Evidence map›Paper›PMID 39567898›Full record

ArticleBMC cancer2024

Classification of pediatric soft and bone sarcomas using DNA methylation-based profiling.

Felipe Luz Torres Silva, Mayara Ferreira Euzébio, Juliana Silveira Ruas, Mayra Troiani Franco, Alejandro Enzo Cassone, Thais Junqueira, Danielle Ribeiro Lucon, Izilda Aparecida Cardinalli, Luis Henrique Pereira, Priscila Pini Zenatti and 2 more

Abstract read
In one paragraph

Article in BMC cancer, 2024. 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
–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

4 citing papers in PubMed.

  1. Review
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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

12 authors.

Felipe Luz Torres SilvaResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil.
Mayara Ferreira EuzébioResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil.
Juliana Silveira RuasResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil.
Mayra Troiani FrancoBoldrini Children's Hospital, Campinas, São Paulo, Brazil.
Alejandro Enzo CassoneBoldrini Children's Hospital, Campinas, São Paulo, Brazil.
Thais JunqueiraBoldrini Children's Hospital, Campinas, São Paulo, Brazil.
Danielle Ribeiro LuconResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil.
Izilda Aparecida CardinalliBoldrini Children's Hospital, Campinas, São Paulo, Brazil.
Luis Henrique PereiraBoldrini Children's Hospital, Campinas, São Paulo, Brazil.
Priscila Pini ZenattiResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil.
Patricia Yoshioka JottaResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil.
Mariana MaschiettoResearch Center, Boldrini Children's Hospital, Rua Marcia Mendes, 619, Cidade Universitaria, CEP 13083-884, Campinas, São Paulo, Brazil. marianamasc@gmail.com.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 311141/2021-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/06782-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2022/04781-6PRONON SIPAR 25000.012259/2019-42PRONON SIPAR 25000.211368/2019-41
6 · The paper itself

Abstract

Pediatric sarcomas present heterogeneous morphology, genetics and clinical behavior posing a challenge for an accurate diagnosis. DNA methylation is an epigenetic modification that coordinates chromatin structure and regulates gene expression, determining cell type and function. DNA methylation-based tumor profiling classifier for sarcomas (known as sarcoma classifier) from the German Cancer Research Center (Deutsches Krebsforschungszentrum) was applied to 122 pediatric sarcomas referred to a reference pediatric oncology hospital. The classifiers reported 88.5% of agreement between histopathological and molecular classification confirming the initial diagnosis of all osteosarcomas and Ewing sarcomas. The Ewing-like sarcomas were reclassified into sarcomas with BCOR or CIC alterations, later confirmed by orthogonal diagnostic techniques. Regarding the CNAs profile, osteosarcomas had several chromosomal gains and losses as well as chromothripsis, whereas Ewing sarcomas had few large events, such as amplifications of chromosomes 8 and 12. The molecular classification together with clinical and histopathological assessment could improve the diagnosis of pediatric sarcomas although there are limitations to deal with more rare classes. This study provides an increase in the number of sarcomas evaluated for DNA methylation profiling in the pediatric population.

Indexed as

Bone NeoplasmsDNA MethylationOsteosarcomaSarcoma, EwingAdolescentChildChild, PreschoolDNA Copy Number VariationsFemaleGene Expression ProfilingHumansInfantMaleSarcomaSoft Tissue NeoplasmsCopy number alterationDNA methylationMolecular classificationPediatric sarcomasSoft and bone sarcomas

Identifiers

PMID39567898
PMCPMC11577672

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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.