Evidence map›Paper›PMID 35366170›Full record

ArticleCellular and molecular neurobiology2023

Clinical Prognostic Implications of Wnt Hub Genes Expression in Medulloblastoma.

Andrea Martins-da-Silva, Mirella Baroni, Karina Bezerra Salomão, Pablo Ferreira das Chagas, Ricardo Bonfim-Silva, Lenisa Geron, Gustavo Alencastro Veiga Cruzeiro, Wilson Araújo da Silva, Carolina Alves Pereira Corrêa, Carlos Gilberto Carlotti and 7 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2023. 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
0.3field-weighted citation impact, top 52% 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, 3 citations in OpenAlex.

  1. Article
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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

17 authors at 5 institutions in 2 countries.

Andrea Martins-da-Silva *Department of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil. amartinsdasilva@yahoo.com.br.ORCID http://orcid.org/0000-0002-1477-4360
Mirella Baroni *Department of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Karina Bezerra SalomãoDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Pablo Ferreira das ChagasDepartment of Genetics, Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Ricardo Bonfim-SilvaDepartment of Surgery and Anatomy, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Lenisa GeronDepartment of Genetics, Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Gustavo Alencastro Veiga CruzeiroDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Wilson Araújo da SilvaDepartment of Genetics, Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Carolina Alves Pereira CorrêaDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Carlos Gilberto CarlottiDepartment of Surgery and Anatomy, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Rosane Gomes de Paula QueirozDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Suely Kazue Nagahashi MarieDepartment of Neurology, São Paulo Medical School - University of São Paulo, São Paulo, Brazil.
Silvia Regina BrandaliseBoldrini Children's Center, Campinas, Brazil.
José Andrés YunesBoldrini Children's Center, Campinas, Brazil.
Carlos Alberto ScrideliDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Elvis Terci ValeraDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Luiz Gonzaga ToneDepartment of Pediatrics, University Hospital - Ribeirão Preto Medical School - University of São Paulo, Ribeirão Preto, Brazil.
Clinics Hospital of Ribeirão Preto · BRUniversidade de Ribeirão Preto · BRCentro Infantil Boldrini · BRDana-Farber Cancer Institute · USUniversidade de São Paulo · BR

Funding

coordenação de aperfeiçoamento de pessoal de nível superior 88882.317618/2019-01fundação de amparo à pesquisa do estado de são paulo 2014/20341-0
6 · The paper itself

Abstract

Medulloblastoma is the most common type of pediatric malignant primary brain tumor, and about one-third of patients die due to disease recurrence and most survivors suffer from long-term side effects. MB is clinically, genetically, and epigenetically heterogeneous and subdivided into at least four molecular subgroups: WNT, SHH, Group 3, and Group 4. We evaluated common differentially expressed genes between a Brazilian RNA-seq GSE181293 dataset and microarray GSE85217 dataset cohort of pediatric MB samples using bioinformatics methodology in order to identify hub genes of the molecular subgroups based on PPI network construction, survival and functional analysis. The main finding was the identification of five hub genes from the WNT subgroup that are tumor suppressors, and whose lower expression is related to a worse prognosis for MB patients. Furthermore, the common genes correlated with the five tumor suppressors participate in important pathways and processes for tumor initiation and progression, as well as development and differentiation, and some of them control cell stemness and pluripotency. These genes have not yet been studied within the context of MB, representing new important elements for investigation in the search for therapeutic targets, prognostic markers or for understanding of MB biology.

Indexed as

Brain NeoplasmsCerebellar NeoplasmsMedulloblastomaBiomarkers, TumorChildGene Expression ProfilingHumansPrognosisBiomarkers, TumorBioinformatics toolsBiomarkersHub genesMolecular SubgroupsTherapeutic targets

Identifiers

PMID35366170
PMCPMC11415171
OpenAlexW4226053374

What OpenQuestion holds

Textmetadata
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.