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Cancer stem cell contribution to glioblastoma invasiveness

Glioblastoma (GBM) is the most aggressive and lethal brain tumor in adults. Its invasive nature currently represents the most challenging hurdle to surgical resection. The mechanism adopted by GBM cells to carry out their invasive strategy is an intricate program that recalls what takes place in emb...

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Autores principales: Ortensi, Barbara, Setti, Matteo, Osti, Daniela, Pelicci, Giuliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706754/
https://www.ncbi.nlm.nih.gov/pubmed/23510696
http://dx.doi.org/10.1186/scrt166
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author Ortensi, Barbara
Setti, Matteo
Osti, Daniela
Pelicci, Giuliana
author_facet Ortensi, Barbara
Setti, Matteo
Osti, Daniela
Pelicci, Giuliana
author_sort Ortensi, Barbara
collection PubMed
description Glioblastoma (GBM) is the most aggressive and lethal brain tumor in adults. Its invasive nature currently represents the most challenging hurdle to surgical resection. The mechanism adopted by GBM cells to carry out their invasive strategy is an intricate program that recalls what takes place in embryonic cells during development and in carcinoma cells during metastasis formation, the so-called epithelial-to-mesenchymal transition. GBM cells undergo a series of molecular and conformational changes shifting the tumor toward mesenchymal traits, including extracellular matrix remodeling, cytoskeletal re-patterning, and stem-like trait acquisition. A deeper understanding of the mechanisms driving the whole infiltrative process represents the first step toward successful treatment of this pathology. Here, we review recent findings demonstrating the invasive nature of GBM cancer stem cells, together with novel candidate molecules associated with both cancer stem cell biology and GBM invasion, like doublecortin and microRNAs. These findings may affect the design of effective therapies currently not considered for GBM invasive progression.
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spelling pubmed-37067542014-02-28 Cancer stem cell contribution to glioblastoma invasiveness Ortensi, Barbara Setti, Matteo Osti, Daniela Pelicci, Giuliana Stem Cell Res Ther Review Glioblastoma (GBM) is the most aggressive and lethal brain tumor in adults. Its invasive nature currently represents the most challenging hurdle to surgical resection. The mechanism adopted by GBM cells to carry out their invasive strategy is an intricate program that recalls what takes place in embryonic cells during development and in carcinoma cells during metastasis formation, the so-called epithelial-to-mesenchymal transition. GBM cells undergo a series of molecular and conformational changes shifting the tumor toward mesenchymal traits, including extracellular matrix remodeling, cytoskeletal re-patterning, and stem-like trait acquisition. A deeper understanding of the mechanisms driving the whole infiltrative process represents the first step toward successful treatment of this pathology. Here, we review recent findings demonstrating the invasive nature of GBM cancer stem cells, together with novel candidate molecules associated with both cancer stem cell biology and GBM invasion, like doublecortin and microRNAs. These findings may affect the design of effective therapies currently not considered for GBM invasive progression. BioMed Central 2013-02-28 /pmc/articles/PMC3706754/ /pubmed/23510696 http://dx.doi.org/10.1186/scrt166 Text en Copyright © 2013 BioMed Central Ltd
spellingShingle Review
Ortensi, Barbara
Setti, Matteo
Osti, Daniela
Pelicci, Giuliana
Cancer stem cell contribution to glioblastoma invasiveness
title Cancer stem cell contribution to glioblastoma invasiveness
title_full Cancer stem cell contribution to glioblastoma invasiveness
title_fullStr Cancer stem cell contribution to glioblastoma invasiveness
title_full_unstemmed Cancer stem cell contribution to glioblastoma invasiveness
title_short Cancer stem cell contribution to glioblastoma invasiveness
title_sort cancer stem cell contribution to glioblastoma invasiveness
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706754/
https://www.ncbi.nlm.nih.gov/pubmed/23510696
http://dx.doi.org/10.1186/scrt166
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