| Literature DB >> 25752997 |
M Herranz1, M E Padín-Iruegas2, Nieves Martínez-Lago3, S Aguín Losada3, P Raña-Díez3, E Brozos Vázquez3, J J Carrera4, J R Antúnez4, A Ruibal5, R López-López3.
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.Entities:
Keywords: Epigenetics; Glioblastoma; HIN1; Outcome; Therapy
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Year: 2015 PMID: 25752997 DOI: 10.1007/s12035-015-9127-0
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590