Evidence map›Paper›PMID 30479396›Full record

ArticleNature communications2018

NF1 heterozygosity fosters de novo tumorigenesis but impairs malignant transformation.

Jean-Philippe Brosseau, Chung-Ping Liao, Yong Wang, Vijay Ramani, Travis Vandergriff, Michelle Lee, Amisha Patel, Kiyoshi Ariizumi, Lu Q Le

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.8field-weighted citation impact, top 5% 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, 55 citations in OpenAlex.

  1. Article
  2. Clinical characteristics and treatment strategies of brainstem lesion in children with neurofibromatosis type 1.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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  14. TheCancers · 2024
    Review
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  18. Review
  19. Review
  20. Evaluation of NF1 and RASA1 gene expression in endometriosis.European journal of obstetrics & gynecology and reproductive biology: X · 2022
    Article
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

9 authors at 2 institutions in 1 country.

Jean-Philippe BrosseauDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Chung-Ping LiaoDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Yong WangDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Vijay RamaniDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Travis VandergriffDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Michelle LeeDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Amisha PatelDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Kiyoshi AriizumiDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Lu Q LeDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA. lu.le@utsouthwestern.edu.ORCID http://orcid.org/0000-0003-2817-5382
The University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

Project 4: Secondary Cancers Among NF1 Cancer SurvivorsU54CA196519 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI Yunlong Liu · 2015 to 2026
$26.9M
Transcriptional Function of Krox20 in Development and TumorigenesisR01CA166593 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI LE, LU · 2012 to 2022
$3.7M
NCI NIH HHS R01 CA166593NCI NIH HHS U54 CA196519
6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is an autosomal genetic disorder. Patients with NF1 are associated with mono-allelic loss of the tumor suppressor gene NF1 in their germline, which predisposes them to develop a wide array of benign lesions. Intriguingly, recent sequencing efforts revealed that the NF1 gene is frequently mutated in multiple malignant tumors not typically associated with NF1 patients, suggesting that NF1 heterozygosity is refractory to at least some cancer types. In two orthogonal mouse models representing NF1- and non-NF1-related tumors, we discover that an Nf1

Indexed as

AnimalsCarcinogenesisCell ProliferationCell Transformation, NeoplasticDisease Models, AnimalDisease ProgressionHeterozygoteHumansKeratinocytesMice, Inbred C57BLNeurofibromaNeurofibromin 1PhenotypeSkin NeoplasmsT-LymphocytesTumor MicroenvironmentNeurofibromin 1

Identifiers

PMID30479396
PMCPMC6258697
OpenAlexW2901551339

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.