Evidence map›Paper›PMID 40151080›Full record

ReviewCurrent molecular medicine2026

Bone Marrow Mesenchymal Stem Cell Senescence in the Development of Osteoporosis: Mechanisms, Interventions, and Future Directions.

Chengen Li, Bo Li, Jiuchao Zhang, Kun Liu, Gang Du, Cunliang Guo, Zhenguo Yang

Abstract readReview
In one paragraph

Review in Current molecular medicine, 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. Pharmaceutical biology · 2026
    Article
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

7 authors.

Chengen LiDepartment of Orthopedia, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, 250000, China.
Bo LiDepartment of Orthopedia, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, 250000, China.
Jiuchao ZhangDepartment of Orthopedia, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, 250000, China.
Kun LiuDepartment of Orthopedia, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, 250000, China.
Gang DuDepartment of Orthopedia, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, 250000, China.
Cunliang GuoDepartment of Integrative Chinese and Western Medicine, Tianjin University of Traditional Chinese Medicine, Jinghai District, Tianjin, 301617, China.
Zhenguo YangDepartment of Orthopedia, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, 250000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis, a significant age-related disease, is marked by diminished bone density and an elevated risk of fractures, representing a considerable global health challenge. Bone marrow mesenchymal stem cells (BMSCs) are essential in maintaining bone integrity through their differentiation into osteoblasts, which are crucial for bone formation. Nevertheless, the aging of BMSCs diminishes their regenerative abilities and intensifies inflammation, thereby playing a critical role in osteoporosis pathogenesis. This review explores the intricate mechanisms of BMSC senescence and its influence on osteoporosis, detailing cellular and molecular markers, such as oxidative stress, the senescence-associated secretory phenotype (SASP), and pivotal signaling pathways, including P53, PI3K/mTOR, and autophagy. We assess current interventions aimed at reducing BMSC senescence, with an emphasis on pharmacological methods like melatonin and antioxidants, alongside nonpharmacological strategies, such as exercise and dietary supplementation with omega-3 fatty acids. Furthermore, the challenges and limitations of translating these strategies into clinical applications are addressed, highlighting the necessity for personalized medicine to accommodate treatment outcome variability. Future research directions should focus on emerging therapeutic targets and novel interventions, such as gene editing technologies and advanced tissue engineering techniques. By integrating these strategies, this review endeavors to enhance the understanding and treatment of osteoporosis, emphasizing the critical need to target BMSC senescence to develop effective therapies.

Indexed as

Bone Marrow CellsCellular SenescenceMesenchymal Stem CellsOsteoporosisAnimalsHumansOxidative StressSignal TransductionBone marrow mesenchymal stem cellscell senescencecellularmolecular markersomega-3 fatty acidsosteoporosisSASP

Identifiers

PMID40151080
PMCPMC13678605

What OpenQuestion holds

Textmetadata
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.