| Literature DB >> 26614346 |
Amanda Thomaz1,2, Mariane Jaeger1,2, Marienela Buendia1,2, Victorio Bambini-Junior3, Lauro José Gregianin1,4, Algemir Lunardi Brunetto1,5, André T Brunetto1,5, Caroline Brunetto de Farias1,5, Rafael Roesler6,7,8.
Abstract
Medulloblastoma (MB) is the most common malignant pediatric brain tumor. Deregulation of brain-derived neurotrophic factor (BDNF)/tropomyosin-related kinase B (TrkB) signaling has been associated with increased proliferative capabilities, invasiveness, and chemoresistance in several types of cancer. However, the relevance of this pathway in MB remains unknown. Here, we show that the selective TrkB inhibitor N-[2-[[(hexahydro-2-oxo-1H-azepin-3-yl)amino]carbonyl]phenyl]-benzo[b]thiophene-2-carboxamide (ANA-12) markedly reduced the viability and survival of human cell lines representative of different MB molecular subgroups. These findings provide the first evidence supporting further investigation of TrkB inhibition as a potential novel strategy for MB treatment.Entities:
Keywords: Brain tumor; Brain-derived neurotrophic factor; Childhood cancer; Medulloblastoma; TrkB
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Year: 2015 PMID: 26614346 DOI: 10.1007/s12031-015-0689-0
Source DB: PubMed Journal: J Mol Neurosci ISSN: 0895-8696 Impact factor: 3.444