Evidence map›Paper›PMID 30101525›Full record

ArticleThe Journal of pathology2018

Targeting PDGF-mediated recruitment of pericytes blocks vascular mimicry and tumor growth.

Victor Ljl Thijssen, Yvette Wj Paulis, Patrycja Nowak-Sliwinska, Katrin L Deumelandt, Kayoko Hosaka, Patricia Mmb Soetekouw, Anca M Cimpean, Marius Raica, Patrick Pauwels, Joost J van den Oord and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

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  15. Vascular Remodeling: The Multicellular Mechanisms of Pulmonary Hypertension.International journal of molecular sciences · 2025
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4 more citing papers are in PubMed but not listed here.

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

15 authors at 9 institutions in 6 countries.

Victor Ljl ThijssenAngiogenesis Laboratory, Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Yvette Wj PaulisAngiogenesis Laboratory, Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Patrycja Nowak-SliwinskaAngiogenesis Laboratory, Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Katrin L DeumelandtAngiogenesis Laboratory, Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Kayoko HosakaDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden.
Patricia Mmb SoetekouwDivision of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.
Anca M CimpeanDepartment of Microscopic Morphology, Histology, Angiogenesis Research Center, Victor Babes University of Medicine and Pharmacy, Timisoara, Romania.
Marius RaicaDepartment of Microscopic Morphology, Histology, Angiogenesis Research Center, Victor Babes University of Medicine and Pharmacy, Timisoara, Romania.
Patrick PauwelsDepartment of Pathology, Antwerp University Hospital, Edegem, Belgium.
Joost J van den OordLaboratory of Translational Cell and Tissue Research, University of Leuven, Leuven, Belgium.
Vivianne Cg Tjan-HeijnenDivision of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.
Mary J HendrixDepartment of Biology, Shepherd University, Shepherdstown University, WV, USA.
Carl-Henrik HeldinDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Yihai CaoDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden.
Arjan W GriffioenAngiogenesis Laboratory, Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0002-8508-4754
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLMaastricht University · NLKarolinska Institutet · SEVictor Babeș University of Medicine and Pharmacy Timișoara · ROAntwerp University Hospital · BEKU Leuven · BEShepherd University · USUniversity of Geneva · CHUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aggressive tumor cells can adopt an endothelial cell-like phenotype and contribute to the formation of a tumor vasculature, independent of tumor angiogenesis. This adoptive mechanism is referred to as vascular mimicry and it is associated with poor survival in cancer patients. To what extent tumor cells capable of vascular mimicry phenocopy the angiogenic cascade is still poorly explored. Here, we identify pericytes as important players in vascular mimicry. We found that pericytes are recruited by vascular mimicry-positive tumor cells in order to facilitate sprouting and to provide structural support of the vascular-like networks. The pericyte recruitment is mediated through platelet-derived growth factor (PDGF)-B. Consequently, preventing PDGF-B signaling by blocking the PDGF receptors with either the small tyrosine kinase inhibitor imatinib or blocking antibodies inhibits vascular mimicry and tumor growth. Collectively, the current study identifies an important role for pericytes in the formation of vascular-like structures by tumor cells. Moreover, the mechanism that controls the pericyte recruitment provides therapeutic opportunities for patients with aggressive vascular mimicry-positive cancer types. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

Neovascularization, PathologicAnimalsAntineoplastic Agents, ImmunologicalBiological MimicryCell CommunicationCell Line, TumorCell ProliferationCoculture TechniquesHumansImatinib MesylateMelanoma, ExperimentalMiceMice, NudePericytesPlatelet-Derived Growth FactorProtein Kinase InhibitorsAntineoplastic Agents, ImmunologicalImatinib MesylatePlatelet-Derived Growth FactorProtein Kinase Inhibitorscancerendothelial cellsEwing sarcomaimatinibmelanomaperivascular cellstumor angiogenesisvasculogenic mimicryvessel stabilization

Identifiers

PMID30101525
PMCPMC6587443
OpenAlexW2887920087

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.