Evidence map›Paper›PMID 40866352›Full record

ArticleCell death & disease2025

Targeting Irgm1 to combat osteoporosis: suppressing ROS and restoring bone remodeling.

Zichen Cui, Guanghui Gu, Fei Chen, Jianyi Li, Xiaofan Du, Shuqing Chen, Han Zhang, Chenxu Li, Jiale Shao, Jiayi Xi and 3 more

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
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  10. 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

13 authors.

Zichen CuiDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Guanghui GuDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Fei ChenDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Jianyi LiDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Xiaofan DuDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Shuqing ChenDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Han ZhangDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Chenxu LiDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Jiale ShaoDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China.
Jiayi XiUniversity of Illinois at Urbana-Champaign, Champaign, IL, USA.
Yukun DuDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China. qdfydyk0728@163.com.
Qinghua ZhaoDepartment of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. qinghua.zhao@shgh.cn.
Yongming XiDepartment of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, China. xym700118@qdu.edu.cn.ORCID http://orcid.org/0000-0002-2921-0699

Funding

Taishan Scholar Project of Shandong Province tstp20250511
6 · The paper itself

Abstract

The accumulation of reactive oxygen species (ROS) leads to enhanced osteoclast activity, causing severe bone destruction in postmenopausal osteoporosis. Immunity-related GTPase family M member 1 (Irgm1) plays an essential role in affecting the production of intracellular ROS. To detect whether deletion of Irgm1 could suppress osteoclastogenesis through cellular redox regulation, we first evaluated whether the Irgm1 level was significantly elevated in mice bone marrow-derived monocytes/macrophages (BMDMs) from ovariectomy (OVX)-induced osteoporosis mice. Moreover, bioinformatics network analysis was performed to identify Irgm1 as a key upregulated gene during osteoclast differentiation. Next, we found that macrophage-specific Irgm1 knockout (Irgm1-cKO, Lyz2-Cre; Irgm1

Indexed as

Bone RemodelingGTP-Binding ProteinsOsteoporosisReactive Oxygen SpeciesAnimalsBone ResorptionCell DifferentiationFemaleHumansKelch-Like ECH-Associated Protein 1MacrophagesMiceMice, Inbred C57BLMice, KnockoutNF-E2-Related Factor 2OsteoclastsGTP-Binding ProteinsIfi1 protein, mouseKeap1 protein, mouseKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2Reactive Oxygen Species

Identifiers

PMID40866352
PMCPMC12391319

What OpenQuestion holds

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Registered trials

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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.