Evidence map›Paper›PMID 42559155›Full record

ReviewFrontiers in endocrinology2026

Regulation of osteoclastogenesis and bone resorption by fatty acid metabolism: mechanisms and therapeutic opportunities.

Yingying Jin, Chanchan Zheng, Yuyan Xiang, Zichen Zheng, Jianquan Chen

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Yingying Jin *Department of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China.
Chanchan Zheng *Department of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China.
Yuyan Xiang *Department of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China.
Zichen ZhengDepartment of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China.
Jianquan ChenDepartment of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone remodeling is orchestrated by osteoclast-mediated resorption and osteoblast-mediated formation. Dysregulated hyperactivity of osteoclasts is a central driver of pathological bone loss in multiple osteolytic diseases, such as postmenopausal osteoporosis, rheumatoid arthritis, and peri-implant osteolysis. Although the core RANKL signaling cascade that governs osteoclast differentiation has been well characterized, accumulating evidence indicates that RANKL also triggers profound metabolic reprogramming during osteoclastogenesis, among which fatty acid (FA) metabolism has emerged as a critical regulator of osteoclast fate and function. In this review, we provide a comprehensive analysis of how FA metabolic pathways regulate osteoclast differentiation, fusion, and function. We first briefly introduce the core FA metabolic pathways relevant to osteoclasts, including FA uptake, FA oxidation, FA storage,

Indexed as

Bone ResorptionFatty AcidsOsteoclastsOsteogenesisAnimalsCell DifferentiationHumansFatty Acidsbone resorptionde novo lipogenesisfatty acid metabolismfatty acid β-oxidationosteoclastogenesisosteolytic diseasestherapeutic targeting

Identifiers

PMID42559155
PMCPMC13439972

What Socratic holds

Textmetadata
LicenceCC BY
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.