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Advances in HSP27 and HSP90-targeting strategies for glioblastoma.
van Ommeren, Randy; Staudt, Michael D; Xu, Hu; Hebb, Matthew O.
Afiliação
  • van Ommeren R; Department of Clinical Neurological Sciences, Western University, 339 Windermere Road, Suite C7-134, London, ON, N6A 5A5, Canada.
  • Staudt MD; Department of Clinical Neurological Sciences, Western University, 339 Windermere Road, Suite C7-134, London, ON, N6A 5A5, Canada.
  • Xu H; Department of Clinical Neurological Sciences, Western University, 339 Windermere Road, Suite C7-134, London, ON, N6A 5A5, Canada.
  • Hebb MO; Department of Clinical Neurological Sciences, Western University, 339 Windermere Road, Suite C7-134, London, ON, N6A 5A5, Canada. mhebb@uwo.ca.
J Neurooncol ; 127(2): 209-19, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26842818
ABSTRACT
Glioblastoma (GBM) is the most common and malignant primary brain tumor in adults. There is a critical need for novel strategies to abolish the molecular mechanisms that support GBM growth, invasion and treatment resistance. The heat shock proteins, HSP27 and HSP90, serve these pivotal roles in tumor cells and have been identified as effective targets for developing therapeutics. Natural and synthetic inhibitors have been evaluated in clinical trials for several forms of systemic cancer but none as yet for GBM. This topic review summarizes the current preclinical evidence and rationale to define the potential of HSP27 and HSP90 inhibitors in GBM management.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glioblastoma / Proteínas de Choque Térmico HSP90 / Proteínas de Choque Térmico HSP27 / Terapia de Alvo Molecular / Antineoplásicos Limite: Adult / Humans Idioma: En Revista: J Neurooncol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glioblastoma / Proteínas de Choque Térmico HSP90 / Proteínas de Choque Térmico HSP27 / Terapia de Alvo Molecular / Antineoplásicos Limite: Adult / Humans Idioma: En Revista: J Neurooncol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá