Evidence map›Paper›PMID 31591222›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Molecular profiling predicts meningioma recurrence and reveals loss of DREAM complex repression in aggressive tumors.

Akash J Patel, Ying-Wooi Wan, Rami Al-Ouran, Jean-Pierre Revelli, Maria F Cardenas, Mazen Oneissi, Liu Xi, Ali Jalali, John F Magnotti, Donna M Muzny and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 136 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
136citing papers in PubMed, 2 pooled it
12.1field-weighted citation impact, top 1% 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

136 citing papers in PubMed, 2 syntheses or guidelines pooled it, 194 citations in OpenAlex.

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  16. Rational Radionuclide Therapy for Recurrent Meningioma.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
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76 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

22 authors at 3 institutions in 1 country.

Akash J PatelDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.ORCID 0000-0002-1280-2989
Ying-Wooi WanJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030; yingwoow@bcm.edu hzoghbi@bcm.edu klisch@bcm.edu.
Rami Al-OuranJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030.
Jean-Pierre RevelliJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030.
Maria F CardenasHuman Genome Sequencing Center, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.
Mazen OneissiDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.
Liu XiHuman Genome Sequencing Center, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.
Ali JalaliDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.
John F MagnottiDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.ORCID 0000-0003-2093-0603
Donna M MuznyHuman Genome Sequencing Center, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.
HarshaVardhan DoddapaneniHuman Genome Sequencing Center, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.
Sherly SebastianDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.
Kent A HeckDepartment of Pathology, Baylor College of Medicine, Houston, TX 77030.
J Clay GoodmanDepartment of Pathology, Baylor College of Medicine, Houston, TX 77030.
Shankar P GopinathDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.
Zhandong LiuJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030.ORCID 0000-0002-7608-0831
Ganesh RaoDepartment of Neurosurgery, University of Texas MD Anderson Cancer Center, Houston, TX 77030.
Sharon E PlonDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.ORCID 0000-0002-9626-0936
Daniel YoshorDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX 77030.
David A WheelerHuman Genome Sequencing Center, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.
Huda Y ZoghbiJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030; yingwoow@bcm.edu hzoghbi@bcm.edu klisch@bcm.edu.
Tiemo J KlischJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030; yingwoow@bcm.edu hzoghbi@bcm.edu klisch@bcm.edu.ORCID 0000-0001-8182-384X
Baylor College of Medicine · USHoward Hughes Medical Institute · USThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Establishing the Genomic Landscape of Human Atypical MeningiomasK08NS102474 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI PATEL, AKASH J. · 2017 to 2021
$869k
Howard Hughes Medical InstituteNCI NIH HHS P30 CA016672NCI NIH HHS P30 CA125123NINDS NIH HHS K08 NS102474
6 · The paper itself

Abstract

Meningiomas account for one-third of all primary brain tumors. Although typically benign, about 20% of meningiomas are aggressive, and despite the rigor of the current histopathological classification system there remains considerable uncertainty in predicting tumor behavior. Here, we analyzed 160 tumors from all 3 World Health Organization (WHO) grades (I through III) using clinical, gene expression, and sequencing data. Unsupervised clustering analysis identified 3 molecular types (A, B, and C) that reliably predicted recurrence. These groups did not directly correlate with the WHO grading system, which classifies more than half of the tumors in the most aggressive molecular type as benign. Transcriptional and biochemical analyses revealed that aggressive meningiomas involve loss of the repressor function of the DREAM complex, which results in cell-cycle activation; only tumors in this category tend to recur after full resection. These findings should improve our ability to predict recurrence and develop targeted treatments for these clinically challenging tumors.

Indexed as

AdultAgedAged, 80 and overCell CycleCell LineDisease ProgressionDNA Copy Number VariationsFemaleGene Expression ProfilingHumansKv Channel-Interacting ProteinsMaleMeningeal NeoplasmsMeningiomaMiddle AgedNeoplasm Recurrence, LocalKCNIP3 protein, humanKv Channel-Interacting ProteinsRepressor Proteinsbrain tumorclassificationNF2oncogenesisPRC2

Identifiers

PMID31591222
PMCPMC6815170
OpenAlexW2980193786

What OpenQuestion holds

Textmetadata
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.