Evidence map›Paper›PMID 37842749›Full record

ReviewAmerican journal of physiology. Cell physiology2023

MicroRNA-138: an emerging regulator of skeletal development, homeostasis, and disease.

Victor Gustavo Balera Brito, Austin Bell-Hensley, Audrey McAlinden

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. The role of microRNAs in calcific aortic valve disease.Frontiers in cardiovascular medicine · 2025
    Review
  7. The Role of miR-138 in Cardiovascular Diseases.BioMed research international · 2025
    Review
  8. Autologous hGMSC-Derived iPS: A New Proposal for Tissue Regeneration.International journal of molecular sciences · 2024
    Article
  9. 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

3 authors at 1 institution in 1 country.

Victor Gustavo Balera BritoDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, United States.ORCID 0000-0001-5508-3825
Austin Bell-HensleyDepartment of Biomedical Engineering, Washington University School of Medicine, St. Louis, Missouri, United States.ORCID 0000-0003-1498-3012
Audrey McAlindenDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, United States.ORCID 0000-0001-8433-4224
Washington University in St. Louis · US

Funding

MicroRNA regulation of bone formation and repairR01AR075730 · NIAMS · WASHINGTON UNIVERSITY · PI MCALINDEN, AUDREY · 2020 to 2024
$2.4M
Modulation of MicroRNAs to Engineer a Layered Osteochondral Tissue ConstructF31AR082294 · NIAMS · WASHINGTON UNIVERSITY · PI BELL-HENSLEY, AUSTIN PATRICK · 2023 to 2023
$45k
NIAMS NIH HHS F31 AR082294NIAMS NIH HHS R01 AR075730
6 · The paper itself

Abstract

Noncoding microRNAs are powerful epigenetic regulators of cellular processes by their ability to target and suppress expression of numerous protein-coding mRNAs. This multitargeting function is a unique and complex feature of microRNAs. It is now well-described that microRNAs play important roles in regulating the development and homeostasis of many cell/tissue types, including those that make up the skeletal system. In this review, we focus on microRNA-138 (miR-138) and its effects on regulating bone and cartilage cell differentiation and function. In addition to its reported role as a tumor suppressor, miR-138 appears to function as an inhibitor of osteoblast differentiation. This review provides additional information on studies that have attempted to alter miR-138 expression in vivo as a means to dampen ectopic calcification or alter bone mass. However, a review of the published literature on miR-138 in cartilage reveals a number of contradictory and inconclusive findings with respect to regulating chondrogenesis and chondrocyte catabolism. This highlights the need for more research in understanding the role of miR-138 in cartilage biology and disease. Interestingly, a number of studies in other systems have reported miR-138-mediated effects in dampening inflammation and pain responses. Future studies will reveal if a multifunctional role of miR-138 involving suppression of ectopic bone, inflammation, and pain will be beneficial in skeletal conditions such as osteoarthritis and heterotopic ossification.

Indexed as

MicroRNAsCartilageCell DifferentiationChondrocytesHomeostasisHumansInflammationPainMicroRNAsMIRN138 microRNA, humanbonecartilagemicroRNAmiR-138osteogenesis

Identifiers

PMID37842749
PMCPMC10861148
OpenAlexW4387661805

What Socratic 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 Socratic graph.