Diffuse intrinsic pontine glioma: from diagnosis to next-generation clinical trials

NA Vitanza, M Monje - Current treatment options in neurology, 2019 - Springer
Purpose of review This review of diffuse intrinsic pontine glioma (DIPG) provides clinical
background, a systematic approach to diagnosis and initial care, and synthesizes historical …

Transcriptional dependencies in diffuse intrinsic pontine glioma

S Nagaraja, NA Vitanza, PJ Woo, KR Taylor, F Liu… - Cancer cell, 2017 - cell.com
Diffuse intrinsic pontine glioma (DIPG) is a fatal pediatric cancer with limited therapeutic
options. The majority of cases of DIPG exhibit a mutation in histone-3 (H3K27M) that results …

Recent advances in intradural spinal tumors

MM Abd-El-Barr, KT Huang, ZB Moses… - Neuro …, 2018 - academic.oup.com
Intradural spinal tumors are rare tumors of the central nervous system. Due to the eloquence
of the spinal cord and its tracts, the compact architecture of the cord and nerves, and the …

Non-inflammatory tumor microenvironment of diffuse intrinsic pontine glioma

GL Lin, S Nagaraja, MG Filbin, ML Suvà… - Acta neuropathologica …, 2018 - Springer
Diffuse intrinsic pontine glioma (DIPG) is a universally fatal malignancy of the childhood
central nervous system, with a median overall survival of 9–11 months. We have previously …

H3 K27M–mutant diffuse midline gliomas in different anatomical locations

L Wang, Z Li, M Zhang, Y Piao, L Chen, H Liang, Y Wei… - Human pathology, 2018 - Elsevier
Summary The histone H3 K27M mutation has been frequently reported in most diffuse
midline gliomas. However, the relationship between the H3 K27M mutation and clinical …

Progress in diffuse intrinsic pontine glioma: advocating for stereotactic biopsy in the standard of care

JR Williams, CC Young, NA Vitanza, M McGrath… - Neurosurgical …, 2020 - thejns.org
Diffuse intrinsic pontine glioma (DIPG) is a universally fatal pediatric brainstem tumor
affecting approximately 300 children in the US annually. Median survival is less than 1 year …

The molecular characteristics of spinal cord gliomas with or without H3 K27M mutation

RC Chai, YW Zhang, YQ Liu, YZ Chang, B Pang… - Acta Neuropathologica …, 2020 - Springer
Due to the rare incidence of spinal cord astrocytomas, their molecular features remain
unclear. Here, we characterized the landscapes of mutations in H3 K27M, isocitrate …

Surfaceome proteomic of glioblastoma revealed potential targets for immunotherapy

M Rose, T Cardon, S Aboulouard, N Hajjaji… - Frontiers in …, 2021 - frontiersin.org
Glioblastoma (GBM) is the most common and devastating malignant brain tumor in adults.
The mortality rate is very high despite different treatments. New therapeutic targets are …

Pediatric spinal pilocytic astrocytomas form a distinct epigenetic subclass from pilocytic astrocytomas of other locations and diffuse leptomeningeal glioneuronal …

A Métais, Y Bouchoucha, T Kergrohen… - Acta …, 2023 - Springer
Pediatric spinal low-grade glioma (LGG) and glioneuronal tumours are rare, accounting for
less 2.8–5.2% of pediatric LGG. New tumour types frequently found in spinal location such …

Genomic landscape of intramedullary spinal cord gliomas

M Zhang, RR Iyer, TD Azad, Q Wang… - Scientific reports, 2019 - nature.com
Intramedullary spinal cord tumors (IMSCTs) are rare neoplasms that have limited treatment
options and are associated with high rates of morbidity and mortality. To better understand …