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High Incidence of MGMT and RARβ Promoter Methylation in Primary Glioblastomas: Association with Histopathological Characteristics, Inflammatory Mediators and Clinical Outcome

机译:MGMT和RARβ启动子甲基化在原发性胶质母细胞瘤中的高发病率:与组织病理学特征,炎症介质和临床结果的关联

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The successful treatment of glioblastoma multiforme (GBM), a life-threatening intracranial malignant tumor, is hindered by difficulties in early diagnosis, rapid progression and frequent recurrence. Since the methylation status of specific gene loci can be used as a prognostic tool for different tumor types, Piperi et al . examined four genes involved in glioma tumorigenesis: MGMT, RARβ, RASSF1A and CDH13 . The authors found that two of these genes, MGMT and RARβ were significantly more methylated in 70.58% and 58.8% of analysed GBM cases, respectively. This study also highlights a potential link between methylation patterns and IL-6, suggesting a specific role for inflammation mediators in the regulation of gene methylation. These results could generate new insight regarding patient survival and treatment options for this devastating disease.
机译:多形性胶质母细胞瘤(GBM)是一种威胁生命的颅内恶性肿瘤,但其成功治疗因早期诊断困难,进展迅速和复发频发而受到阻碍。由于特定基因位点的甲基化状态可以用作不同肿瘤类型的预后工具,Piperi等人。审查了涉及神经胶质瘤肿瘤发生的四个基因:MGMT,RARβ,RASSF1A和CDH13。作者发现,其中两个基因MGMT和RARβ分别在70.58%和58.8%的已分析GBM病例中甲基化程度更高。这项研究还强调了甲基化模式和IL-6之间的潜在联系,表明炎症介质在基因甲基化的调节中具有特殊作用。这些结果可能会为这种毁灭性疾病的患者生存和治疗选择带来新的见解。

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