treating osteoporotic fracture (2026) · cites this paper as [38]
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Qi, G., Ma, T., Wang, Y., Chen, K., Yan, Y., Li, Z., Deng, N., Tseng, C., Li, B., Zheng, Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-72683-3 · Cited by 2 · see citing works
“As a key transcription factor, Nrf2 is essential in the cellular defense against oxidative stress, enhancing osteogenic differentiation and suppressing osteoclast activity 38 .”
- Authors
- Gu, H.-Y., Liu, N., Lin, F.-X., & Yin, J.
- Affiliations
- Ganzhou People's Hospital (CN)
- Corresponding author
- Gu, Hou-yun
- Yin, Jun
- Venue
- Osteoporosis International
- Published
- 2025-07-15
- Volume
- 36
- Issue
- 10
- Pages
- 1837-1854
- ISSN
- 0937-941X (ISSN-L)
- 1433-2965
- OpenAlex
- W4412457304
- Cited by
- 10
- References
- 237
- Citations by year
- 2026: 10
- FWCI
- 0.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Osteoporosis International (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- Nrf2 signaling, osteoporosis, oxidative stress, bone homeostasis, bone remodeling, osteoclast activity, bone resorption, bone formation, Wnt/β-catenin signaling, NF-κB signaling, antioxidant defense, therapeutic target
- MeSH terms
- Animals, Humans, Osteoporosis, Signal Transduction, Bone Remodeling, Oxidative Stress, NF-E2-Related Factor 2, Wnt Signaling Pathway
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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