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ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Opposite patterns of association of TWIST1 expression with patient survival in SHH and Group 4 medulloblastoma.

Karina Munhoz de Paula Alves Coelho, Matheus Dalmolin, Francis Rossetti Pedack, José Guilherme Pickler, Camila Barbosa, Julio Recalde, Rodrigo Blasius, Bruna Louise Silva, Marcelo A C Fernandes, Hercilio Fronza Junior and 2 more

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Karina Munhoz de Paula Alves CoelhoDepartment of Scientific Development and Innovation (DECIPE), Center for Anatomo-Pathological Diagnosis (CEDAP), Joinville, Brazil. karina@cedap.com.br.
Matheus DalmolinNational Science and Technology Institute for Children's Cancer Biology and Pediatric Oncology-INCT BioOncoPed, Porto Alegre, Brazil.
Francis Rossetti PedackGraduate Program in Health and Environmental Sciences, University of Joinville (UNIVILLE), Joinville, Brazil.
José Guilherme PicklerGraduate Program in Health and Environmental Sciences, University of Joinville (UNIVILLE), Joinville, Brazil.
Camila BarbosaDepartment of Scientific Development and Innovation (DECIPE), Center for Anatomo-Pathological Diagnosis (CEDAP), Joinville, Brazil.
Julio RecaldeDepartment of Scientific Development and Innovation (DECIPE), Center for Anatomo-Pathological Diagnosis (CEDAP), Joinville, Brazil.
Rodrigo BlasiusDepartment of Scientific Development and Innovation (DECIPE), Center for Anatomo-Pathological Diagnosis (CEDAP), Joinville, Brazil.
Bruna Louise SilvaDepartment of Scientific Development and Innovation (DECIPE), Center for Anatomo-Pathological Diagnosis (CEDAP), Joinville, Brazil.
Marcelo A C FernandesNational Science and Technology Institute for Children's Cancer Biology and Pediatric Oncology-INCT BioOncoPed, Porto Alegre, Brazil.
Hercilio Fronza JuniorDepartment of Scientific Development and Innovation (DECIPE), Center for Anatomo-Pathological Diagnosis (CEDAP), Joinville, Brazil.
Paulo Henrique Condeixa de FrançaGraduate Program in Health and Environmental Sciences, University of Joinville (UNIVILLE), Joinville, Brazil.
Rafael RoeslerNational Science and Technology Institute for Children's Cancer Biology and Pediatric Oncology-INCT BioOncoPed, Porto Alegre, Brazil. rafaelroesler@hcpa.edu.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 305647/2019-9Conselho Nacional de Desenvolvimento Científico e Tecnológico 406484/2022-8
6 · The paper itself

Abstract

purposeTwist1 is a transcription factor that regulates embryonic development, stemness, and differentiation, and can also stimulate initiation of tumorigenesis in peripheral solid cancers. However, its role in central nervous system tumors, including medulloblastoma (MB), the main type of malignant brain cancer that afflicts children, remains poorly understood. Here, we examined expression of Twist1, and its potential significance in prognosis, in different histological variants and molecular subgroups of MB.

methodsGene expression data for TWIST1 and corresponding overall survival (OS) of patients was analyzed in 612 MB samples using a previously described dataset. A cross-sectional analysis of Twist1 protein content in 24 MB tumor samples from patients was carried out by immunohistochemistry.

resultsTWIST1 transcript levels were higher in classic MB compared to desmoplastic tumors. Within samples with classic histology, higher TWIST1 expression was associated with a longer OS. Tumors in the SHH subgroup had lower TWIST1 expression compared to all other subgroups, and Group 4 showed lower expression than WNT tumors. In Group 4 MB, higher TWIST1 levels were associated with shorter OS, whereas patients with SHH tumors and higher TWIST1 levels showed longer OS. Twist1 protein was detectable in part of classic and LCA MB tumors belonging to the SHH, WNT, or Group 3/4 subgroups.

conclusionWe found opposite patterns of association between TWST1 and patient survival in Group 4 and SHH MB subgroups. Our results highlight the importance of stratifying tumors by molecular subgroup and histological classification when exploring novel potential biomarkers and therapeutic targets in MB.

Indexed as

Cerebellar NeoplasmsHedgehog ProteinsMedulloblastomaNuclear ProteinsTwist-Related Protein 1AdolescentChildChild, PreschoolCross-Sectional StudiesFemaleGene Expression Regulation, NeoplasticHumansInfantMalePrognosisHedgehog ProteinsNuclear ProteinsSHH protein, humanTWIST1 protein, humanTwist-Related Protein 1Brain tumorMedulloblastomaTranscription factorTwist1

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