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Mechanisms of invasion and motility of high-grade gliomas in the brain.
Mair, Devin B; Ames, Heather M; Li, Rong.
Afiliación
  • Mair DB; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
  • Ames HM; Department of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201.
  • Li R; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Mol Biol Cell ; 29(21): 2509-2515, 2018 10 15.
Article en En | MEDLINE | ID: mdl-30325290
ABSTRACT
High-grade gliomas are especially difficult tumors to treat due to their invasive behavior. This has led to extensive research focusing on arresting glioma cell migration. Cell migration involves the sensing of a migratory cue, followed by polarization in the direction of the cue, and reorganization of the actin cytoskeleton to allow for a protrusive leading edge and a contractile trailing edge. Transmission of these forces to produce motility also requires adhesive interactions of the cell with the extracellular microenvironment. In glioma cells, transmembrane receptors such as CD44 and integrins bind the cell to the surrounding extracellular matrix that provides a substrate on which the cell can exert the requisite forces for cell motility. These various essential parts of the migratory machinery are potential targets to halt glioma cell invasion. In this review, we discuss the mechanisms of glioma cell migration and how they may be targeted in anti-invasion therapies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encéfalo / Movimiento Celular / Glioma Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Mol Biol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encéfalo / Movimiento Celular / Glioma Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Mol Biol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2018 Tipo del documento: Article
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