DIPG-60. Avapritinib for targeting PDGFRA in H3K27M – mutated diffuse midline glioma [PDF]
Lisa Mayr +20 more
openalex +1 more source
Intravenous and intracranial GD2-CAR T cells for H3K27M+ diffuse midline gliomas
Abstract H3K27M-mutant diffuse midline gliomas (DMGs) express high levels of the disialoganglioside GD2 (ref. 1). Chimeric antigen receptor-modified T cells targeting GD2 (GD2-CART) eradicated DMGs in preclinical models1. Arm A of Phase I trial no. NCT04196413 (ref.
Michelle Monje +53 more
openaire +2 more sources
Rational combination platform trial design for children and young adults with diffuse midline glioma: A report from PNOC [PDF]
Background: Diffuse midline glioma (DMG) is a devastating pediatric brain tumor unresponsive to hundreds of clinical trials. Approximately 80% of DMGs harbor H3K27M oncohistones, which reprogram the epigenome to increase the metabolic profile of the ...
Franson, Andrea T +9 more
core +1 more source
EZHIP boosts neuronal-like synaptic gene programs and depresses polyamine metabolism
It is currently understood that the characteristic loss of the repressive histone mark H3K27me3 in PFA ependymoma and diffuse midline glioma (DMG) are caused by complementary mechanisms mediated by EZHIP and the oncohistone H3K27M, respectively.
Elham Hasheminasabgorji +12 more
doaj +1 more source
PATH-35. FREQUENCY AND CHARACTERISTICS OF H3K27M-MUTATION IN ADULTS WITH RADIOGRAPHICALLY-DETERMINED MIDLINE GLIOMAS [PDF]
Karisa C. Schreck +4 more
openalex +1 more source
FOXR2 Targets LHX6+/DLX+ Neural Lineages to Drive Central Nervous System Neuroblastoma [PDF]
Central nervous system neuroblastoma with forkhead box R2 (FOXR2) activation (NB-FOXR2) is a high-grade tumor of the brain hemispheres and a newly identified molecular entity.
Bandopadhayay, Pratiti +16 more
core +2 more sources
Characteristics of H3K27M-mutant diffuse gliomas with a non-midline location
Abstract Purpose: Diffuse midline gliomas (DMG) with H3K27 alterations (H3K27M-DMG) are a highly aggressive form of brain cancer. In rare cases, H3K27 mutations have been observed in diffuse non-midline gliomas (DNMG). It is currently unclear how these tumors should be classified.
Souhir, Guidara +14 more
openaire +2 more sources
An ERK5-PFKFB3 axis regulates glycolysis and represents a therapeutic vulnerability in pediatric diffuse midline glioma [PDF]
Metabolic reprogramming in pediatric diffuse midline glioma is driven by gene expression changes induced by the hallmark histone mutation H3K27M, which results in aberrantly permissive activation of oncogenic signaling pathways.
Agrawal, Nishant +32 more
core +1 more source
Elucidating intratumour heterogeneity through investigation of clonal, transcriptomic, and proteomic features across models of triple negative breast cancer and diffuse intrinsic pontine glioma [PDF]
Intratumour heterogeneity defines the diversity found within those malignant populations that take up residence within our bodies as cancer. These cellular societies comprise actors of diverse talents, from those suited to rapid proliferation, to drug ...
core +2 more sources
H2A.Z histone variants facilitate HDACi-dependent removal of H3.3K27M mutant protein in pediatric high-grade glioma cells [PDF]
Diffuse intrinsic pontine gliomas (DIPGs) are deadly pediatric brain tumors, non-resectable due to brainstem localization and diffusive growth.
et al., +3 more
core +2 more sources

