Evidence map›Paper›PMID 27754752›Full record

ArticleSmall GTPases2018

RhoA controls retinoid signaling by ROCK dependent regulation of retinol metabolism.

Alberto García-Mariscal, Karine Peyrollier, Astrid Basse, Esben Pedersen, Ralph Rühl, Jolanda van Hengel, Cord Brakebusch

Open access · bronzeAbstract read
In one paragraph

Article in Small GTPases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Role of cellular retinol-binding protein, type 1 and retinoid homeostasis in the adult mouse heart: A multi-omic approach.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Retinoic acid signaling promotes the cytoskeletal rearrangement of embryonic epicardial cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    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

7 authors at 3 institutions in 3 countries.

Alberto García-Mariscala Department of Biomedical Sciences , BRIC, University of Copenhagen , Copenhagen , Denmark.
Karine Peyrolliera Department of Biomedical Sciences , BRIC, University of Copenhagen , Copenhagen , Denmark.
Astrid Bassea Department of Biomedical Sciences , BRIC, University of Copenhagen , Copenhagen , Denmark.
Esben Pedersena Department of Biomedical Sciences , BRIC, University of Copenhagen , Copenhagen , Denmark.
Ralph Rühlb Laboratory of Nutritional Bioactivation and Bioanalysis, Research Center of Molecular Medicine, University of Debrecen , Hungary.
Jolanda van Hengelc Department of Basic Medical Sciences , Faculty of Medicine and Health Sciences, Ghent University , Ghent , Belgium.ORCID 0000-0003-0645-0435
Cord Brakebuscha Department of Biomedical Sciences , BRIC, University of Copenhagen , Copenhagen , Denmark.
University of Copenhagen · DKGhent University · BEUniversity of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ubiquitously expressed small GTPase RhoA is essential for embryonic development and mutated in different cancers. Functionally, it is well described as a regulator of the actin cytoskeleton, but its role in gene regulation is less understood. Using primary mouse keratinocytes with a deletion of the RhoA gene, we have now been exploring how the loss of RhoA affects gene expression. Performing transcription factor reporter assays, we found a significantly decreased activity of a RAR luciferase reporter in RhoA-null keratinocytes. Inhibition of the RhoA effector ROCK in control cells reproduced this phenotype. ATRA and retinal, but not retinol increased RAR reporter activity of keratinocytes with impaired RhoA/ROCK signaling, suggesting that retinol metabolism is regulated by RhoA/ROCK signaling. Furthermore a significant percentage of known ATRA target genes displayed altered expression in RhoA-null keratinocytes. These data reveal an unexpected link between the cytoskeletal regulator RhoA and retinoid signaling and uncover a novel pathway by which RhoA regulates gene expression.

Indexed as

Signal TransductionAnimalsCell SizeGene Expression RegulationKeratinocytesLigandsMiceRetinoidsrhoA GTP-Binding Proteinrho-Associated KinasesSkinStem CellsVitamin ALigandsRetinoidsrhoA GTP-Binding Proteinrho-Associated KinasesVitamin Aretinoic acidRhoAROCKskinstem cells

Identifiers

PMID27754752
PMCPMC5997168
OpenAlexW2537332047

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.