Evidence map›Paper›PMID 25268364›Full record

ArticlePloS one2014

Human cytomegalovirus tegument protein pp65 is detected in all intra- and extra-axial brain tumours independent of the tumour type or grade.

Sylwia Libard, Svetlana N Popova, Rose-Marie Amini, Vesa Kärjä, Timo Pietiläinen, Kirsi M Hämäläinen, Christer Sundström, Göran Hesselager, Michael Bergqvist, Simon Ekman and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Once, Twice, Three Times a Finding: Reproducibility of Dendritic Cell Vaccine Trials Targeting Cytomegalovirus in Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Trial
  3. Article
  4. Does human cytomegalovirus provide a novel therapeutic target for patients with glioblastoma?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  5. Review
  6. Review
  7. Mechanistic insights into medulloblastoma relapse.Pharmacology & therapeutics · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Uncovering tau in wasteosomes (Frontiers in aging neuroscience · 2023
    Article
  12. Wasteosomes (Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Human Cytomegalovirus DNA among Women with Breast Cancer.Asian Pacific journal of cancer prevention : APJCP · 2019
    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

18 authors at 5 institutions in 2 countries.

Sylwia LibardDepartment of Pathology, Uppsala University Hospital, Uppsala, Sweden; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Svetlana N PopovaDepartment of Pathology, Uppsala University Hospital, Uppsala, Sweden; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Rose-Marie AminiDepartment of Pathology, Uppsala University Hospital, Uppsala, Sweden; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Vesa KärjäDepartment of Clinical Pathology, Kuopio University Hospital, Kuopio, Finland.
Timo PietiläinenDepartment of Clinical Pathology, Kuopio University Hospital, Kuopio, Finland.
Kirsi M HämäläinenDepartment of Clinical Pathology, Kuopio University Hospital, Kuopio, Finland.
Christer SundströmDepartment of Pathology, Uppsala University Hospital, Uppsala, Sweden; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Göran HesselagerDepartment of Neurosurgery, Uppsala University Hospital, Uppsala, Sweden.
Michael BergqvistDepartment of Oncology, Centre for Research & Development, County Council of Gävleborg, Gävle Hospital, Gävle, Sweden; Department of radiation sciences, Umeå University, Umeå, Sweden.
Simon EkmanDepartment of Radiology, Oncology and Radiation Science, Section of Oncology, Uppsala University, Uppsala, Sweden.
Maria ZetterlingDepartment of Neurosurgery, Uppsala University Hospital, Uppsala, Sweden.
Anja SmitsDepartment of Neuroscience Neurology, Uppsala University, Uppsala, Sweden.
Pelle NilssonDepartment of Neurosurgery, Uppsala University Hospital, Uppsala, Sweden.
Susan PfeiferDepartment of Women's and Children's Health, Uppsala University, Uppsala University Hospital, Uppsala, Sweden.
Teresita Diaz de StåhlDepartment of Oncology-Pathology, Karolinska Institutet, Cancer Center Karolinska, Karolinska University Hospital, Stockholm, Sweden.
Gunilla EnbladDepartment of Radiology, Oncology and Radiation Science, Section of Oncology, Uppsala University, Uppsala, Sweden.
Fredrik PontenDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Irina AlafuzoffDepartment of Pathology, Uppsala University Hospital, Uppsala, Sweden; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Uppsala University · SEUppsala University Hospital · SEKuopio University Hospital · FIKarolinska University Hospital · SEUmeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) has been indicated being a significant oncomodulator. Recent reports have suggested that an antiviral treatment alters the outcome of a glioblastoma. We analysed the performance of commercial HCMV-antibodies applying the immunohistochemical (IHC) methods on brain sample obtained from a subject with a verified HCMV infection, on samples obtained from 14 control subjects, and on a tissue microarray block containing cores of various brain tumours. Based on these trials, we selected the best performing antibody and analysed a cohort of 417 extra- and intra-axial brain tumours such as gliomas, medulloblastomas, primary diffuse large B-cell lymphomas, and meningiomas. HCMV protein pp65 immunoreactivity was observed in all types of tumours analysed, and the IHC expression did not depend on the patient's age, gender, tumour type, or grade. The labelling pattern observed in the tumours differed from the labelling pattern observed in the tissue with an active HCMV infection. The HCMV protein was expressed in up to 90% of all the tumours investigated. Our results are in accordance with previous reports regarding the HCMV protein expression in glioblastomas and medulloblastomas. In addition, the HCMV protein expression was seen in primary brain lymphomas, low-grade gliomas, and in meningiomas. Our results indicate that the HCMV protein pp65 expression is common in intra- and extra-axial brain tumours. Thus, the assessment of the HCMV expression in tumours of various origins and pathologically altered tissue in conditions such as inflammation, infection, and even degeneration should certainly be facilitated.

Indexed as

AdolescentAdultAgedAged, 80 and overBrain NeoplasmsCohort StudiesCytomegalovirusFemaleGlioblastomaHumansImmunohistochemistryLymphomaMaleMedulloblastomaMeningiomaMiddle Agedcytomegalovirus matrix protein 65kDaPhosphoproteinsViral Matrix Proteins

Identifiers

PMID25268364
PMCPMC4182568
OpenAlexW2000647838

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.