Department of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, Athens 11527, Greece; 1st Department of Neurosurgery, Evangelismos Hospital, National and Kapodistrian University of Athens, Greece.
Department of Medicine, Boston Medical Center, Boston University School of Medicine, Boston, MA 02118, USA.
Crit Rev Oncol Hematol. 2024 Dec;204:104532. doi: 10.1016/j.critrevonc.2024.104532. Epub 2024 Oct 13.
Glioma, an aggressive type of brain tumors of glial origin is highly heterogeneous, posing significant treatment challenges due to its intrinsic resistance to conventional therapeutic schemes. It is characterized by an interplay between epigenetic and genetic alterations in key signaling pathways which further endorse their resistance potential. Aberrant DNA methylation patterns, histone modifications and non-coding RNAs may alter the expression of genes associated with drug response and cell survival, induce gene silencing or deregulate key pathways contributing to glioma resistance. There is evidence that epigenetic plasticity enables glioma cells to adapt dynamically to therapeutic schemes and allow the formation of drug-resistant subpopulations. Furthermore, the tumor microenvironment adds an extra input on epigenetic regulation, increasing the complexity of resistance mechanisms. Herein, we discuss epigenetic changes conferring to drug resistance mechanisms in gliomas in order to delineate novel therapeutic targets and potential approaches that will enable personalized treatment.
神经胶质瘤是一种源自神经胶质的侵袭性脑肿瘤,具有高度异质性,由于其对常规治疗方案的固有耐药性,因此治疗极具挑战性。它的特征是关键信号通路中的表观遗传和遗传改变相互作用,进一步增强了其耐药潜力。异常的 DNA 甲基化模式、组蛋白修饰和非编码 RNA 可能改变与药物反应和细胞存活相关的基因表达,诱导基因沉默或使关键通路失调,从而导致神经胶质瘤耐药。有证据表明,表观遗传可塑性使神经胶质瘤细胞能够动态适应治疗方案,并允许形成耐药亚群。此外,肿瘤微环境增加了对表观遗传调控的额外输入,增加了耐药机制的复杂性。本文讨论了赋予神经胶质瘤耐药机制的表观遗传变化,以描绘新的治疗靶点和潜在的方法,从而实现个体化治疗。