| Literature DB >> 32348734 |
Madison Butler1, Lorinc Pongor2, Yu-Ting Su1, Liqiang Xi3, Mark Raffeld3, Martha Quezado3, Jane Trepel2, Kenneth Aldape3, Yves Pommier4, Jing Wu5.
Abstract
Glioblastoma is the most common primary malignant brain tumor. Although current standard therapy extends median survival to ~15 months, most patients do not have a sustained response to treatment. While O6-methylguanine (O6-MeG)-DNA methyltransferase (MGMT) promoter methylation status is accepted as a prognostic and promising predictive biomarker in glioblastoma, its value in informing treatment decisions for glioblastoma patients remains debatable. Discrepancies between MGMT promoter methylation status and treatment response in some patients may stem from inconsistencies between MGMT methylation and expression levels in glioblastoma. Here, we discuss MGMT as a biomarker and elucidate the discordance between MGMT methylation, expression, and patient outcome, which currently challenges the implementation of this biomarker in clinical practice. Published by Elsevier Inc.Entities:
Keywords: MGMT; biomarker; glioblastoma; neuro-oncology; precision medicine
Mesh:
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Year: 2020 PMID: 32348734 PMCID: PMC7315323 DOI: 10.1016/j.trecan.2020.02.010
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025