How to treat histone 3 altered gliomas: molecular landscape and therapeutic developments

Vincenzo Di Nunno1, Enrico Franceschi2, Lidia Gatto1

  • 1Department of Oncology, AUSL Bologna, Bologna, Italy.

Abstract

Insights

Diffuse midline glioma (DMG) and diffuse hemispheric glioma (DHG) are rare brain tumors with distinct characteristics. Personalized therapy is crucial due to their divergent clinical and molecular behaviors, despite originating from the same gene.

Area of Science:

  • Neuro-oncology
  • Molecular Biology
  • Genetics

Background:

  • Diffuse midline glioma (DMG) and diffuse hemispheric glioma (DHG) are rare pediatric brain tumors.
  • Both are characterized by specific histone 3 alterations: H3K27 for DMG and H3G34 for DHG.
  • Despite a common genetic origin, DMG and DHG exhibit significant differences in clinical, radiological, and molecular profiles.

Conclusions:

  • DMG and DHG require distinct therapeutic strategies due to their unique biological and clinical characteristics.
  • Further research and clinical trials are needed to address the treatment gap for DHG.
  • Personalized medicine approaches are essential for optimizing outcomes in patients with these rare gliomas.