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Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma
Glioblastoma (GBM) is the most commonly diagnosed malignant brain tumor in adults. The prognosis for patients with GBM remains poor and largely unchanged over the last 30 years, due to the limitations of existing therapies. Thus, new therapeutic approaches are desperately required. Sphingolipids are...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017054/ https://www.ncbi.nlm.nih.gov/pubmed/31906280 http://dx.doi.org/10.3390/cancers12010111 |
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author | Tea, Melinda N. Poonnoose, Santosh I. Pitson, Stuart M. |
author_facet | Tea, Melinda N. Poonnoose, Santosh I. Pitson, Stuart M. |
author_sort | Tea, Melinda N. |
collection | PubMed |
description | Glioblastoma (GBM) is the most commonly diagnosed malignant brain tumor in adults. The prognosis for patients with GBM remains poor and largely unchanged over the last 30 years, due to the limitations of existing therapies. Thus, new therapeutic approaches are desperately required. Sphingolipids are highly enriched in the brain, forming the structural components of cell membranes, and are major lipid constituents of the myelin sheaths of nerve axons, as well as playing critical roles in cell signaling. Indeed, a number of sphingolipids elicit a variety of cellular responses involved in the development and progression of GBM. Here, we discuss the role of sphingolipids in the pathobiology of GBM, and how targeting sphingolipid metabolism has emerged as a promising approach for the treatment of GBM. |
format | Online Article Text |
id | pubmed-7017054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70170542020-02-28 Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma Tea, Melinda N. Poonnoose, Santosh I. Pitson, Stuart M. Cancers (Basel) Review Glioblastoma (GBM) is the most commonly diagnosed malignant brain tumor in adults. The prognosis for patients with GBM remains poor and largely unchanged over the last 30 years, due to the limitations of existing therapies. Thus, new therapeutic approaches are desperately required. Sphingolipids are highly enriched in the brain, forming the structural components of cell membranes, and are major lipid constituents of the myelin sheaths of nerve axons, as well as playing critical roles in cell signaling. Indeed, a number of sphingolipids elicit a variety of cellular responses involved in the development and progression of GBM. Here, we discuss the role of sphingolipids in the pathobiology of GBM, and how targeting sphingolipid metabolism has emerged as a promising approach for the treatment of GBM. MDPI 2020-01-01 /pmc/articles/PMC7017054/ /pubmed/31906280 http://dx.doi.org/10.3390/cancers12010111 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Tea, Melinda N. Poonnoose, Santosh I. Pitson, Stuart M. Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma |
title | Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma |
title_full | Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma |
title_fullStr | Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma |
title_full_unstemmed | Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma |
title_short | Targeting the Sphingolipid System as a Therapeutic Direction for Glioblastoma |
title_sort | targeting the sphingolipid system as a therapeutic direction for glioblastoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017054/ https://www.ncbi.nlm.nih.gov/pubmed/31906280 http://dx.doi.org/10.3390/cancers12010111 |
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