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Development of targeted therapies in treatment of glioblastoma
Glioblastoma (GBM) is a type of tumor that is highly lethal despite maximal therapy. Standard therapeutic approaches provide modest improvement in progression-free and overall survival, necessitating the investigation of novel therapies. Oncologic therapy has recently experienced a rapid evolution t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Anti-Cancer Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607828/ https://www.ncbi.nlm.nih.gov/pubmed/26487967 http://dx.doi.org/10.7497/j.issn.2095-3941.2015.0020 |
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author | Xu, Yuan-Yuan Gao, Pei Sun, Ying Duan, You-Rong |
author_facet | Xu, Yuan-Yuan Gao, Pei Sun, Ying Duan, You-Rong |
author_sort | Xu, Yuan-Yuan |
collection | PubMed |
description | Glioblastoma (GBM) is a type of tumor that is highly lethal despite maximal therapy. Standard therapeutic approaches provide modest improvement in progression-free and overall survival, necessitating the investigation of novel therapies. Oncologic therapy has recently experienced a rapid evolution toward “targeted therapy”, with drugs directed against specific targets which play essential roles in the proliferation, survival, and invasiveness of GBM cells, including numerous molecules involved in signal transduction pathways. Inhibitors of these molecules have already entered or are undergoing clinical trials. However, significant challenges in their development remain because several preclinical and clinical studies present conflicting results. In this article, we will provide an up-to-date review of the current targeted therapies in GBM. |
format | Online Article Text |
id | pubmed-4607828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Chinese Anti-Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-46078282015-10-20 Development of targeted therapies in treatment of glioblastoma Xu, Yuan-Yuan Gao, Pei Sun, Ying Duan, You-Rong Cancer Biol Med Review Glioblastoma (GBM) is a type of tumor that is highly lethal despite maximal therapy. Standard therapeutic approaches provide modest improvement in progression-free and overall survival, necessitating the investigation of novel therapies. Oncologic therapy has recently experienced a rapid evolution toward “targeted therapy”, with drugs directed against specific targets which play essential roles in the proliferation, survival, and invasiveness of GBM cells, including numerous molecules involved in signal transduction pathways. Inhibitors of these molecules have already entered or are undergoing clinical trials. However, significant challenges in their development remain because several preclinical and clinical studies present conflicting results. In this article, we will provide an up-to-date review of the current targeted therapies in GBM. Chinese Anti-Cancer Association 2015-09 /pmc/articles/PMC4607828/ /pubmed/26487967 http://dx.doi.org/10.7497/j.issn.2095-3941.2015.0020 Text en 2015 Cancer Biology & Medicine This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Review Xu, Yuan-Yuan Gao, Pei Sun, Ying Duan, You-Rong Development of targeted therapies in treatment of glioblastoma |
title | Development of targeted therapies in treatment of glioblastoma |
title_full | Development of targeted therapies in treatment of glioblastoma |
title_fullStr | Development of targeted therapies in treatment of glioblastoma |
title_full_unstemmed | Development of targeted therapies in treatment of glioblastoma |
title_short | Development of targeted therapies in treatment of glioblastoma |
title_sort | development of targeted therapies in treatment of glioblastoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607828/ https://www.ncbi.nlm.nih.gov/pubmed/26487967 http://dx.doi.org/10.7497/j.issn.2095-3941.2015.0020 |
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