Evidence map›Paper›PMID 42624953›Full record

ReviewAngiogenesis2026

Pathogenesis and molecular mechanisms of mutant TIE2-driven venous malformation.

Lindsay J Bischoff, Elisa Boscolo

Abstract readReview
In one paragraph

Review in Angiogenesis, 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
–field-weighted citation impact
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

2 authors.

Lindsay J BischoffDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA.
Elisa BoscoloDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH, 45229, USA. elisa.boscolo@cchmc.org.ORCID https://orcid.org/0000-0002-6996-0419

Funding

Venous Malformations (VM): A Murine Model to Identify Therapies to Target AberranR01HL117952 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI BOSCOLO, ELISA · 2013 to 2025
$4.9M
Pathogenesis of Vascular Anomalies with GNAQ mutationsR01HL167700 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI ELISA BOSCOLO · 2024 to 2026
$1.8M
The Role of c-ABL in Mediating TIE2 Signaling and Formation of Venous MalformationF31HL176101 · NHLBI · UNIVERSITY OF CINCINNATI · PI BISCHOFF, LINDSAY · 2024 to 2025
$93k
NHLBI NIH HHS F31 HL176101NHLBI NIH HHS F31HL176101NHLBI NIH HHS R01 HL117952NHLBI NIH HHS R01HL117952NHLBI NIH HHS R01 HL167700
6 · The paper itself

Abstract

Venous malformation (VM) is the most common subtype of vascular malformation. Due to the chronic nature of this disorder, VM patients face significant morbidity and complications throughout their lives. Current therapeutic options can be limited, but recent advances in understanding the cellular and molecular mechanisms that underly VM pathogenesis provide hope for the discovery of more effective targeted therapies. These advances arise from a greater understanding of the cellular effects of VM-causative mutations, which has been aided by the development of more advanced and physiologically relevant model systems. In this review, we begin by providing a brief overview of the clinical characteristics and genetic driver mutations of the most common subtypes of all vascular anomalies (including vascular tumors and vascular malformations), providing context for our more detailed discussion of these aspects of VM. We further summarize the current treatment options available for VM patients and the advancements that have been made in the use of targeted therapies for these patients. We further discuss recent advances in the development of model systems that can be used to study VM pathogenesis. Finally, we focus this review on the mechanisms that are downstream of mutant TIE2, discussing structural features of the receptor, TIE2 signaling pathways, and its roles in vascular physiology and VM pathology.

Indexed as

MutationReceptor, TIE-2Vascular MalformationsVeinsAnimalsHumansSignal TransductionReceptor, TIE-2TEK protein, humanPIK3CATIE2Vascular anomalyVenous malformation

Identifiers

PMID42624953
PMCPMC13493436

What OpenQuestion holds

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Registered trials

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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.