Evidence map›Paper›PMID 22324795›Full record

ArticleBrain pathology (Zurich, Switzerland)2012

Analysis of chromosome 19q13.42 amplification in embryonal brain tumors with ependymoblastic multilayered rosettes.

Sumihito Nobusawa, Hideaki Yokoo, Junko Hirato, Akiyoshi Kakita, Hitoshi Takahashi, Takashi Sugino, Kazuhiro Tasaki, Hideaki Itoh, Tsutomu Hatori, Yoshie Shimoyama and 7 more

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
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  5. A surgical case of pediatric spinal medulloepithelioma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Medulloepithelioma with heterologous osteoid component: a case report and review of literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019
    Review
  10. Article
  11. Article
  12. Embryonal tumor with multilayered rosettes: illustrative case and review of the literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Review
  13. Review
  14. Review
  15. Review
  16. Article
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  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

17 authors at 10 institutions in 1 country.

Sumihito NobusawaDepartment of Human Pathology, Gunma University Graduate School of Medicine, Maebashi, Japan. nobusawa@showa.gunma-u.ac.jp
Hideaki Yokoo
Junko Hirato
Akiyoshi Kakita
Hitoshi Takahashi
Takashi Sugino
Kazuhiro Tasaki
Hideaki Itoh
Tsutomu Hatori
Yoshie Shimoyama
Atsuko Nakazawa
Shigeru Nishizawa
Hiroshi Kishimoto
Keiko Matsuoka
Masahiro Nakayama
Naoki Okura
Yoichi Nakazato
Gunma University · JPNiigata University · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPGunma University Hospital · JPNagoya University Hospital · JPNational Center For Child Health and Development · JPSaitama Children's Medical Center · JPThe University of Tokyo · JPToho University · JPUniversity of Occupational and Environmental Health Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, it was reported that ependymoblastoma and embryonal tumor with abundant neuropil and true rosettes (ETANTR) show 19q13.42 amplification at a high frequency, suggesting that these tumors may constitute a single entity. As ependymoblastic rosettes are the most prominent features in both subtypes, embryonal tumor with multilayered rosettes (ETMR) was proposed, for which 19q13.42 amplification represents a specific molecular hallmark. However, ependymoblastic rosettes are not specific to ependymoblastoma and ETANTR, and are also found in a few other embryonal tumors as well as immature teratomas, and knowledge on 19q13.42 amplification in these tumors is limited. In this study, we performed fluorescence in situ hybridazation (FISH) analysis and differential polymerase chain reaction (PCR), and detected 19q13.42 amplification in three out of four ETANTR, one ependymoblastoma and one medulloepithelioma with ETANTR components, whereas none of the two atypical teratoid/rhabdoid tumors (AT/RT) with ependymoblastic rosettes nor two immature teratomas with developing neuroectodermal structures showed such amplification, suggesting that medulloepitheliomas would possibly be included in ETMR, and ependymoblastic rosettes in AT/RT do not signify that these tumors constitute ETMR. Also, we found C19MC rather than miR-371-373 was amplified in one ETANTR, suggesting that C19MC miRNA cluster seems to be more closely linked to the pathogenesis of ETMR.

Indexed as

AdultBrain NeoplasmsChildChild, PreschoolChromosome DuplicationChromosomes, Human, Pair 19FemaleGene AmplificationHumansInfantInfant, NewbornMaleNeoplasms, Germ Cell and EmbryonalNeuroectodermal Tumors, PrimitiveNeuropilSynaptophysinSynaptophysin

Identifiers

PMID22324795
PMCPMC8057628
OpenAlexW1531005243

What OpenQuestion holds

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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.