Evidence map›Paper›PMID 33924679›Full record

ArticleCancers2021

Reverse Engineering of Ewing Sarcoma Regulatory Network Uncovers PAX7 and RUNX3 as Master Regulators Associated with Good Prognosis.

Marcel da Câmara Ribeiro-Dantas, Danilo Oliveira Imparato, Matheus Gibeke Siqueira Dalmolin, Caroline Brunetto de Farias, André Tesainer Brunetto, Mariane da Cunha Jaeger, Rafael Roesler, Marialva Sinigaglia, Rodrigo Juliani Siqueira Dalmolin

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Does PAX7 and NKX2.2 immunoreactivity in Ewing sarcoma have prognostic significance?Virchows Archiv : an international journal of pathology · 2022
    Article
  8. The regulation of PBXs and their emerging role in cancer.Journal of cellular and molecular medicine · 2022
    Review
  9. Article
  10. 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

9 authors at 4 institutions in 2 countries.

Marcel da Câmara Ribeiro-DantasBioinformatics Multidisciplinary Environment-IMD, Federal University of Rio Grande do Norte, Natal 59078-400, Brazil.ORCID 0000-0001-5751-8386
Danilo Oliveira ImparatoBioinformatics Multidisciplinary Environment-IMD, Federal University of Rio Grande do Norte, Natal 59078-400, Brazil.ORCID 0000-0001-6979-4951
Matheus Gibeke Siqueira DalmolinChildren's Cancer Institute, Porto Alegre 90620-110, Brazil.ORCID 0000-0002-5400-0909
Caroline Brunetto de FariasChildren's Cancer Institute, Porto Alegre 90620-110, Brazil.ORCID 0000-0002-6435-6626
André Tesainer BrunettoChildren's Cancer Institute, Porto Alegre 90620-110, Brazil.ORCID 0000-0002-7958-1279
Mariane da Cunha JaegerChildren's Cancer Institute, Porto Alegre 90620-110, Brazil.ORCID 0000-0002-3465-4083
Rafael RoeslerCancer and Neurobiology Laboratory, Experimental Research Center, Clinical Hospital (CPE HCPA), Porto Alegre 90035-903, Brazil.ORCID 0000-0001-6016-2261
Marialva SinigagliaChildren's Cancer Institute, Porto Alegre 90620-110, Brazil.ORCID 0000-0002-8324-6860
Rodrigo Juliani Siqueira DalmolinBioinformatics Multidisciplinary Environment-IMD, Federal University of Rio Grande do Norte, Natal 59078-400, Brazil.ORCID 0000-0002-1688-6155
Hospital de Clínicas de Porto Alegre · BRUniversidade Federal do Rio Grande do Norte · BRUniversidade Federal do Rio Grande do Sul · BRUniversité Paris Sciences et Lettres · FR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 308258/2018-5Coordenação de Aperfeiçoamento de Pessoal de Nível Superior xxxxPronon 25000.202751/2016-65
6 · The paper itself

Abstract

Ewing Sarcoma (ES) is a rare malignant tumor occurring most frequently in adolescents and young adults. The ES hallmark is a chromosomal translocation between the chromosomes 11 and 22 that results in an aberrant transcription factor (TF) through the fusion of genes from the FET and ETS families, commonly EWSR1 and FLI1. The regulatory mechanisms behind the ES transcriptional alterations remain poorly understood. Here, we reconstruct the ES regulatory network using public available transcriptional data. Seven TFs were identified as potential MRs and clustered into two groups: one composed by PAX7 and RUNX3, and another composed by ARNT2, CREB3L1, GLI3, MEF2C, and PBX3. The MRs within each cluster act as reciprocal agonists regarding the regulation of shared genes, regulon activity, and implications in clinical outcome, while the clusters counteract each other. The regulons of all the seven MRs were differentially methylated. PAX7 and RUNX3 regulon activity were associated with good prognosis while ARNT2, CREB3L1, GLI3, and PBX3 were associated with bad prognosis. PAX7 and RUNX3 appear as highly expressed in ES biopsies and ES cell lines. This work contributes to the understanding of the ES regulome, identifying candidate MRs, analyzing their methilome and pointing to potential prognostic factors.

Indexed as

cancer of unknown primarypediatric cancerregulomesystems biologytranscription factor

Identifiers

PMID33924679
PMCPMC8070584
OpenAlexW3153478579

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.