Abe Hideaki, Natsumeda Manabu, Kanemaru Yu, Watanabe Jun, Tsukamoto Yoshihiro, Okada Masayasu, Yoshimura Junichi, Oishi Makoto, Fujii Yukihiko
Department of Neurosurgery, Brain Research Institute, Niigata University.
Neurol Med Chir (Tokyo). 2018 Jul 15;58(7):290-295. doi: 10.2176/nmc.ra.2018-0044. Epub 2018 May 31.
Histone H3 mutations are frequently found in diffuse midline gliomas (DMGs), which include diffuse intrinsic pontine gliomas and thalamic gliomas. These tumors have dismal prognoses. Recent evidence suggests that one reason for the poor prognoses is that O-methylguanine-DNA methyltransferase (MGMT) promoter frequently lacks methylation in DMGs. This review compares the epigenetic changes brought about by histone mutations to those by isocitrate dehydrogenase-mutant gliomas, which frequently have methylated MGMT promoters and are known to be sensitive to temozolomide.
组蛋白H3突变在弥漫性中线胶质瘤(DMG)中经常被发现,弥漫性中线胶质瘤包括弥漫性脑桥内胶质瘤和丘脑胶质瘤。这些肿瘤的预后很差。最近的证据表明,预后不良的一个原因是O-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子在弥漫性中线胶质瘤中经常缺乏甲基化。本综述比较了组蛋白突变与异柠檬酸脱氢酶突变型胶质瘤所带来的表观遗传变化,异柠檬酸脱氢酶突变型胶质瘤的MGMT启动子经常发生甲基化,并且已知对替莫唑胺敏感。