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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...

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Detalles Bibliográficos
Autores principales: REFAAT, ALAA, ABD-RABOU, AHMED, REDA, ASMAA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
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.
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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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