Evidence map›Paper›PMID 36700983›Full record

ArticleBasic research in cardiology2023

The endothelial-enriched lncRNA LINC00607 mediates angiogenic function.

Frederike Boos, James A Oo, Timothy Warwick, Stefan Günther, Judit Izquierdo Ponce, Melina Lopez, Diba Rafii, Giulia Buchmann, Minh Duc Pham, Zahraa S Msheik and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Basic research in cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
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  5. LINC00607 facilitates endothelial VEGF-A receptor FLT1 splicing.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  6. Article
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  11. Role of eRNAs in Cardiovascular Diseases.Current cardiology reviews · 2026
    Review
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  18. Article
  19. Automated High-Throughput Live Cell Monitoring of Scratch Wound Closure.Biomedical engineering and computational biology · 2024
    Article
  20. 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

28 authors at 6 institutions in 4 countries.

Frederike BoosInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.ORCID http://orcid.org/0000-0002-1842-5459
James A OoInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Timothy WarwickInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Stefan GüntherMax-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.
Judit Izquierdo PonceInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Melina LopezInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Diba RafiiInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Giulia BuchmannInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Minh Duc PhamGenome Biologics, Frankfurt, Germany.
Zahraa S MsheikMax-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.
Tianfu LiInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Sandra SeredinskiInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Shaza HaydarInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Sepide KashefiolaslDepartment of Neurosurgery, University Hospital Frankfurt, Frankfurt, Germany.
Karl H PlateInstitute of Neurology (Edinger Institute), Neuroscience Center, Goethe University, Frankfurt, Germany.
Rüdiger BehrDZHK (German Center for Cardiovascular Research), Partner Site Göttingen, Göttingen, Germany.
Matthias MietschDZHK (German Center for Cardiovascular Research), Partner Site Göttingen, Göttingen, Germany.
Jaya KrishnanGerman Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Soni S PullamsettiMax-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.
Sofia-Iris BibliGerman Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Rabea HinkelDZHK (German Center for Cardiovascular Research), Partner Site Göttingen, Göttingen, Germany.
Andrew H BakerCentre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, Scotland.ORCID http://orcid.org/0000-0003-1441-5576
Reinier A BoonGerman Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Marcel H SchulzGerman Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Ilka WittigInstitut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.
Francis J MillerDepartment of Medicine, Vanderbilt University Medical Center, Nashville, USA.
Ralf P Brandes *Institut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany. Brandes@vrc.uni-frankfurt.de.
Matthias S Leisegang *Institut für Kardiovaskuläre Physiologie, Fachbereich Medizin der Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany. Leisegang@vrc.uni-frankfurt.de.ORCID http://orcid.org/0000-0002-6084-6484
Goethe University Frankfurt · DEMax Planck Institute for Heart and Lung Research · DEGerman Primate Center · DEMaastricht University · NLUniversity of Veterinary Medicine Hannover, Foundation · DEVeterans Health Administration · US

Funding

Regulation of the Nox1 NADPH Oxidase in Vascular Smooth Muscle CellsI01BX001729 · VA · IOWA CITY VA MEDICAL CENTER · PI MILLER, FRANCIS J · 2012 to 2020
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BLRD VA I01 BX001729British Heart Foundation CH/11/2/28733British Heart Foundation PG/20/10347British Heart Foundation ReGenLncBritish Heart Foundation RG/20/5/34796British Heart Foundation SP/F/22/150029
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) can act as regulatory RNAs which, by altering the expression of target genes, impact on the cellular phenotype and cardiovascular disease development. Endothelial lncRNAs and their vascular functions are largely undefined. Deep RNA-Seq and FANTOM5 CAGE analysis revealed the lncRNA LINC00607 to be highly enriched in human endothelial cells. LINC00607 was induced in response to hypoxia, arteriosclerosis regression in non-human primates, post-atherosclerotic cultured endothelial cells from patients and also in response to propranolol used to induce regression of human arteriovenous malformations. siRNA knockdown or CRISPR/Cas9 knockout of LINC00607 attenuated VEGF-A-induced angiogenic sprouting. LINC00607 knockout in endothelial cells also integrated less into newly formed vascular networks in an in vivo assay in SCID mice. Overexpression of LINC00607 in CRISPR knockout cells restored normal endothelial function. RNA- and ATAC-Seq after LINC00607 knockout revealed changes in the transcription of endothelial gene sets linked to the endothelial phenotype and in chromatin accessibility around ERG-binding sites. Mechanistically, LINC00607 interacted with the SWI/SNF chromatin remodeling protein BRG1. CRISPR/Cas9-mediated knockout of BRG1 in HUVEC followed by CUT&RUN revealed that BRG1 is required to secure a stable chromatin state, mainly on ERG-binding sites. In conclusion, LINC00607 is an endothelial-enriched lncRNA that maintains ERG target gene transcription by interacting with the chromatin remodeler BRG1 to ultimately mediate angiogenesis.

Indexed as

RNA, Long NoncodingAnimalsChromatinDNA HelicasesEndothelial CellsHumansMiceMice, SCIDNeovascularization, PhysiologicNuclear ProteinsChromatinDNA HelicasesNuclear ProteinsRNA, Long NoncodingBRG1Endothelial cellERGGene regulationHypoxiaLong non-coding RNA

Identifiers

PMID36700983
PMCPMC9879848
OpenAlexW4318066573

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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.