Evidence map›Paper›PMID 34131151›Full record

ArticleNPJ genomic medicine2021

Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas.

Daisuke Ichikawa, Kyoko Yamashita, Yusuke Okuno, Hideki Muramatsu, Norihiro Murakami, Kyogo Suzuki, Daiei Kojima, Shinsuke Kataoka, Motoharu Hamada, Rieko Taniguchi and 13 more

Open access · goldAbstract read
In one paragraph

Article in NPJ genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Frontiers in oncology · 2025
    Article
  2. Article
  3. 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

23 authors at 7 institutions in 1 country.

Daisuke IchikawaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kyoko YamashitaDepartment of Pathology and Biological Responses, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yusuke OkunoMedical Genomics Center, Nagoya University Hospital, Nagoya, Japan.
Hideki MuramatsuDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-8801-0021
Norihiro MurakamiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kyogo SuzukiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Daiei KojimaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shinsuke KataokaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Motoharu HamadaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-2473-3730
Rieko TaniguchiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Eri NishikawaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nozomu KawashimaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0001-5700-4481
Atsushi NaritaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nobuhiro NishioDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Asahito HamaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kenji KasaiDepartment of Pathology, Aichi Medical University School of Medicine, Nagakute, Japan.
Seiji MizunoDepartment of Pediatrics, Central Hospital, Aichi Developmental Disability Center, Kasugai, Japan.
Yoshie ShimoyamaDepartment of Pathology and Laboratory Medicine, Nagoya University Hospital, Nagoya, Japan.
Masato NakaguroDepartment of Pathology and Laboratory Medicine, Nagoya University Hospital, Nagoya, Japan.
Hajime OkitaDepartment of Pathology, National Center for Child Health and Development, Tokyo, Japan.
Seiji KojimaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Atsuko NakazawaDepartment of Pathology, National Center for Child Health and Development, Tokyo, Japan.
Yoshiyuki TakahashiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan. ytakaha@med.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0001-8644-171X
Nagoya University · JPNagoya University Hospital · JPAichi Developmental Disability Center · JPAichi Medical University · JPKeio University · JPSaitama Children's Medical Center · JPThe Cancer Institute Hospital · JP

Funding

National Center for Child Health and Development (NCCHD) 26-20
6 · The paper itself

Abstract

Pediatric solid tumors are a heterogeneous group of neoplasms with over 100 subtypes. Clinical and histopathological diagnosis remains challenging due to the overlapping morphological and immunohistochemical findings and the presence of atypical cases. To evaluate the potential utility of including RNA-sequencing (RNA-seq) in the diagnostic process, we performed RNA-seq in 47 patients with suspected pediatric sarcomas. Histopathologists specialized in pediatric cancer re-evaluated pathological specimens to reach a consensus diagnosis; 42 patients were diagnosed with known subtypes of solid tumors whereas 5 patients were diagnosed with undifferentiated sarcoma. RNA-seq analysis confirmed and refined consensus diagnoses and further identified diagnostic genetic variants in four of the five patients with undifferentiated sarcoma. Genetic lesions were detected in 23 patients, including the novel SMARCA4-THOP1 fusion gene and 22 conventional or recently reported genetic events. Unsupervised clustering analysis of the RNA-seq data identified a distinct cluster defined by the overexpression of rhabdomyosarcoma-associated genes including MYOG and CHRNG. These findings suggest that RNA-seq-based genetic analysis may aid in the diagnosis of suspected pediatric sarcomas, which would be useful for the development of stratified treatment strategies.

Identifiers

PMID34131151
PMCPMC8206218
OpenAlexW3172603482

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.