Evidence map›Paper›PMID 23099891›Full record

ArticleActa neuropathologica2013

Neurofibroma-associated macrophages play roles in tumor growth and response to pharmacological inhibition.

Carlos E Prada, Edwin Jousma, Tilat A Rizvi, Jianqiang Wu, R Scott Dunn, Debra A Mayes, Jose A Cancelas, Eva Dombi, Mi-Ok Kim, Brian L West and 2 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Acta neuropathologica, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 94 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 1 pooled it
4.5field-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.

NCT03231306 phase2completednot on this mapstarted 2017, after this paper: background citation

A Phase II Study of Binimetinib in Children and Adults With NF1 Associated Plexiform Neurofibromas (PNOC010)

TypeinterventionalSponsorUniversity of Alabama at BirminghamRan2017 to 2024Enrolled45ConditionsNeurofibromatosis Type 1, Plexiform NeurofibromaArmsBinimetinib
NCT05238909 enrolling by invitationnot on this mapstarted 2022, after this paper: background citation

Developing Novel Biomarkers of Plexiform Neurofibroma Tumor Burden

Typeobservational_patient_registrySponsorAnn & Robert H Lurie Children's Hospital of ChicagoRan2022 to 2027Enrolled200ConditionsNeurofibromatosis 1, NF1, Neurofibromatosis Type 1
3 · Its place in the literature

Who cites it

94 citing papers in PubMed, 1 synthesis or guideline pooled it, 140 citations in OpenAlex.

  1. Pooled it
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  6. Extracellular vesicles in spine tumors: biological roles, immune modulation, and therapeutic implications.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
    Review
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34 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

12 authors at 3 institutions in 1 country.

Carlos E PradaDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.
Edwin Jousma
Tilat A Rizvi
Jianqiang Wu
R Scott Dunn
Debra A Mayes
Jose A Cancelas
Eva Dombi
Mi-Ok Kim
Brian L West
Gideon Bollag
Nancy Ratner
Cincinnati Children's Hospital Medical Center · USPlexxikon (United States)National Cancer Institute · US

Funding

MITOGENIC ACTIVITIES IN NEUROFIBROMATOSISR01NS028840 · NINDS · UNIVERSITY OF CINCINNATI · PI NANCY RATNER · 1990 to 2026
$10.1M
Xenograft Core for NF1 Experimental TherapeuticsP50NS057531 · NINDS · CINCINNATI CHILDRENS HOSP MED CTR · PI RATNER, NANCY · 2008 to 2012
$6.8M
Training Program in Cancer TherapeuticsT32CA117846 · NCI · UNIVERSITY OF CINCINNATI · PI PRICE, CAROLYN M, TAKIAR, VINITA · 2006 to 2022
$6.5M
NCI NIH HHS T32 CA117846NINDS NIH HHS NS28840NINDS NIH HHS P50 NS057531NINDS NIH HHS P50-NS057531NINDS NIH HHS R01 NS028840
6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is a common genetic disease that predisposes 30-50 % of affected individuals to develop plexiform neurofibromas. We found that macrophage infiltration of both mouse and human neurofibromas correlates with disease progression. Macrophages accounted for almost half of neurofibroma cells, leading us to hypothesize that nerve macrophages are inflammatory effectors in neurofibroma development and/or growth. We tested the effects of PLX3397, a dual kit/fms kinase inhibitor that blocks macrophage infiltration, in the Dhh-Cre; Nf1(flox/flox) mouse model of GEM grade I neurofibroma. In mice aged 1-4 months, prior to development of nerve pathology and neurofibroma formation, PLX3397 did not impair tumor initiation and increased tumor volume compared to controls. However, in mice aged 7-9 months, after tumor establishment, a subset of mice demonstrating the largest reductions in macrophages after PLX3397 exhibited cell death and tumor volume regression. Macrophages are likely to provide an initial line of defense against developing tumors. Once tumors are established, they become tumor permissive. Macrophage depletion may result in impaired tumor maintenance and represent a therapeutic strategy for neurofibroma therapy.

Indexed as

Age FactorsAnimalsDisease Models, AnimalEnzyme InhibitorsHumansMacrophagesMiceMice, 129 StrainMice, Inbred C57BLMice, TransgenicNeurofibromaNeurofibromin 1NeuronsSchwann CellsTumor BurdenEnzyme InhibitorsNeurofibromin 1

Identifiers

PMID23099891
PMCPMC3547628
OpenAlexW2079659068

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.