Evidence map›Paper›PMID 41935951›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2026

LINC00607 facilitates endothelial VEGF-A receptor FLT1 splicing.

Frederike Lam, Timothy Warwick, James A Oo, Agnes Y Krüger, Nina-Naomi Kreis, Anastasiia Diagel, Judit Izquierdo Ponce, Praveenya Tirunagari, Marie E Bayer, Olivia Nonn and 11 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Frederike LamGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany; German Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Timothy WarwickGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany; German Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
James A OoGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany; German Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Agnes Y KrügerGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany.
Nina-Naomi KreisGoethe University, University Hospital Frankfurt, Division of Obstetrics and Prenatal Medicine, Frankfurt, Germany.
Anastasiia DiagelTechnical University of Munich, Department of Cardiology, German Heart Centre Munich, School of Medicine and Health, Munich, Germany; DZHK, Partner Site Munich Heart Alliance, Munich, Germany.
Judit Izquierdo PonceGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany.
Praveenya TirunagariGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany.
Marie E BayerGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany.
Olivia NonnCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany; DZHK, Berlin, Germany.
Ralf DechendCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany; DZHK, Berlin, Germany; HELIOS Klinikum Berlin-Buch, Department of Cardiology and Nephrology, Berlin, Germany.
Thomas WaltherGoethe University, University Hospital Frankfurt, Department of Cardiovascular Surgery, Frankfurt, Germany.
Reinier A BoonGerman Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany; Goethe University, Institute for Cardiovascular Regeneration, Centre for Molecular Medicine, Frankfurt, Germany; Department of Physiology, Amsterdam Cardiovascular Sciences, VU Medical Center, Amsterdam UMC, Amsterdam, the Netherlands.
Andrew H BakerInstitute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh, Scotland; CARIM Institute, University of Maastricht, Maastricht, the Netherlands.
Stefan GüntherMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.
Ilka WittigGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany; German Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Zhifen ChenTechnical University of Munich, Department of Cardiology, German Heart Centre Munich, School of Medicine and Health, Munich, Germany; DZHK, Partner Site Munich Heart Alliance, Munich, Germany.
Michaela Müller-McNicollGoethe University Frankfurt, Institute for Molecular Biosciences, Frankfurt, Germany; Max Planck Institute for Biophysics, Frankfurt, Germany.
Frank LouwenGoethe University, University Hospital Frankfurt, Division of Obstetrics and Prenatal Medicine, Frankfurt, Germany.
Ralf P BrandesGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany; German Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany.
Matthias S LeisegangGoethe University, Institute for Cardiovascular Physiology, Frankfurt, Germany; German Center of Cardiovascular Research (DZHK), Partner Site RheinMain, Frankfurt, Germany. Electronic address: leisegang@vrc.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is a key function of vascular endothelial cells and becomes aberrant in pathologies such as preeclampsia. An important mediator of angiogenesis is vascular endothelial growth factor (VEGF) receptor FLT1; however, alternative splicing of FLT1 can generate soluble FLT1 (sFLT1), a decoy receptor that inhibits VEGF signaling. While some long non-coding RNAs (lncRNAs) are known to regulate splicing, their roles in endothelial biology remain poorly defined. Here, we identify lncRNA LINC00607 as a critical regulator of FLT1 alternative splicing. Loss of LINC00607 increased the formation of the anti-angiogenic sFLT1. CRISPR-mediated knockout of LINC00607 promoted exon 15 inclusion in FLT1, elevating sFLT1 levels and blunting VEGF-driven angiogenesis-a defect reversed by sFLT1-neutralizing antibodies. LINC00607 interacted with U2 small nuclear RNA (snRNA) to regulate exon 15 inclusion in FLT1, an interaction dependent on the chromatin-remodeler BRG1. A splice-blocking morpholino targeting the FLT1 intron14/exon15 junction specifically inhibited sFLT1 production by interacting with LINC00607 and U2 snRNA, and its application increased VEGF-A-mediated sprouting. LINC00607 expression inversely correlated with sFLT1 levels in vascular diseases. In preeclampsia, a multisystem pregnancy disorder involving hypertension and proteinuria, LINC00607 was downregulated in early and late-stage preeclampsia compared with healthy pregnancies. LINC00607 therefore fine-tunes VEGF signaling and might contribute to the pathophysiology of preeclampsia.

Indexed as

Alternative SplicingRNA, Long NoncodingVascular Endothelial Growth Factor Receptor-1AngiogenesisAnimalsExonsFemaleGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsPre-EclampsiaPregnancySignal TransductionVascular Endothelial Growth Factor AFLT1 protein, humanRNA, Long NoncodingVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1angiogenesisLINC00607long non-coding RNAmorpholinopreeclampsiasFLT1soluble FMS-like tyrosine kinase-1splicingvascular endothelial growth factorVEGF

Identifiers

PMID41935951
PMCPMC13330067

What OpenQuestion holds

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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.