Evidence map›Paper›PMID 36505786›Full record

ArticleFrontiers in oncology2022

Epithelioid glioblastoma exhibits a heterogeneous molecular feature: A targeted next-generation sequencing study.

Rui Pan, Xiaotong Wang, Ru Fang, Qiuyuan Xia, Nan Wu, Qiu Rao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Rui PanDepartment of Pathology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Xiaotong WangDepartment of Pathology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Ru FangDepartment of Pathology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Qiuyuan XiaDepartment of Pathology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Nan WuDepartment of Pathology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Qiu RaoDepartment of Pathology, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Nanjing General Hospital of Nanjing Military Command · CNNanjing Medical University · CNNanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Epithelioid glioblastoma (eGBM) is one of the rare glioblastoma (GBM) variants in the current World Health Organization (WHO) categorization of central nervous system (CNS) tumours. However, the diagnostic basis and molecular features of eGBM have not been clearly defined to date. In this study, we aimed to molecularly characterize these tumours. Methods: The clinicopathological, molecular, and immunohistochemical characteristics of 12 cases of eGBM were investigated. Results: The tumours were found to be made up of epithelioid and rhabdoid cells when examined under a microscope. Six cases (50%) harboured the BRAF V600E mutation, and NF1 mutation was detected in 2 eGBM cases (16.7%). CDKN2A/B homozygous deletion was seen in 5 cases (41.7%). TP53 mutation was recognized in 2 instances (16.7%), and TERT promoter mutation was recognized in 5 cases (41.7%). Discussion: eGBM is characterized by high molecular heterogeneity and has molecular overlaps between low-grade gliomas. Moreover, rather than being a variant or entity, the biological significance of the "epithelioid" appearance may be reduced to a simply morphological pattern. In order to target the proper treatment to suitable patients, molecular stratification via genome-wide molecular profiling will be crucial.

Indexed as

BRAF V600Ecentral nervous system tumourepithelioid glioblastomaglioblastomamolecular genetics

Identifiers

PMID36505786
PMCPMC9730819
OpenAlexW4309915805

What OpenQuestion holds

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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.