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HIN-1:一种对多形性胶质母细胞瘤治疗选择至关重要的新型表观遗传生物标志物。

HIN-1: a New Epigenetic Biomarker Crucial for Therapy Selection in Glioblastoma Multiforme.

作者信息

Herranz M, Padín-Iruegas M E, Martínez-Lago Nieves, Losada S Aguín, Raña-Díez P, Vázquez E Brozos, Carrera J J, Antúnez J R, Ruibal A, López-López R

机构信息

Nuclear Medicine Department, Molecular Imaging Program, IDIS, USC, Hospital Clínico Universitario. Fundación Tejerina, Santiago de Compostela, Spain.

Department of Functional Biology and Health Sciences, Human Anatomy and Embryology Section, University of Vigo, Vigo, Pontevedra, Spain.

出版信息

Mol Neurobiol. 2016 Apr;53(3):1802-1807. doi: 10.1007/s12035-015-9127-0. Epub 2015 Mar 11.

Abstract

Glioblastoma multiforme (GBM) is the most common brain tumor in adults. The role of high in normal-1 (HIN-1) as a potential biomarker in combating this disease is being described for the first time in this study. A combination of O6-methylguanine DNA methyltransferase (MGMT) and HIN-1 methylation could be a possible biomarker in therapy choice. Interestingly, survival data shows a similar trend for the methylation of MGMT and for unmethylation of HIN-1 and vice versa. Eighty-eight paraffin-embedded brain tumors were analyzed to screen methylation rates of different genes and evaluate the association between genes methylation and clinicopathologic variables. Our study is the first of its kind to indicate that MGMT and HIN-1 methylation status are inverted (97.7% of methylated ones) and could be new markers in the study of GBM prognosis, especially in the therapy selection.

摘要

多形性胶质母细胞瘤(GBM)是成人中最常见的脑肿瘤。本研究首次描述了正常高表达-1(HIN-1)作为对抗该疾病的潜在生物标志物的作用。O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)和HIN-1甲基化的组合可能是治疗选择中的一种生物标志物。有趣的是,生存数据显示MGMT甲基化和HIN-1未甲基化呈现相似趋势,反之亦然。对88例石蜡包埋的脑肿瘤进行分析,以筛选不同基因的甲基化率,并评估基因甲基化与临床病理变量之间的关联。我们的研究首次表明MGMT和HIN-1甲基化状态是相反的(97.7%为甲基化),并且可能是GBM预后研究中的新标志物,特别是在治疗选择方面。

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