Evidence map›Paper›PMID 42614599›Full record

ReviewPhenomics (Cham, Switzerland)2026

Autophagy: A Novel Therapeutic Target for Osteoporosis.

Li Meng, Zhongkai Zhang, Yufeng Huang, Chengzu Zheng, Lingling Wang, Zhuoran Li, Ying Wang, Yanxia Li, Mingjie Liu, Baobing Zhao and 1 more

Abstract readReview
In one paragraph

Review in Phenomics (Cham, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Li MengDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.ORCID 0000-0001-9510-7756
Zhongkai ZhangDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Yufeng HuangDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Chengzu ZhengDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Lingling WangDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Zhuoran LiDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Ying WangDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Yanxia LiDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Mingjie LiuDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.
Baobing ZhaoDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.ORCID 0000-0001-8522-4764
Yuan LiDepartment of Pharmacology, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012 Shandong China.ORCID 0000-0002-4552-5180

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is an evolutionarily conserved catabolic process in eukaryotes, which plays a vital role in the maintenance of cellular homeostasis. The occurrence of autophagy depends on lysosome, which is responsible for eliminating the dysfunctional cellular components, including misfolded proteins, impaired organelles and pathogens. Osteoporosis (OP) is a common bone metabolic disease, and it needs more therapeutic strategies that could restore the imbalance between bone formation and bone resorption, which is the main pathophysiological feature of OP. Interstingly, increasing evidence shows that autophagy is closely involved in bone metabolism, and its aberrant level leads to various skeletal system disorders, including OP. Autophagy regulates the survival, differentiation and function of bone marrow mesenchymal stromal cells (BMSCs), osteoblasts, osteocytes and osteoclasts, which are the major cell types in the bone microenvironment. Herein, we summarized the important advances of autophagy in bone metabolism, and the promising therapeutic strategies for OP by targeting autophagy. This review is aimed at providing novel insights for the prevention and treatment of OP via regulation of autophagy.

Indexed as

AutophagyBone developmentBone marrow mesenchymal stromal cellsBone metabolismOsteoporosis

Identifiers

PMID42614599
PMCPMC13481957

What OpenQuestion holds

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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.