Epigenetic alterations in glioblastomas: Diagnostic, prognostic and therapeutic relevance

被引:14
|
作者
Montella, Liliana [1 ]
Cuomo, Mariella [2 ,3 ]
Del Gaudio, Nunzio [4 ]
Buonaiuto, Michela [2 ,3 ]
Costabile, Davide [2 ,5 ]
Visconti, Roberta [2 ,6 ]
Di Risi, Teodolinda [2 ,7 ]
Vinciguerra, Roberta [2 ]
Trio, Federica [2 ]
Ferraro, Sara [2 ]
Bove, Guglielmo [4 ]
Facchini, Gaetano [1 ]
Altucci, Lucia [4 ,8 ,9 ]
Chiariotti, Lorenzo [2 ,3 ,10 ]
Della Monica, Rosa [2 ,3 ]
机构
[1] Santa Maria Grazie Hosp, Oncol Operat Unit, ASL NA2 NORD, Pozzuoli, Italy
[2] CEINGE Biotecnol Avanzate scarl, Naples, Italy
[3] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, Naples, Italy
[4] Univ Campania Luigi Vanvitelli, Dept Precis Med, Naples, Italy
[5] Univ Naples Federico II, European Sch Mol Med, SEMM, Naples, Italy
[6] Italian Natl Council Res, Inst Expt Endocrinol & Oncol, Naples, Italy
[7] Univ Naples Federico II, Dept Publ Hlth, Naples, Italy
[8] BIOGEM, Ariano Irpino, Italy
[9] Univ Campania Luigi Vanvitelli, Dept Precis Med, Vico L Crecchio 7, I-80138 Naples, Italy
[10] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, via S Pansini 5, I-80131 Naples, Italy
关键词
DNA methylation; glioblastoma; histone modifications; molecular classification; targeted therapy; CENTRAL-NERVOUS-SYSTEM; CELL-PROLIFERATION; GENE METHYLATION; SELF-RENEWAL; MGMT; INHIBITION; CLASSIFICATION; TEMOZOLOMIDE; EXPRESSION; GROWTH;
D O I
10.1002/ijc.34381
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma, the most common and heterogeneous tumor affecting brain parenchyma, is dismally characterized by a very poor prognosis. Thus, the search of new, more effective treatments is a vital need. Here, we will review the druggable epigenetic features of glioblastomas that are, indeed, currently explored in preclinical studies and in clinical trials for the development of more effective, personalized treatments. In detail, we will review the studies that have led to the identification of epigenetic signatures, IDH mutations, MGMT gene methylation, histone modification alterations, H3K27 mutations and epitranscriptome landscapes of glioblastomas, in each case discussing the corresponding targeted therapies and their potential efficacy. Finally, we will emphasize how recent technological improvements permit to routinely investigate many glioblastoma epigenetic biomarkers in clinical practice, further enforcing the hope that personalized drugs, targeting specific epigenetic features, could be in future a therapeutic option for selected patients.
引用
收藏
页码:476 / 488
页数:13
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