Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective study

  • E. Miele
  • , E. Anghileri*
  • , C. Calatozzolo
  • , E. Lazzarini
  • , S. Patrizi
  • , A. Ciolfi
  • , L. Pedace
  • , M. Patane
  • , L. Abballe
  • , R. Paterra
  • , L. Maddaloni
  • , S. Barresi
  • , Angela Mastronuzzi
  • , A. Petruzzi
  • , I. Tramacere
  • , M. Farinotti
  • , L. Gurrieri
  • , E. Pirola
  • , M. Scarpelli
  • , G. Lombardi
  • V. Villani, M. Simonelli, R. Merli, A. Salmaggi, M. Tartaglia, A. Silvani, F. DiMeco, D. Calistri, E. Lamperti, Franco Locatelli, S. Indraccolo, B. Pollo
*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Five-year glioblastoma (GBM) survivors (LTS) are the minority of the isocitrate dehydrogenase (IDH)-wild-type GBM patients, and their molecular fingerprint is still largely unexplored. This multicenter retrospective study analyzed a large LTS-GBM cohort from nine Italian institutions and molecularly characterized a subgroup of patients by mutation, DNA methylation (DNAm) and copy number variation (CNV) profiling, comparing it to standard survival GBM. Mutation scan allowed the identification of pathogenic variants in most cases, showing a similar mutational spectrum in both groups, and highlighted TP53 as the most commonly mutated gene in the LTS group. We confirmed DNAm as a valuable tool for GBM classification with a diagnostic refinement by using brain tumor classifier v12.5. LTS were more heterogeneous with more cases classified as diffuse pediatric high-grade glioma subtypes and having peculiar CNVs. We observed a global higher methylation in CpG islands and in gene promoters of LTS with methylation levels of distinct gene promoters correlating with prognosis.
Lingua originaleInglese
pagine (da-a)1-10
Numero di pagine10
RivistaCancer Letters
Volume588
Numero di pubblicazione588
DOI
Stato di pubblicazionePubblicato - 2024

All Science Journal Classification (ASJC) codes

  • Oncologia
  • Ricerca sul Cancro

Keywords

  • Copy number variation
  • DNA methylation
  • IGFBP3
  • Long term survival glioblastoma
  • Mutation profile

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