Prognostic Analysis of the IDH1 G105G (rs11554137) SNP in IDH-Wildtype Glioblastoma.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
12 08 2022
Historique:
received: 27 07 2022
revised: 10 08 2022
accepted: 11 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

The G105G SNP (rs11554137) in the IDH1 gene is observed in about 10-15% of patients with a diffuse glioma. Data regarding its impact on gliomas are poor and partially conflicting, possibly due to the evolving classification of CNS tumors. The aim of this study was to investigate the G105G SNP prognostic significance in a homogenous cohort of IDH-wildtype glioblastomas, in agreement with the 2021 WHO classification. The study analyzed 211 patients by collecting several clinico-pathological and molecular characteristics, including the age, lesion localization, number of involved lobes, type of surgical treatment, disease outcome and MGMT promoter methylation status. PFS and DSS curves were plotted according to the Kaplan-Meier method and statistical analyses were performed using parametric and non-parametric tests. A total of 32 patients out of 211 (15.2%) were found to be G105G SNP carriers. No significant impact of the IDH1 G105G SNP on patients' outcomes was observed in terms of PFS and DSS, while MGMT promoter methylation and gross total resection resulted as key prognostic factors in our cohort as expected. No prognostic impact of the IDH1 G105G SNP was detected in this strict cohort of IDH-wildtype glioblastomas. Analysis of larger cohorts is warranted to address the sample size limitations.

Identifiants

pubmed: 36011350
pii: genes13081439
doi: 10.3390/genes13081439
pmc: PMC9408597
pii:
doi:

Substances chimiques

Isocitrate Dehydrogenase EC 1.1.1.41
IDH1 protein, human EC 1.1.1.42.

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Ayoub Saaid (A)

Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Matteo Monticelli (M)

Neurosurgery Unit, Department of Neuroscience and Rehabilitation, University of Ferrara, 44100 Ferrara, Italy.

Alessia Andrea Ricci (AA)

Pathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.

Giulia Orlando (G)

Pathology Unit, Department of Oncology, University of Turin, 10126 Turin, Italy.

Cristina Botta (C)

Pathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.

Pietro Zeppa (P)

Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Andrea Bianconi (A)

Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Simona Osella-Abate (S)

Pathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.

Francesco Bruno (F)

Neuro-Oncology Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Alessia Pellerino (A)

Neuro-Oncology Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Roberta Rudà (R)

Neuro-Oncology Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.
Department of Neurology, Castelfranco and Treviso Hospitals, 31100 Treviso, Italy.

Paola Cassoni (P)

Pathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.

Diego Garbossa (D)

Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Fabio Cofano (F)

Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.

Luca Bertero (L)

Pathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.

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Classifications MeSH