Evidence map›Paper›PMID 40034405›Full record

ReviewDrug design, development and therapy2025

The Roles of Forkhead Box O3a (FOXO3a) in Bone and Cartilage Diseases - A Narrative Review.

Zhenyu Wu, Wang Zhan, Longhuo Wu, Luhu Yu, Xunlu Xie, Fang Yu, Weihao Kong, Shengrong Bi, Shiwei Liu, Guoqiang Yin and 1 more

Abstract readReview
In one paragraph

Review in Drug design, development and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Mechanisms of Protection Against Oxidative Stress During Hibernation.International journal of molecular sciences · 2026
    Review
  6. Research progress on the mechanism of FOXO protein in sepsis.Apoptosis : an international journal on programmed cell death · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Forkhead box O proteins in chondrocyte aging and diseases.Journal of orthopaedic translation · 2025
    Review
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Zhenyu WuDepartment of Medical Imaging, First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, People's Republic of China.
Wang ZhanFirst Clinical Medical College, Gannan Medical University, Ganzhou, 341000, People's Republic of China.
Longhuo WuCollege of Pharmacy, Gannan Medical University, Ganzhou, 341000, People's Republic of China.ORCID 0000-0002-3899-9599
Luhu YuDepartment of Clinical Laboratory, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.
Xunlu XieDepartment of Pathology, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.
Fang YuDepartment of Joint Surgery, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.
Weihao KongDepartment of Joint Surgery, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.
Shengrong BiDepartment of Joint Surgery, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.
Shiwei LiuDepartment of Joint Surgery, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.
Guoqiang YinDepartment of Joint Surgery, Ganzhou Hospital Affiliated to Nanchang University, Ganzhou, 341000, People's Republic of China.
Jianguo ZhouDepartment of Joint Surgery, Ganzhou People's Hospital, Ganzhou, 341000, People's Republic of China.ORCID 0000-0002-3824-2916

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone and cartilage diseases are significantly associated with musculoskeletal disability. However, no effective drugs are available to cure them. FOXO3a, a member of the FOXO family, has been implicated in cell proliferation, ROS detoxification, autophagy, and apoptosis. The biological functions of FOXO3a can be modulated by post-translational modifications (PTMs), such as phosphorylation and acetylation. Several signaling pathways, such as MAPK, NF-κB, PI3K/AKT, and AMPK/Sirt1 pathways, have been implicated in the development of bone and cartilage diseases by mediating the expression of FOXO3a. In particular, FOXO3a acts as a transcriptional factor in mediating the expression of various genes, such as MnSOD, CAT, BIM, BBC3, and CDK6. FOXO3a plays a critical role in the metabolism of bone and cartilage. In this article, we mainly discussed the biological functions of FOXO3a in bone and cartilage diseases, such as osteoporosis (OP), osteoarthritis (OA), rheumatoid arthritis (RA), ankylosing spondylitis (AS), and intervertebral disc degeneration (IDD). FOXO3a can promote osteogenic differentiation, induce osteoblast proliferation, inhibit osteoclast activity, suppress chondrocyte apoptosis, and reduce inflammatory responses. Collectively, up-regulation of FOXO3a expression shows beneficial effects, and FOXO3a has become a potential target for bone and cartilage diseases.

Indexed as

Bone DiseasesCartilage DiseasesForkhead Box Protein O3AnimalsHumansForkhead Box Protein O3FOXO3 protein, humanankylosing spondylitisFOXO3aintervertebral disc degenerationosteoarthritisosteoporosisrheumatoid arthritis

Identifiers

PMID40034405
PMCPMC11874768

What Socratic holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.