Evidence map›Paper›PMID 40360512›Full record

ArticleNature communications2025

FABP4 inhibition suppresses bone resorption and protects against postmenopausal osteoporosis in ovariectomized mice.

Qian Xie, Xiangfu Du, Jianhui Liang, Yanni Shen, Yufan Ling, Zhengji Huang, Zekai Ke, Tai Li, Bing Song, Tailin Wu and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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  3. Strategies for Targeting Mitochondria in the Treatment of Breast Cancer.ACS pharmacology & translational science · 2026
    Review
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  20. 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

12 authors.

Qian Xie *Center for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. xqqx1996@163.com.ORCID http://orcid.org/0000-0002-3755-8599
Xiangfu Du *Center for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Jianhui LiangCenter for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Yanni ShenCenter for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.ORCID http://orcid.org/0000-0003-4924-1705
Yufan LingCenter for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Zhengji HuangDepartment of orthopedics, Shenzhen University General Hospital, Shenzhen, China.
Zekai KeDepartment of orthopedics, Shenzhen University General Hospital, Shenzhen, China.
Tai LiCenter for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Bing SongCenter for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Tailin WuDepartment of Orthopaedics and Traumatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China. tl_spine@163.com.ORCID http://orcid.org/0000-0002-3209-4422
Yan WangCenter for Translational Medicine Research and Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. yan.wang@siat.ac.cn.ORCID http://orcid.org/0000-0003-0671-7312
Huiren TaoDepartment of Orthopaedics and Traumatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China. huiren_tao@163.com.ORCID http://orcid.org/0000-0002-6373-2968

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82174033National Natural Science Foundation of China (National Science Foundation of China) T2350710233
6 · The paper itself

Abstract

Postmenopausal osteoporosis (PMOP) is a condition in women caused by estrogen deficiency, characterized by reduced bone mass and increased fracture risk. Fatty acid-binding protein 4 (FABP4), a lipid-binding protein involved in metabolism and inflammation, has emerged as a key regulator in metabolic disorders and bone resorption; however, its direct role in PMOP remains unclear. Here, we show that serum FABP4 levels in PMOP patients negatively correlate with bone mineral density, a trend also observed in ovariectomized mice. FABP4 promotes osteoclast formation and bone resorption without affecting osteoblast differentiation. The FABP4 inhibitor BMS309403 suppresses osteoclast differentiation by modulating calcium signaling and inhibiting the Ca

Indexed as

Bone ResorptionFatty Acid-Binding ProteinsOsteoporosis, PostmenopausalAlendronateAnimalsBiphenyl CompoundsBone DensityCell DifferentiationFemaleHumansMiceMice, Inbred C57BLMiddle AgedOsteoblastsOsteoclastsOsteogenesis2-(2'-(5-ethyl-3,4-diphenyl-1H-pyrazol-1-yl)biphenyl-3-yloxy)acetic acidAlendronateBiphenyl CompoundsFABP4 protein, humanFabp4 protein, mouseFatty Acid-Binding ProteinsPyrazoles

Identifiers

PMID40360512
PMCPMC12075751

What OpenQuestion 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 OpenQuestion graph.