## Abstract Glioblastoma multiforme (GBM) is the most common and deadliest form of primary brain cancer in adults. Despite advances in molecular biology and genetics of cancer there is no currently available treatment for these tumors. Aberrant patterns of γ‐tubulin expression and compartmentalizat
Tubulin targets in the pathobiology and therapy of glioblastoma multiforme. I. class III β-tubulin
✍ Scribed by Christos D. Katsetos; Eduarda Dráberová; Agustin Legido; Charles Dumontet; Pavel Dráber
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 625 KB
- Volume
- 221
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
Glioblastoma multiforme (GBM) is the most common and deadliest form of primary brain cancer in adults. Despite advances in molecular biology and genetics of gliomas currently there is no effective treatment or promising molecularly targeted experimental therapeutic strategies for these tumors. In previous studies we have shown aberrant overexpression of the class III β‐tubulin isotype (βIII‐tubulin) in GBM and have proposed that this change may reflect perturbations in microtubule dynamics associated with glioma tumorigenesis, tumor progression and malignant transformation into GBM. This minireview focuses on microtubules and tubulin as emerging targets in potential therapy of GBM using a new class of βIII‐tubulin‐targeted drugs in the light of recent developments concerning the function and potential role of this isotype in clinically aggressive tumor behavior, cancer stem cells, tumor hypoxia and chemoresistance to tubulin binding agents, principally taxanes. J. Cell. Physiol. 221: 505–513, 2009. © 2009 Wiley‐Liss, Inc.
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