Nguyen Anthony V, Soto Jose M, Gonzalez Sarah-Marie, Murillo Jennifer, Trumble Eric R, Shan Frank Y, Huang Jason H
Department of Neurosurgery, Baylor Scott and White Medical Center, Temple, TX 76508, USA.
Department of Neurology, Baylor Scott and White Medical Center, Temple, TX 76508, USA.
Biomedicines. 2023 Jul 15;11(7):2002. doi: 10.3390/biomedicines11072002.
The 2021 World Health Organization Classification of Tumors of the Central Nervous System reflected advances in understanding of the roles of oncohistones in gliomagenesis with the introduction of the H3.3-G34R/V mutant glioma to the already recognized H3-K27M altered glioma, which represent the diagnoses of pediatric-type diffuse hemispheric glioma and diffuse midline glioma, respectively. Despite advances in research regarding these disease entities, the prognosis remains poor. While many studies and clinical trials focus on H3-K27M-altered-glioma patients, those with H3.3-G34R/V mutant gliomas represent a particularly understudied population. Thus, we sought to review the current knowledge regarding the molecular mechanisms underpinning the gliomagenesis of H3.3-G34R/V mutant gliomas and the diagnosis, treatment, long-term outcomes, and possible future therapeutics.
《2021年世界卫生组织中枢神经系统肿瘤分类》反映了在对癌组蛋白在胶质瘤发生中的作用的理解方面取得的进展,其中将H3.3-G34R/V突变型胶质瘤纳入已被认可的H3-K27M改变的胶质瘤中,这两种胶质瘤分别代表儿童型弥漫性半球胶质瘤和弥漫性中线胶质瘤的诊断。尽管在关于这些疾病实体的研究方面取得了进展,但预后仍然很差。虽然许多研究和临床试验聚焦于H3-K27M改变的胶质瘤患者,但H3.3-G34R/V突变型胶质瘤患者是一个特别缺乏研究的群体。因此,我们试图综述目前关于H3.3-G34R/V突变型胶质瘤发生的分子机制以及诊断、治疗、长期预后和可能的未来治疗方法的知识。