Evidence map›Paper›PMID 39764467›Full record

ReviewFrontiers in pharmacology2024

Exosomal communication: a pivotal regulator of bone homeostasis and a potential therapeutic target.

Qian-Yun Ye, Yan Cui, Hao-Yu Wang, Ling-Yu Li, Jian-Bing Chen, Xiao-Feng Zhu, Zhi-Jian Xue, Rong-Hua Zhang

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Bone organoid construction and evolution.Journal of orthopaedic translation · 2025
    Review
  4. Article
  5. Review
  6. 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.

Qian-Yun Ye *Department of Traditional Chinese Medicine, First Affiliated Hospital of Jinan University, Guangzhou, China.
Yan Cui *College of Traditional Chinese Medicine, Jinan University, Guangzhou, China.
Hao-Yu Wang *College of Traditional Chinese Medicine, Jinan University, Guangzhou, China.
Ling-Yu LiCollege of Pharmacy, Jinan University, Guangzhou, China.
Jian-Bing ChenCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, China.
Xiao-Feng ZhuCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, China.
Zhi-Jian XueDepartment of Traditional Chinese Medicine, First Affiliated Hospital of Jinan University, Guangzhou, China.
Rong-Hua ZhangCollege of Pharmacy, Jinan University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone homeostasis encompasses two interrelated aspects: bone remodeling and cartilage metabolism. Disruption of bone homeostasis can lead to the development of metabolic bone diseases such as osteoporosis and osteoarthritis. The maintenance of bone homeostasis is a complex process that does not solely rely on the functions of the bone tissue itself. In fact, bone tissue is not an isolated entity; it is closely connected to other tissues in the body via exosomes. Within this interconnectivity, exosomes derived from both bone and non-bone cells interfere with each other, forming a complex regulatory network. Therefore, with cell origin as the guiding principle, we have delineated the bone regulatory network of exosomes, elaborated on the specific roles and regulatory mechanisms of exosomes derived from common cell types (cells within the skeletal microenvironment, stem cells from extra-osseous tissues, vascular-derived cells, muscle-derived cells, and neurogenic cells) in bone formation, bone resorption, and cartilage metabolism. We have also discussed the challenges faced in the field of exosome research related to bone homeostasis, unveiled the critical role of exosomes in maintaining bone homeostasis, and proposed that exosomes could serve as highly valuable therapeutic targets for metabolic bone diseases.

Indexed as

bone homeostasisexosomeextracellular vesicleosteoarthritisosteoporosis

Identifiers

PMID39764467
PMCPMC11700997

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.