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TRAIL combinations: The new ‘trail’ for cancer therapy (Review)
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) therapy is anticipated to be one of the most effective cancer treatments. However, resistance to TRAIL therapy remains a challenge facing the development of anticancer strategies. To circumvent this problem, TRAIL combinations have been...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997674/ https://www.ncbi.nlm.nih.gov/pubmed/24765133 http://dx.doi.org/10.3892/ol.2014.1922 |
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author | REFAAT, ALAA ABD-RABOU, AHMED REDA, ASMAA |
author_facet | REFAAT, ALAA ABD-RABOU, AHMED REDA, ASMAA |
author_sort | REFAAT, ALAA |
collection | PubMed |
description | Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) therapy is anticipated to be one of the most effective cancer treatments. However, resistance to TRAIL therapy remains a challenge facing the development of anticancer strategies. To circumvent this problem, TRAIL combinations have been experimented with for over ten years to induce synergism or sensitize resistant cancer cells. By analyzing the signaling pathways triggered by these combinations, this review has defined a set of core targets for novel combinatorial treatments. The review suggests specific pathways to be targeted together with TRAIL for more efficient treatment, including cellular FLICE inhibitory protein and its downstream survival factors, the Bcl-2 family and other prominent targets. The suggested pathways provide new avenues for more effective TRAIL-based cancer therapy. |
format | Online Article Text |
id | pubmed-3997674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-39976742014-04-24 TRAIL combinations: The new ‘trail’ for cancer therapy (Review) REFAAT, ALAA ABD-RABOU, AHMED REDA, ASMAA Oncol Lett Articles Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) therapy is anticipated to be one of the most effective cancer treatments. However, resistance to TRAIL therapy remains a challenge facing the development of anticancer strategies. To circumvent this problem, TRAIL combinations have been experimented with for over ten years to induce synergism or sensitize resistant cancer cells. By analyzing the signaling pathways triggered by these combinations, this review has defined a set of core targets for novel combinatorial treatments. The review suggests specific pathways to be targeted together with TRAIL for more efficient treatment, including cellular FLICE inhibitory protein and its downstream survival factors, the Bcl-2 family and other prominent targets. The suggested pathways provide new avenues for more effective TRAIL-based cancer therapy. D.A. Spandidos 2014-05 2014-02-27 /pmc/articles/PMC3997674/ /pubmed/24765133 http://dx.doi.org/10.3892/ol.2014.1922 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles REFAAT, ALAA ABD-RABOU, AHMED REDA, ASMAA TRAIL combinations: The new ‘trail’ for cancer therapy (Review) |
title | TRAIL combinations: The new ‘trail’ for cancer therapy (Review) |
title_full | TRAIL combinations: The new ‘trail’ for cancer therapy (Review) |
title_fullStr | TRAIL combinations: The new ‘trail’ for cancer therapy (Review) |
title_full_unstemmed | TRAIL combinations: The new ‘trail’ for cancer therapy (Review) |
title_short | TRAIL combinations: The new ‘trail’ for cancer therapy (Review) |
title_sort | trail combinations: the new ‘trail’ for cancer therapy (review) |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997674/ https://www.ncbi.nlm.nih.gov/pubmed/24765133 http://dx.doi.org/10.3892/ol.2014.1922 |
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