Evidence map›Paper›PMID 30609203›Full record

ArticleCancer science2019

Genome-wide DNA methylation profiling shows molecular heterogeneity of anaplastic pleomorphic xanthoastrocytoma.

Taishi Nakamura, Kohei Fukuoka, Yoshiko Nakano, Kai Yamasaki, Yuko Matsushita, Satoshi Yamashita, Junji Ikeda, Naoko Udaka, Reo Tanoshima, Norio Shiba and 5 more

Abstract readCase Reports
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

15 authors.

Taishi NakamuraDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.ORCID http://orcid.org/0000-0003-1422-8957
Kohei FukuokaDivision of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.
Yoshiko NakanoDivision of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.
Kai YamasakiDivision of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.
Yuko MatsushitaDivision of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.
Satoshi YamashitaDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Junji IkedaDepartment of Pediatrics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Naoko UdakaDepartment of Pathology, Yokohama City University Hospital, Yokohama, Japan.
Reo TanoshimaDepartment of Pediatrics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Norio ShibaDepartment of Pediatrics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Kensuke TateishiDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Shoji YamanakaDepartment of Pathology, Yokohama City University Hospital, Yokohama, Japan.
Tetsuya YamamotoDepartment of Neurosurgery, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Junko HiratoDepartment of Pathology, Graduate School of Medicine, University Gunma, Maebashi, Japan.
Koichi IchimuraDivision of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.ORCID http://orcid.org/0000-0002-3851-2349

Funding

KAKENHI Grants-in-Aid for Scientific Research 18K16565 (T.N.)
6 · The paper itself

Abstract

In the revised World Health Organization classification 2016, anaplastic pleomorphic xanthoastrocytoma (PXA) has been newly defined as a variant of the PXA entity. Furthermore, some anaplastic PXA were reported to have extremely poor prognosis which showed a type of pediatric glioblastoma (GBM) molecular profile. Recent integrated molecular classification for primary central nervous system tumors proposed some differences between histological and molecular features. Herein, in a genome-wide molecular analysis, we show an extreme aggressive anaplastic PXA that resulted in a pediatric GBM molecular profile. A full implementation of the molecular approach is the key to predict prognosis and decide the treatment strategy for anaplastic PXA.

Indexed as

AdolescentAstrocytomaBrain NeoplasmsDNA MethylationFemaleGenome-Wide Association StudyGlioblastomaHumansPrognosisanaplastic PXAbrain tumorCpG islandDNA methylationpediatric glioblastoma

Identifiers

PMID30609203
PMCPMC6361572

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Registered trials

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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.