Evidence map›Paper›PMID 10668898›Full record

ArticleBrain pathology (Zurich, Switzerland)2000

Low frequency of SV40, JC and BK polyomavirus sequences in human medulloblastomas, meningiomas and ependymomas.

S Weggen, T A Bayer, A von Deimling, G Reifenberger, D von Schweinitz, O D Wiestler, T Pietsch

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Role of BK human polyomavirus in cancer.Infectious agents and cancer · 2018
    Review
  7. Review
  8. Review
  9. Medulloblastoma-biology and microenvironment: a review.Pediatric hematology and oncology · 2012
    Review
  10. Review
  11. Chronic viral infection and primary central nervous system malignancy.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2010
    Review
  12. Review
  13. Article
  14. Potential mechanisms of the human polyomavirus JC in neural oncogenesis.Journal of neuropathology and experimental neurology · 2008
    Review
  15. Article
  16. High prevalence of human polyomavirus JC VP1 gene sequences in pediatric malignancies.Cellular and molecular biology (Noisy-le-Grand, France) · 2007
    Article
  17. Article
  18. Article
  19. Immunolocalization of caveolin-1 in rat and human mesothelium.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2004
    Article
  20. Molecular pathogenesis of childhood brain tumors.Journal of neuro-oncology · 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

7 authors at 3 institutions in 2 countries.

S WeggenDepartment of Neuropathology, University of Bonn Medical Center, Germany.
T A Bayer
A von Deimling
G Reifenberger
D von Schweinitz
O D Wiestler
T Pietsch
University of Bonn · DEMedizinische Hochschule Hannover · DETranslational Research in Oncology · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several reports have suggested a role for polyomaviruses in the pathogenesis of human brain tumors. This potential involvement is not conclusively resolved. For the present study, a highly sensitive PCR-assay with fluorescence-labelled primers was developed to search for polyomavirus sequences in human brain tumor and control DNA samples. The assay was shown to detect approximately one viral large T-antigen (TAg) gene per 250 cells. We identified simian virus 40 (SV40)-like sequences in 2/116 medulloblastomas, in 1/131 meningiomas, in 1/25 ependymomas and in 1/2 subependymomas. A single case of ependymoma contained SV40 VP-1 late gene sequences. Moreover, one of the meningioma samples showed JC virus sequences. In contrast, 60 hepatoblastoma samples and 31 brain samples from schizophrenic patients were consistently negative. BK virus sequences were not detectable in any of our samples. Immunohistochemical analysis of two SV40 positive tumor biopsies failed to detect large TAg in the tumor cells. In the JC positive meningioma, immunoreactivity for the viral late gene product (VP-1) was not observed. Our data do not entirely rule out SV40 and JC virus as an initiative agent with a hit-and-run mechanism. However the low frequency of virus sequences and the absence of TAg protein expression argue against a major role of these viruses in the pathogenesis of human medulloblastomas, meningiomas and ependymomas.

Indexed as

BK VirusBrain NeoplasmsCerebellar NeoplasmsEpendymomaHumansJC VirusMedulloblastomaMeningeal NeoplasmsMeningiomaPolymerase Chain ReactionSimian virus 40Tumor Cells, Cultured

Identifiers

PMID10668898
PMCPMC8098548
OpenAlexW2030615041

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.