Evidence map›Paper›PMID 30717262›Full record

ReviewInternational journal of molecular sciences2019

Neuropilins in the Context of Tumor Vasculature.

Stephan Niland, Johannes A Eble

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
5.2field-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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 90 citations in OpenAlex.

  1. Pooled it
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  10. Frontiers in pharmacology · 2024
    Article
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  18. Advances in SEMA3F regulation of clinically high-incidence cancers.Cancer biomarkers : section A of Disease markers · 2023
    Article
  19. Review
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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 at 1 institution in 1 country.

Stephan NilandInstitute of Physiological Chemistry and Pathobiochemistry, University of Münster, 48149 Münster, Germany. nilands@uni-muenster.de.ORCID 0000-0002-2055-8656
Johannes A EbleInstitute of Physiological Chemistry and Pathobiochemistry, University of Münster, 48149 Münster, Germany. johannes.eble@uni-muenster.de.ORCID 0000-0001-9156-2137
University of Münster · DE

Funding

Deutsche Forschungsgemeinschaft SFB1009 A09
6 · The paper itself

Abstract

Neuropilin-1 and Neuropilin-2 form a small family of plasma membrane spanning receptors originally identified by the binding of semaphorin and vascular endothelial growth factor. Having no cytosolic protein kinase domain, they function predominantly as co-receptors of other receptors for various ligands. As such, they critically modulate the signaling of various receptor tyrosine kinases, integrins, and other molecules involved in the regulation of physiological and pathological angiogenic processes. This review highlights the diverse neuropilin ligands and interacting partners on endothelial cells, which are relevant in the context of the tumor vasculature and the tumor microenvironment. In addition to tumor cells, the latter contains cancer-associated fibroblasts, immune cells, and endothelial cells. Based on the prevalent neuropilin-mediated interactions, the suitability of various neuropilin-targeted substances for influencing tumor angiogenesis as a possible building block of a tumor therapy is discussed.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBinding SitesCancer-Associated FibroblastsEndothelial CellsHumansLigandsNeoplasmsNeovascularization, PathologicNeuropilin-1Neuropilin-2Protein BindingProtein Interaction Domains and MotifsSemaphorinsSignal TransductionTumor MicroenvironmentLigandsNeuropilin-1Neuropilin-2neuropilin-2, humanNRP1 protein, humanSemaphorinsVascular Endothelial Growth Factor AVEGFA protein, humanendothelial cellneuropilin interaction partnersneuropilin ligandsneuropilin signalingsemaphorintumor angiogenesistumor microenvironmenttumor-penetrating peptidestumor vasculaturevascular endothelial growth factor

Identifiers

PMID30717262
PMCPMC6387129
OpenAlexW2911832706

What Socratic 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 Socratic graph.