Evidence map›Paper›PMID 37019926›Full record

ArticleScientific reports2023

Impaired retinoic acid signaling in cerebral cavernous malformations.

Nastasja Grdseloff, Gwenola Boulday, Claudia J Rödel, Cécile Otten, Daphné Raphaelle Vannier, Cécile Cardoso, Eva Faurobert, Deepika Dogra, Elisabeth Tournier-Lasserve, Salim Abdelilah-Seyfried

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Plasma water TMetabolic brain disease · 2024
    Observational
  2. 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

10 authors at 7 institutions in 4 countries.

Nastasja Grdseloff *Institute of Biochemistry and Biology, Department of Zoophysiology, University of Potsdam, Karl-Liebknecht-Strasse 24-25, 14476, Potsdam, Germany.
Gwenola Boulday *InsermNeuroDiderot, Université Paris Cité, 75019, Paris, France.
Claudia J RödelInstitute of Biochemistry and Biology, Department of Zoophysiology, University of Potsdam, Karl-Liebknecht-Strasse 24-25, 14476, Potsdam, Germany.
Cécile OttenInstitute of Biochemistry and Biology, Department of Zoophysiology, University of Potsdam, Karl-Liebknecht-Strasse 24-25, 14476, Potsdam, Germany.
Daphné Raphaelle VannierInstitute for Advanced Biosciences, INSERM 1209 CNRS, University Grenoble Alpes, 5309, Grenoble, France.
Cécile CardosoInsermNeuroDiderot, Université Paris Cité, 75019, Paris, France.
Eva FaurobertInstitute for Advanced Biosciences, INSERM 1209 CNRS, University Grenoble Alpes, 5309, Grenoble, France.
Deepika DograInstitute of Biochemistry and Biology, Department of Zoophysiology, University of Potsdam, Karl-Liebknecht-Strasse 24-25, 14476, Potsdam, Germany.
Elisabeth Tournier-LasserveInsermNeuroDiderot, Université Paris Cité, 75019, Paris, France.
Salim Abdelilah-SeyfriedInstitute of Biochemistry and Biology, Department of Zoophysiology, University of Potsdam, Karl-Liebknecht-Strasse 24-25, 14476, Potsdam, Germany. salim.seyfried@uni-potsdam.de.
University of Potsdam · DEAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRInserm · FRNeuroDiderot · FRUniversité Grenoble Alpes · FRUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The capillary-venous pathology cerebral cavernous malformation (CCM) is caused by loss of CCM1/Krev interaction trapped protein 1 (KRIT1), CCM2/MGC4607, or CCM3/PDCD10 in some endothelial cells. Mutations of CCM genes within the brain vasculature can lead to recurrent cerebral hemorrhages. Pharmacological treatment options are urgently needed when lesions are located in deeply-seated and in-operable regions of the central nervous system. Previous pharmacological suppression screens in disease models of CCM led to the discovery that treatment with retinoic acid improved CCM phenotypes. This finding raised a need to investigate the involvement of retinoic acid in CCM and test whether it has a curative effect in preclinical mouse models. Here, we show that components of the retinoic acid synthesis and degradation pathway are transcriptionally misregulated across disease models of CCM. We complemented this analysis by pharmacologically modifying retinoic acid levels in zebrafish and human endothelial cell models of CCM, and in acute and chronic mouse models of CCM. Our pharmacological intervention studies in CCM2-depleted human umbilical vein endothelial cells (HUVECs) and krit1 mutant zebrafish showed positive effects when retinoic acid levels were increased. However, therapeutic approaches to prevent the development of vascular lesions in adult chronic murine models of CCM were drug regiment-sensitive, possibly due to adverse developmental effects of this hormone. A treatment with high doses of retinoic acid even worsened CCM lesions in an adult chronic murine model of CCM. This study provides evidence that retinoic acid signaling is impaired in the CCM pathophysiology and suggests that modification of retinoic acid levels can alleviate CCM phenotypes.

Indexed as

Hemangioma, Cavernous, Central Nervous SystemAdultAnimalsBrainHumansHuman Umbilical Vein Endothelial CellsMiceMicrotubule-Associated ProteinsProto-Oncogene ProteinsZebrafishMicrotubule-Associated ProteinsProto-Oncogene Proteins

Identifiers

PMID37019926
PMCPMC10076292
OpenAlexW4362608498

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.