Evidence map›Paper›PMID 37057210›Full record

ReviewInternational journal of medical sciences2023

MiR-30 Family: A Novel Avenue for Treating Bone and Joint Diseases?

Jinming Huang, Yi Li, Siyi Zhu, Liqiong Wang, Lin Yang, Chengqi He

Open access · goldAbstract readReview
In one paragraph

Review in International journal of medical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.8field-weighted citation impact, top 5% of its field
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

19 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. let-7c-5p promotes fracture healing by downregulating CDK8.Journal of orthopaedic surgery and research · 2026
    Article
  6. Article
  7. Article
  8. Programmed cell death in triple-negative breast cancer.Cellular & molecular biology letters · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. International journal of molecular sciences · 2024
    Article
  17. Article
  18. Article
  19. Observational
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

6 authors at 2 institutions in 1 country.

Jinming HuangDepartment of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China. Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Yi LiDepartment of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China. Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Siyi ZhuDepartment of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China. Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Liqiong WangDepartment of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China. Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Lin YangDepartment of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China. Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Chengqi HeDepartment of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China. Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Sichuan University · CNWest China Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone and joint diseases are a group of clinically heterogeneous diseases characterized by various bone strength disorders, bone structural defects and bone mass abnormalities. Common bone diseases include osteoporosis, skeletal dysplasia, and osteosarcoma, and common joint diseases include osteoarthritis, rheumatoid arthritis, and degenerative disc disease. all of them lead to high medical costs. The miR-30 family consists of a total of 5 members: miR-30a, miR-30b, miR-30c, miR-30d and miR-30e. Accumulating evidence has indicated that the miR-30 family may be involved in the occurrence and development of bone and joint diseases. For example, miR-30a is highly expressed in blood samples of osteoporosis patients, miR-30a/b increases in cartilage tissue of osteoarthritis patients, and lower expression of miR-30c is associated with higher malignance and shorter survival time of osteosarcoma. Mechanistically, by targeting crucial transcription factors (RUNX2, SOX9, beclin-1, etc.), the miR-30 family regulates some critical pathways of bone homeostasis (Wnt/β-Catenin, mTOR, PI3K/AKT, etc.). In view of the distinct actions of the miR-30 family on bone metabolism, we hypothesize that the miR-30 family may be a new remedy for the clinical treatment and prevention of some bone and joint diseases.

Indexed as

Bone NeoplasmsMicroRNAsOsteoarthritisOsteoporosisOsteosarcomaHumansPhosphatidylinositol 3-KinasesMicroRNAsPhosphatidylinositol 3-Kinasesbone tumorextracellular vesiclesmetabolic bone diseasesmiR-30osteoarthritisosteoporosisvascular calcification

Identifiers

PMID37057210
PMCPMC10087628
OpenAlexW4320502761

What OpenQuestion 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 OpenQuestion graph.