Evidence map›Paper›PMID 33839219›Full record

ArticleMolecular and cellular endocrinology2021

The endocannabinoid system and retinoic acid signaling combine to influence bone growth.

Daniel Fraher, Robert J Mann, Matthew J Dubuisson, Megan K Ellis, Tingsheng Yu, Ken Walder, Alister C Ward, Christoph Winkler, Yann Gibert

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Role of vitamins in the development and treatment of osteoporosis (Review).International journal of molecular medicine · 2025
    Review
  7. Article
  8. 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

9 authors at 3 institutions in 3 countries.

Daniel FraherMetabolic Genetic Diseases Laboratory, Metabolic Research Unit, Deakin University School of Medicine, Geelong, VIC, 3216, Australia.
Robert J MannMetabolic Genetic Diseases Laboratory, Metabolic Research Unit, Deakin University School of Medicine, Geelong, VIC, 3216, Australia.
Matthew J DubuissonUniversity of Mississippi Medical Center, Dept of Cell and Molecular Biology, 2500 North State Street, Jackson, MS, 39216, USA.
Megan K EllisMetabolic Genetic Diseases Laboratory, Metabolic Research Unit, Deakin University School of Medicine, Geelong, VIC, 3216, Australia.
Tingsheng YuDepartment of Biological Sciences and Centre for Bioimaging Sciences, National University of Singapore, Singapore.
Ken WalderMetabolic Genetic Diseases Laboratory, Metabolic Research Unit, Deakin University School of Medicine, Geelong, VIC, 3216, Australia.
Alister C WardMetabolic Genetic Diseases Laboratory, Metabolic Research Unit, Deakin University School of Medicine, Geelong, VIC, 3216, Australia.
Christoph WinklerDepartment of Biological Sciences and Centre for Bioimaging Sciences, National University of Singapore, Singapore.
Yann GibertMetabolic Genetic Diseases Laboratory, Metabolic Research Unit, Deakin University School of Medicine, Geelong, VIC, 3216, Australia; University of Mississippi Medical Center, Dept of Cell and Molecular Biology, 2500 North State Street, Jackson, MS, 39216, USA. Electronic address: ygibert@umc.edu.
Deakin University · AUNational University of Singapore · SGState Street (United States) · US

Funding

The role of leptin in autoimmune-associated hypertensionP20GM104357 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI TAYLOR, ERIN BASSFORD · 2013 to 2022
$23.4M
NIGMS NIH HHS P20 GM104357
6 · The paper itself

Abstract

Osteoporosis is an increasing burden on public health as the world-wide population ages and effective therapeutics are severely needed. Two pathways with high potential for osteoporosis treatment are the retinoic acid (RA) and endocannabinoid system (ECS) signaling pathways. We sought to elucidate the roles that these pathways play in bone development and maturation. Here, we use chemical treatments to modulate the RA and ECS pathways at distinct early, intermediate, and late times bone development in zebrafish. We further assessed osteoclast activity later in zebrafish and medaka. Finally, by combining sub-optimal doses of AR and ECS modulators, we show that enhancing RA signaling or reducing the ECS promote bone formation and decrease osteoclast abundance and activity. These data demonstrate that RA signaling and the ECS can be combined as sub-optimal doses to influence bone growth and may be key targets for potential therapeutics.

Indexed as

AnimalsBone DevelopmentEmbryo, NonmammalianEndocannabinoidsGene Expression Regulation, DevelopmentalOryziasOsteoclastsOsteogenesisOsteonectinRimonabantSignal TransductionSp7 Transcription FactorTranscription FactorsTretinoinZebrafishZebrafish ProteinsEndocannabinoidsOsteonectinRimonabantRunx2a protein, zebrafishRunx2b protein, zebrafishsp7 protein, zebrafishSp7 Transcription FactorTranscription FactorsTretinoinZebrafish ProteinsEndocannabinoidMedakaOsteoblastOsteoclastRetinoic acidZebrafish

Identifiers

PMID33839219
PMCPMC8127411
OpenAlexW3155332396

What OpenQuestion holds

Textmetadata
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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.