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Selective histone deacetylase inhibition as a therapeutically relevant strategy in H3K27M-glioma

delete2026-06-25
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OA
AI
A
Andrew Groves
O
Orville O Kirkland
C
Costanza Lo Cascio
X
Xiuqi Wang
C
Caleb Heaslip
J
Joana Graca Marques
C
Chen Song
R
Rebecca Poetschke
T
Tingjian Wang
D
Diana H Chin
Y
Yaw Asante
Q
Qi Liu
H
Hyunmin Kim
S
Shanqing Gu
M
Maria Trissal
J
Jenna Labelle
G
Gustavo Alencastro Veiga Cruzeiro
K
Kristen L Jones
A
Amy B Cameron
L
Louise M Clark
B
Brittaney Leeper
Q
Quang-De Nguyen
B
Berkley E Gryder
M
Mariella G Filbin *
J
Jun Qi *
DOI:10.1093/neuonc/noag142delete
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Abstract

Abstract

En 中文
Diffuse midline glioma (DMG) is a lethal pediatric brain tumor, driven by profound epigenetic dysregulation, raising the possibility that targeting epigenetic regulators such as histone deacetylases (HDACs) could provide a therapeutic benefit. However, despite preclinical activity, currently available HDAC inhibitors have shown limited clinical translation due to poor central nervous system (CNS) penetration and a lack of HDAC isoform selectivity.

Journal

N
Neuro-Oncology
IF:
13.4
Papers:
1.2W
Citations:
2.5W

Organization

H
harvard medical school
Scholars:
4.6K
Papers: 2.1K
Citations: 2
C
case western university school of medicine
Scholars:
6
Papers: 1
Citations: 0
D
dana-farber cancer institute
Scholars:
1.1K
Papers: 331
Citations: 0
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