Evidence map›Paper›PMID 21157382›Full record

ArticleJournal of neuropathology and experimental neurology2011

Identification of gene markers associated with aggressive meningioma by filtering across multiple sets of gene expression arrays.

Jourdan E Stuart, Eriks A Lusis, Adrienne C Scheck, Stephen W Coons, Anita Lal, Arie Perry, David H Gutmann

Abstract readComparative Study
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  4. Article
  5. Review
  6. Article
  7. Beyond the WHO classification of meningioma: using molecular diagnostics to guide management.Advances in clinical neuroscience & rehabilitation : ACNR · 2023
    Article
  8. Article
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  14. Prognostic value of DLGAP5 in colorectal cancer.International journal of colorectal disease · 2019
    Article
  15. Article
  16. SOX11: friend or foe in tumor prevention and carcinogenesis?Therapeutic advances in medical oncology · 2019
    Review
  17. Article
  18. Article
  19. Article
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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

7 authors.

Jourdan E StuartDepartment of Neurology, Washington University School of Medicine, St Louis, Missouri 63110, USA.
Eriks A Lusis
Adrienne C Scheck
Stephen W Coons
Anita Lal
Arie Perry
David H Gutmann

Funding

Tissue CoreP50CA097257 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2002 to 2026
$57.4M
NCI NIH HHS P50 CA097257NCI NIH HHS P50CA097257
6 · The paper itself

Abstract

Meningiomas are common intracranial tumors, but relatively little is known about the genetic events responsible for their clinical diversity. Although recent genomic studies have provided clues, the genes identified often differ among publications. We used microarray expression profiling to identify genes that are differentially expressed, with at least a 4-fold change, between grade I and grade III meningiomas. We filtered this initial set of potential biomarkers through a second cohort of meningiomas and then verified the remaining genes by quantitative polymerase chain reaction followed by examination using a third microarray expression cohort. Using this approach, we identified 9 overexpressed (TPX2, RRM2, TOP2A, PI3, BIRC5, CDC2, NUSAP1, DLG7, SOX11) and 2 underexpressed (TIMP3, KCNMA1) genes in grade III versus grade I meningiomas. As a further validation step, we analyzed these genes in a fourth cohort and found that patients with grade II meningiomas with high topoisomerase 2-α protein expressions (>5% labeling index) had shorter times to death than patients with low expressions. We believe that this multistep multi-cohort approach provides a robust method for reducing false-positives while generating a list of reproducible candidate genes that are associated with clinically aggressive meningiomas and are suitable for analysis for their potential prognostic value.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAged, 80 and overCohort StudiesFemaleGene Expression ProfilingGenetic MarkersHumansMaleMeningeal NeoplasmsMeningiomaMiddle AgedNeoplasm ProteinsGenetic MarkersNeoplasm Proteins

Identifiers

PMID21157382
PMCPMC3839953

What OpenQuestion holds

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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.