Evidence map›Paper›PMID 30604758›Full record

ArticleNature communications2019

Endovascular progenitors infiltrate melanomas and differentiate towards a variety of vascular beds promoting tumor metastasis.

Prudence Donovan, Jatin Patel, James Dight, Ho Yi Wong, Seen-Ling Sim, Valentine Murigneux, Mathias Francois, Kiarash Khosrotehrani

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  11. Alk1 acts in non-endothelial VE-cadherinNature communications · 2023
    Article
  12. Article
  13. Review
  14. The Role of Hedgehog Signaling in the Melanoma Tumor Bone Microenvironment.International journal of molecular sciences · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. MyeloidFrontiers in endocrinology · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Prudence DonovanTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia.
Jatin PatelTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia. j.patel@uq.edu.au.ORCID http://orcid.org/0000-0002-3511-0029
James DightTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia.
Ho Yi WongTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia.
Seen-Ling SimTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia.
Valentine MurigneuxTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia.
Mathias FrancoisInstitute of Molecular Biosciences, The University of Queensland, Brisbane, 4072, QLD, Australia.
Kiarash KhosrotehraniTranslational Research Institute, UQ Diamantina Institute, The University of Queensland, Brisbane, 4102, QLD, Australia. k.khosrotehrani@uq.edu.au.
Translational Research Institute · AUThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor vascularization is a hallmark of cancer central to disease progression and metastasis. Current anti-angiogenic therapies have limited success prompting the need to better understand the cellular origin of tumor vessels. Using fate-mapping analysis of endothelial cell populations in melanoma, we report the very early infiltration of endovascular progenitors (EVP) in growing tumors. These cells harbored self-renewal and reactivated the expression of SOX18 transcription factor, initiating a vasculogenic process as single cells, progressing towards a transit amplifying stage and ultimately differentiating into more mature endothelial phenotypes that comprised arterial, venous and lymphatic subtypes within the core of the tumor. Molecular profiling by RNA sequencing of purified endothelial fractions characterized EVPs as quiescent progenitors remodeling the extracellular matrix with significant paracrine activity promoting growth. Functionally, EVPs did not rely on VEGF-A signaling whereas endothelial-specific loss of Rbpj depleted the population and strongly inhibited metastasis. The understanding of endothelial heterogeneity opens new avenues for more effective anti-vascular therapies in cancer.

Indexed as

AnimalsCell DifferentiationCell Line, TumorCell Transformation, NeoplasticEndothelial Progenitor CellsEndothelium, VascularExtracellular MatrixFemaleImmunoglobulin J Recombination Signal Sequence-Binding ProteinLymphatic VesselsMaleMelanoma, ExperimentalMiceMice, Inbred C57BLMice, TransgenicNeoplasm InvasivenessImmunoglobulin J Recombination Signal Sequence-Binding ProteinRbpj protein, mouseSox18 protein, mouseSOXF Transcription FactorsVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID30604758
PMCPMC6318267
OpenAlexW2907613123

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.