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Leaving the lysosome behind: novel developments in autophagy inhibition

The search for a single silver bullet for the treatment of cancer has now been overshadowed by the identification of multiple therapeutic targets unique to each malignancy and even to each patient. In recent years, autophagy has emerged as one such therapeutic target. In response to both therapeutic...

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Detalles Bibliográficos
Autores principales: Solitro, Abigail R, MacKeigan, Jeffrey P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886745/
https://www.ncbi.nlm.nih.gov/pubmed/26689099
http://dx.doi.org/10.4155/fmc.15.166
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author Solitro, Abigail R
MacKeigan, Jeffrey P
author_facet Solitro, Abigail R
MacKeigan, Jeffrey P
author_sort Solitro, Abigail R
collection PubMed
description The search for a single silver bullet for the treatment of cancer has now been overshadowed by the identification of multiple therapeutic targets unique to each malignancy and even to each patient. In recent years, autophagy has emerged as one such therapeutic target. In response to both therapeutic and oncogenic stress, cancer cells upregulate and demonstrate an increased dependence upon this intracellular recycling process. Particularly in malignancies that currently lack targeted therapeutic options, autophagy inhibitors are the next hopeful prospects for the treatment of this disease. In this review, we discuss the rapid evolution of autophagy inhibitors from early lysosomotropic agents to next-generation lysosome-targeted drugs and beyond.
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spelling pubmed-48867452016-05-31 Leaving the lysosome behind: novel developments in autophagy inhibition Solitro, Abigail R MacKeigan, Jeffrey P Future Med Chem Review The search for a single silver bullet for the treatment of cancer has now been overshadowed by the identification of multiple therapeutic targets unique to each malignancy and even to each patient. In recent years, autophagy has emerged as one such therapeutic target. In response to both therapeutic and oncogenic stress, cancer cells upregulate and demonstrate an increased dependence upon this intracellular recycling process. Particularly in malignancies that currently lack targeted therapeutic options, autophagy inhibitors are the next hopeful prospects for the treatment of this disease. In this review, we discuss the rapid evolution of autophagy inhibitors from early lysosomotropic agents to next-generation lysosome-targeted drugs and beyond. Future Science Ltd 2016-01 /pmc/articles/PMC4886745/ /pubmed/26689099 http://dx.doi.org/10.4155/fmc.15.166 Text en © 2016 Abigail R. Solitro This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
Solitro, Abigail R
MacKeigan, Jeffrey P
Leaving the lysosome behind: novel developments in autophagy inhibition
title Leaving the lysosome behind: novel developments in autophagy inhibition
title_full Leaving the lysosome behind: novel developments in autophagy inhibition
title_fullStr Leaving the lysosome behind: novel developments in autophagy inhibition
title_full_unstemmed Leaving the lysosome behind: novel developments in autophagy inhibition
title_short Leaving the lysosome behind: novel developments in autophagy inhibition
title_sort leaving the lysosome behind: novel developments in autophagy inhibition
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886745/
https://www.ncbi.nlm.nih.gov/pubmed/26689099
http://dx.doi.org/10.4155/fmc.15.166
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