Evidence map›Paper›PMID 26465118›Full record

ReviewMicrocirculation (New York, N.Y. : 1994)2016

NG2 Proteoglycan-Dependent Contributions of Pericytes and Macrophages to Brain Tumor Vascularization and Progression.

William B Stallcup, Weon-Kyoo You, Karolina Kucharova, Pilar Cejudo-Martin, Fusanori Yotsumoto

Abstract readReview
In one paragraph

Review in Microcirculation (New York, N.Y. : 1994), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 47 citations in OpenAlex.

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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

5 authors at 2 institutions in 3 countries.

William B StallcupSanford Burnham Prebys Medical Discovery Institute, Cancer Center, La Jolla, California, USA.
Weon-Kyoo YouSanford Burnham Prebys Medical Discovery Institute, Cancer Center, La Jolla, California, USA.
Karolina KucharovaSanford Burnham Prebys Medical Discovery Institute, Cancer Center, La Jolla, California, USA.
Pilar Cejudo-MartinSanford Burnham Prebys Medical Discovery Institute, Cancer Center, La Jolla, California, USA.
Fusanori YotsumotoSanford Burnham Prebys Medical Discovery Institute, Cancer Center, La Jolla, California, USA.
Sanford Burnham Prebys Medical Discovery Institute · USDiscovery Institute · US

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI ELENA B PASQUALE · 1985 to 2026
$107.2M
NG2-PG in tumor vascularization and progressionR01CA095287 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI STALLCUP, WILLIAM B. · 2002 to 2016
$5.3M
NCI NIH HHS NIH P30 CA030199NCI NIH HHS NIH R01 CA095287NCI NIH HHS P30 CA030199NCI NIH HHS R01 CA095287
6 · The paper itself

Abstract

The NG2 proteoglycan promotes tumor growth as a component of both tumor and stromal cells. Using intracranial, NG2-negative B16F10 melanomas, we have investigated the importance of PC and Mac NG2 in brain tumor progression. Reduced melanoma growth in Mac-NG2ko and PC-NG2ko mice demonstrates the importance of NG2 in both stromal compartments. In each genotype, the loss of PC-endothelial cell interaction diminishes the formation of endothelial junctions and assembly of the basal lamina. Tumor vessels in Mac-NG2ko mice have smaller diameters, reduced patency, and increased leakiness compared to PC-NG2ko mice, thus decreasing tumor blood supply and increasing hypoxia. While the reduced PC interaction with endothelial cells in PC-NG2ko mice results from the loss of PC activation of β1 integrin signaling in endothelial cells, reduced PC-endothelial cell interaction in Mac-NG2ko mice results from 90% reduced Mac recruitment. The absence of Mac-derived signals in Mac-NG2ko mice causes the loss of PC association with endothelial cells. Reduced Mac recruitment may be due to diminished activation of integrins in the absence of NG2, causing decreased Mac interaction with endothelial adhesion molecules that are needed for extravasation. These results reflect the complex interplay that occurs between Mac, PC, and endothelial cells during tumor vascularization.

Indexed as

AnimalsAntigensBrain NeoplasmsChondroitin Sulfate Proteoglycan 4MacrophagesMiceMice, KnockoutNeoplasm ProteinsNeovascularization, PathologicPericytesProteoglycansAntigensChondroitin Sulfate Proteoglycan 4Neoplasm ProteinsProteoglycansmacrophage recruitmentneuron-glia antigen 2 proteoglycanpericyte-endothelial cell interactiontumor growthtumor microenvironmenttumor vascularization

Identifiers

PMID26465118
PMCPMC4744154
OpenAlexW2183578062

What OpenQuestion holds

Textmetadata
LicenceTDM
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.