Evidence map›Paper›PMID 15655550›Full record

ArticleBritish journal of cancer2005

Survivin, Survivin-2B, and Survivin-deItaEx3 expression in medulloblastoma: biologic markers of tumour morphology and clinical outcome.

J R Fangusaro, Y Jiang, M P Holloway, H Caldas, V Singh, D R Boué, J Hayes, R A Altura

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01556178 (Collection of Blood and Cerebrospinal Fluid for Pediatric Brain Tumor Research), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.2field-weighted citation impact, top 5% 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.

NCT01556178 completednot on this mapstarted 2011, after this paper: background citation

Collection of Blood and Cerebrospinal Fluid for Pediatric Brain Tumor Research

TypeobservationalSponsorAnn & Robert H Lurie Children's Hospital of ChicagoRan2011 to 2012Enrolled5ConditionsHydrocephalus
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. CD44 mediates stem cell mobilization to damaged lungInternational journal of medical sciences · 2020
    Article
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  11. Review
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  17. Survivin gene-expression and splicing isoforms in oral squamous cell carcinoma.Journal of cancer research and clinical oncology · 2009
    Article
  18. Review
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

J R FangusaroCenter for Childhood Cancer Research, Columbus Children's Research Institute (CCRI), College of Medicine and Public Health, The Ohio State University, 700 Children's Drive, Columbus, OH 43205, USA.
Y Jiang
M P Holloway
H Caldas
V Singh
D R Boué
J Hayes
R A Altura
The Ohio State University · USCommunity College of Rhode Island · USNationwide Children's Hospital · US

Funding

NICHD Institutional Training for Pediatricians (T32)T32HD043003 · NICHD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BARNARD, JOHN A · 2003 to 2014
$1.7M
NICHD NIH HHS T32 HD043003NICHD NIH HHS T32 HD043003-02
6 · The paper itself

Abstract

Survivin is an apoptotic inhibitor that is expressed at high levels in a variety of malignancies. Survivin has four known alternative splice forms (Survivin, Survivin-2B, Survivin-deltaEx3, and Survivin-3B), and the recent literature suggests that these splice variants have unique functions and subcellular localisation patterns. We evaluated 19 fresh-frozen paediatric medulloblastomas for the expression of three Survivin isoforms by quantitative PCR. Survivin was most highly expressed when compared with normal cerebellar tissue. We also investigated Survivin protein expression in 40 paraffin-embedded paediatric medulloblastoma tumours by immunohistochemistry. We found a statistically significant association between the percentage of Survivin-positive cells and histologic subtype, with the large-cell-anaplastic variant expressing Survivin at higher levels than the classic subtype. We also found a statistically significant relationship between the percent of Survivin-positive cells in the tumours and clinical outcome, with higher levels of Survivin correlating with a worse prognosis. In summary, our study demonstrates a role for Survivin as a marker of tumour morphology and clinical outcome in medulloblastoma. Survivin may be a promising future prognostic tool and potential biologic target in this malignancy.

Indexed as

Biomarkers, TumorBlotting, WesternCerebellar NeoplasmsChildFemaleHumansImmunohistochemistryInhibitor of Apoptosis ProteinsMaleMedulloblastomaMicrotubule-Associated ProteinsNeoplasm ProteinsPolymerase Chain ReactionPrognosisProtein IsoformsRecombination, GeneticBiomarkers, TumorBIRC5 protein, humanInhibitor of Apoptosis ProteinsMicrotubule-Associated ProteinsNeoplasm ProteinsProtein IsoformsSurvivin

Identifiers

PMID15655550
PMCPMC2361849
OpenAlexW1997062019

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.