Evidence map›Paper›PMID 39910695›Full record

ArticleJournal of cellular and molecular medicine2025

Progranulin Protects Against Osteoporosis by Regulating Osteoclast and Osteoblast Balance via TNFR Pathway.

Shaoyi Wang, Hengyan Zhang, Yanbin Zhu, Xiaocong Zhou, Haoxin Zhai, Qiting He, Xuetao Zhu, Yuanqiang Zhang

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 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. Article
  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

8 authors.

Shaoyi WangDepartment of Orthopaedic Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, P. R. China.
Hengyan ZhangThe Second Children & Women's Healthcare of Jinan City, Jinan, Shandong, P. R. China.
Yanbin ZhuDepartment of Orthopaedic Surgery, The Third Hospital of Hebei Medical University, Shijiazhuang, P. R. China.
Xiaocong ZhouHealth Management Center, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong, P. R. China.
Haoxin ZhaiDepartment of Orthopaedic Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, P. R. China.
Qiting HeDepartment of Orthopaedic Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, P. R. China.
Xuetao ZhuDepartment of Orthopaedic Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, P. R. China.
Yuanqiang ZhangDepartment of Orthopaedic Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, P. R. China.ORCID 0009-0009-9561-2889

Funding

National Natural Science Foundation youth project of China 82402758
6 · The paper itself

Abstract

Osteoporosis is a disease of bone metabolism caused by an imbalance between osteoclast-mediated bone destruction and osteoblast-mediated bone formation. Tumour necrosis factor α (TNFα) has been reported to promote osteoclast generation and inhibit osteoblast generation. Progranulin (PGRN), which has a strong anti-inflammatory effect, interacts with tumour necrosis factor receptor (TNFR). Serum and bone tissues from patients with or without osteoporosis were collected to analyse the relationship between PGRN content and bone metabolic markers. The role of TNFα and PGRN in osteoclast differentiation was explored by using RAW 264.7 cells and BMMs. MC3T3-E1 cells and BMSCs were used to observe the role of TNFα and PGRN in osteoblast differentiation. The PGRN content in the serum and bone tissues of osteoporosis patients was lower than that in the serum and bone tissues of nonosteoporosis patients. TNFα promoted osteoclast differentiation, while PGRN inhibited this effect by interacting with TNFR1. PGRN inhibited TNFα-mediated attenuation of osteoblast differentiation by interacting with TNFR1. Moreover, PGRN alone promoted osteoblast differentiation by interacting with TNFR2. Our findings reveal that PGRN can effectively inhibit TNFα-induced osteoporosis and has a certain osteogenic effect. This discovery might provide a potential target for osteoporosis treatment.

Indexed as

OsteoblastsOsteoclastsOsteoporosisProgranulinsReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Type ISignal TransductionAgedAnimalsCell DifferentiationFemaleHumansMaleMiceMiddle AgedOsteogenesisGRN protein, humanProgranulinsReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IITumor Necrosis Factor-alphaosteoporosisProgranulinTNFR pathway

Identifiers

PMID39910695
PMCPMC11798871

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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.