Targeting epigenetic mechanisms of resistance to chemotherapy in gliomas

被引:2
|
作者
Skouras, Panagiotis [1 ,2 ]
Markouli, Mariam [3 ]
Papadatou, Ioanna [4 ]
Piperi, Christina [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Med Sch, Dept Biol Chem, 75 Mikras Asias St Bldg 16, Athens 11527, Greece
[2] Natl & Kapodistrian Univ Athens, Evangelismos Hosp, Dept Neurosurg 1, Athens 11527, Greece
[3] Boston Univ, Sch Med, Boston Med Ctr, Dept Med, Boston, MA 02118 USA
[4] Natl & Kapodistrian Univ Athens, Univ Res Inst Study Genet & Malignant Disorders Ch, Aghia Sophia Childrens Hosp, Athens 11527, Greece
关键词
Gliomas; Drug resistance; Histone deacetylases; TMZ; HDAC inhibitors; Lysine demethylases; MiRNAs; LncRNAs; O-6-METHYLGUANINE DNA METHYLTRANSFERASE; ENDOPLASMIC-RETICULUM STRESS; HUMAN GLIOBLASTOMA CELLS; CENTRAL-NERVOUS-SYSTEM; TEMOZOLOMIDE RESISTANCE; RECURRENT GLIOBLASTOMA; STEM-CELLS; PHASE-II; IN-VITRO; INHIBITION;
D O I
10.1016/j.critrevonc.2024.104532
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页数:11
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