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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.
Introduction:
Diffuse midline gliomas (DMG) and diffuse hemispheric glioma (DHG) are both rare tumors characterized and recognized for specific alterations of histone 3 including H3K27 (DMG) and H3G34 (DHG). Despite these tumors arising from alterations of the same gene their clinical, radiological, and molecular behaviors strongly diverge, requiring a personalized therapeutic approach.
Areas Covered:
We performed a review on Medline/PudMed aiming to search papers relative to prospective trials, retrospective studies, case series, and case reports of interest in order to investigate current knowledge toward the main clinical and molecular characteristics, radiology, and diagnosis, loco-regional and systemic treatments of these tumors. Moreover, we also evaluated the novel treatments under investigation.
Expert Opinion:
Thanks to an increased knowledge of the genomic landscape of these rare tumors, there are novels promising therapeutic targets for these malignancies. However, the majority of available trials allowed enrollment only in DMG, while few studies are focused on or allow the inclusion of DHG patients.
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.
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