Evidence map›Paper›PMID 11958368›Full record

ArticleBrain pathology (Zurich, Switzerland)2002

Allelic gain and amplification on the long arm of chromosome 17 in anaplastic meningiomas.

Rainer Büschges, Koichi Ichimura, Ruthild G Weber, Guido Reifenberger, V Peter Collins

Open access · greenAbstract readComparative Study
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Molecular characteristics of meningiomas.Journal of pathology and translational medicine · 2020
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Update on meningiomas.The oncologist · 2011
    Review
  11. Article
  12. Article
  13. Molecular biology of unreresectable meningiomas: implications for new treatments and review of the literature.Skull base : official journal of North American Skull Base Society ... [et al.] · 2008
    Article
  14. Article
  15. Article
  16. Molecular pathogenesis of meningiomas.Journal of neuro-oncology · 2004
    Review
  17. Brain tumours: classification and genes.Journal of neurology, neurosurgery, and psychiatry · 2004
    Review
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 4 institutions in 2 countries.

Rainer BüschgesDepartment of Pathology, University of Cambridge, Addenbrooke's Hospital, United Kingdom.
Koichi Ichimura
Ruthild G Weber
Guido Reifenberger
V Peter Collins
Addenbrooke's Hospital · GBHeidelberg University · DEHeinrich Heine University Düsseldorf · DEUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using comparative genomic hybridization (CGH) we have previously identified amplification at 17q21-qter as a common aberration in anaplastic meningiomas but not in atypical or benign meningiomas (19). To define the amplified genomic region, we analyzed 44 meningeal tumors, including 7 benign meningiomas of World Health Organization (WHO) grade 1,19 atypical meningiomas (WHO grade II) and 18 anaplastic meningiomas (WHO grade III) at 46 chromosome 17 loci (including 42 17q loci). In line with the CGH data we found evidence of increased numbers of alleles on 17q. The incidence rose with malignancy grade, culminating at 61% (11 of 18 cases) in the anaplastic meningioma group. The majority of cases showing increased allele numbers had, on average, low-level allelic gains (relative increase in allele dosage of 2- to 5-fold). Amplification of alleles (defined here as an average relative increase in allele dosage of more than 5 times) was detected in 2 anaplastic meningiomas. The amplification patterns in these tumors defined a number of common regions of amplification/increased allele copy number, the best defined include one between D17S790 and D17S1607 and one between D17S1160 and PS6K. Real-time PCR analysis of the PS6K candidate gene revealed no high-level amplification despite this affecting adjacent loci. Our findings are fundamental for the identification of the gene(s) in 17q22-q23 that is (are) the target(s) for increased copy number in anaplastic meningiomas and possibly other tumor types.

Indexed as

AllelesGene AmplificationAdolescentAdultAgedAged, 80 and overChildChromosomes, Human, Pair 17FemaleHumansMaleMeningeal NeoplasmsMeningiomaMicrosatellite RepeatsMiddle AgedNucleic Acid HybridizationRibosomal Protein S6 Kinases

Identifiers

PMID11958368
PMCPMC8095877
OpenAlexW2024135467

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.