Evidence mapPaperPMID 41006700Full record

ArticleCommunications biology2025

Zingerone treats postmenopausal osteoporosis via increased ferroptosis sensitivity by p53-mediated regulation of SAT1 and GPX4 expression.

Hao Li, Fangming Cao, Dian Liu, Lin Tao

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

4 authors.

Hao Li *Department of Orthopedics, First Hospital of China Medical University, Shenyang, Liaoning, PR China.
Fangming Cao *Department of Orthopedics, First Hospital of China Medical University, Shenyang, Liaoning, PR China.
Dian LiuDepartment of Orthopedics, First Hospital of China Medical University, Shenyang, Liaoning, PR China.
Lin TaoDepartment of Orthopedics, First Hospital of China Medical University, Shenyang, Liaoning, PR China. taolindr@163.com.ORCID http://orcid.org/0000-0002-1702-9833

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22-321-32-08
6 · The paper itself

Abstract

Zingerone, a component of dried ginger, has known anti-ulcer and bone growth-promoting effects, but its impact on postmenopausal osteoporosis (PO) is unclear. This study investigates the therapeutic potential and underlying mechanisms of zingerone in PO. A concentration-dependent effect identified on osteoclast precursors: at low concentrations, zingerone maintains low ROS levels, enhance proliferation, and facilitates bone remodelling; at high concentrations, it elevates ROS levels, enhances ferroptosis sensitivity, and suppresses osteoclast formation. Zingerone significantly improves bone mass in an ovariectomised mouse model of PO. Metabolomics identifies 869 differential metabolites linked to glutathione and purine metabolism. Transcriptomics highlights pathways including ferroptosis, leukocyte migration, and cell adhesion. In RAW264.7 cells, zingerone modulates p53, enhances ferroptosis sensitivity, increasing ROS and Fe

Indexed as

FerroptosisGuaiacolOsteoporosis, PostmenopausalPhospholipid Hydroperoxide Glutathione PeroxidaseTumor Suppressor Protein p53AnimalsFemaleHumansMiceMice, Inbred C57BLReactive Oxygen Speciesglutathione peroxidase 4, mouseGuaiacolPhospholipid Hydroperoxide Glutathione PeroxidaseReactive Oxygen SpeciesTrp53 protein, mouseTumor Suppressor Protein p53zingerone

Identifiers

PMID41006700
PMCPMC12474940

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.