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Galectins and Gliomas
Malignant gliomas, especially glioblastomas, are associated with a dismal prognosis. Despite advances in diagnosis and treatment, glioblastoma patients still have a median survival expectancy of only 14 months. This poor prognosis can be at least partly explained by the fact that glioma cells diffus...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805916/ https://www.ncbi.nlm.nih.gov/pubmed/19371355 http://dx.doi.org/10.1111/j.1750-3639.2009.00270.x |
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author | Le Mercier, Marie Fortin, Shannon Mathieu, Véronique Kiss, Robert Lefranc, Florence |
author_facet | Le Mercier, Marie Fortin, Shannon Mathieu, Véronique Kiss, Robert Lefranc, Florence |
author_sort | Le Mercier, Marie |
collection | PubMed |
description | Malignant gliomas, especially glioblastomas, are associated with a dismal prognosis. Despite advances in diagnosis and treatment, glioblastoma patients still have a median survival expectancy of only 14 months. This poor prognosis can be at least partly explained by the fact that glioma cells diffusely infiltrate the brain parenchyma and exhibit decreased levels of apoptosis, and thus resistance to cytotoxic drugs. Galectins are a family of mammalian beta‐galactoside‐binding proteins characterized by a shared characteristic amino acid sequence. They are expressed differentially in normal vs. neoplastic tissues and are known to play important roles in several biological processes such as cell proliferation, death and migration. This review focuses on the role played by galectins, especially galectin‐1 and galectin‐3, in glioma biology. The involvement of these galectins in different steps of glioma malignant progression such as migration, angiogenesis or chemoresistance makes them potentially good targets for the development of new drugs to combat these malignant tumors. |
format | Text |
id | pubmed-2805916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-28059162010-01-21 Galectins and Gliomas Le Mercier, Marie Fortin, Shannon Mathieu, Véronique Kiss, Robert Lefranc, Florence Brain Pathol Review Articles Malignant gliomas, especially glioblastomas, are associated with a dismal prognosis. Despite advances in diagnosis and treatment, glioblastoma patients still have a median survival expectancy of only 14 months. This poor prognosis can be at least partly explained by the fact that glioma cells diffusely infiltrate the brain parenchyma and exhibit decreased levels of apoptosis, and thus resistance to cytotoxic drugs. Galectins are a family of mammalian beta‐galactoside‐binding proteins characterized by a shared characteristic amino acid sequence. They are expressed differentially in normal vs. neoplastic tissues and are known to play important roles in several biological processes such as cell proliferation, death and migration. This review focuses on the role played by galectins, especially galectin‐1 and galectin‐3, in glioma biology. The involvement of these galectins in different steps of glioma malignant progression such as migration, angiogenesis or chemoresistance makes them potentially good targets for the development of new drugs to combat these malignant tumors. Blackwell Publishing Ltd 2009-04-09 /pmc/articles/PMC2805916/ /pubmed/19371355 http://dx.doi.org/10.1111/j.1750-3639.2009.00270.x Text en © 2009 The Authors. Journal Compilation © 2009 International Society of Neuropathology Open access. |
spellingShingle | Review Articles Le Mercier, Marie Fortin, Shannon Mathieu, Véronique Kiss, Robert Lefranc, Florence Galectins and Gliomas |
title | Galectins and Gliomas |
title_full | Galectins and Gliomas |
title_fullStr | Galectins and Gliomas |
title_full_unstemmed | Galectins and Gliomas |
title_short | Galectins and Gliomas |
title_sort | galectins and gliomas |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805916/ https://www.ncbi.nlm.nih.gov/pubmed/19371355 http://dx.doi.org/10.1111/j.1750-3639.2009.00270.x |
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