Evidence map›Paper›PMID 39595628›Full record

ReviewBiomolecules2024

Targeting the mTOR-Autophagy Axis: Unveiling Therapeutic Potentials in Osteoporosis.

Rongjin Chen, Chenhui Yang, Fei Yang, Ao Yang, Hefang Xiao, Bo Peng, Changshun Chen, Bin Geng, Yayi Xia

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Targeting CEBPA/ALOX15B attenuates postmenopausal osteoporosis by inhibiting ferroptosis through the AMPK/mTOR signaling pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
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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

9 authors.

Rongjin ChenDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Chenhui YangDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Fei YangDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Ao YangDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Hefang XiaoDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Bo PengDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Changshun ChenDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Bin GengDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Yayi XiaDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou 730030, China.

Funding

Lanzhou Science and Technology Plan Program 2021-RC-102National Natural Science Foundation of China 81960403National Natural Science Foundation of China 82060405National Natural Science Foundation of China 82360436
6 · The paper itself

Abstract

Osteoporosis (OP) is a widespread age-related disorder marked by decreased bone density and increased fracture risk, presenting a significant public health challenge. Central to the development and progression of OP is the dysregulation of the mechanistic target of the rapamycin (mTOR)-signaling pathway, which plays a critical role in cellular processes including autophagy, growth, and proliferation. The mTOR-autophagy axis is emerging as a promising therapeutic target due to its regulatory capacity in bone metabolism and homeostasis. This review aims to (1) elucidate the role of mTOR signaling in bone metabolism and its dysregulation in OP, (2) explore the interplay between mTOR and autophagy in the context of bone cell activity, and (3) assess the therapeutic potential of targeting the mTOR pathway with modulators as innovative strategies for OP treatment. By examining the interactions among autophagy, mTOR, and OP, including insights from various types of OP and the impact on different bone cells, this review underscores the complexity of mTOR's role in bone health. Despite advances, significant gaps remain in understanding the detailed mechanisms of mTOR's effects on autophagy and bone cell function, highlighting the need for comprehensive clinical trials to establish the efficacy and safety of mTOR inhibitors in OP management. Future research directions include clarifying mTOR's molecular interactions with bone metabolism and investigating the combined benefits of mTOR modulation with other therapeutic approaches. Addressing these challenges is crucial for developing more effective treatments and improving outcomes for individuals with OP, thereby unveiling the therapeutic potentials of targeting the mTOR-autophagy axis in this prevalent disease.

Indexed as

AutophagyOsteoporosisSignal TransductionTOR Serine-Threonine KinasesAnimalsBone and BonesHumansMTOR protein, humanTOR Serine-Threonine Kinasesautophagybone metabolismmTOR signaling pathwayosteoporosistherapeutic targeting

Identifiers

PMID39595628
PMCPMC11591800

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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.