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Future Therapeutic Directions for Smac-Mimetics

It is well accepted that the ability of cancer cells to circumvent the cell death program that untransformed cells are subject to helps promote tumor growth. Strategies designed to reinstate the cell death program in cancer cells have therefore been investigated for decades. Overexpression of member...

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Autores principales: Morrish, Emma, Brumatti, Gabriela, Silke, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072318/
https://www.ncbi.nlm.nih.gov/pubmed/32053868
http://dx.doi.org/10.3390/cells9020406
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author Morrish, Emma
Brumatti, Gabriela
Silke, John
author_facet Morrish, Emma
Brumatti, Gabriela
Silke, John
author_sort Morrish, Emma
collection PubMed
description It is well accepted that the ability of cancer cells to circumvent the cell death program that untransformed cells are subject to helps promote tumor growth. Strategies designed to reinstate the cell death program in cancer cells have therefore been investigated for decades. Overexpression of members of the Inhibitor of APoptosis (IAP) protein family is one possible mechanism hindering the death of cancer cells. To promote cell death, drugs that mimic natural IAP antagonists, such as second mitochondria-derived activator of caspases (Smac/DIABLO) were developed. Smac-Mimetics (SMs) have entered clinical trials for hematological and solid cancers, unfortunately with variable and limited results so far. This review explores the use of SMs for the treatment of cancer, their potential to synergize with up-coming treatments and, finally, discusses the challenges and optimism facing this strategy.
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spelling pubmed-70723182020-03-19 Future Therapeutic Directions for Smac-Mimetics Morrish, Emma Brumatti, Gabriela Silke, John Cells Review It is well accepted that the ability of cancer cells to circumvent the cell death program that untransformed cells are subject to helps promote tumor growth. Strategies designed to reinstate the cell death program in cancer cells have therefore been investigated for decades. Overexpression of members of the Inhibitor of APoptosis (IAP) protein family is one possible mechanism hindering the death of cancer cells. To promote cell death, drugs that mimic natural IAP antagonists, such as second mitochondria-derived activator of caspases (Smac/DIABLO) were developed. Smac-Mimetics (SMs) have entered clinical trials for hematological and solid cancers, unfortunately with variable and limited results so far. This review explores the use of SMs for the treatment of cancer, their potential to synergize with up-coming treatments and, finally, discusses the challenges and optimism facing this strategy. MDPI 2020-02-11 /pmc/articles/PMC7072318/ /pubmed/32053868 http://dx.doi.org/10.3390/cells9020406 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
Morrish, Emma
Brumatti, Gabriela
Silke, John
Future Therapeutic Directions for Smac-Mimetics
title Future Therapeutic Directions for Smac-Mimetics
title_full Future Therapeutic Directions for Smac-Mimetics
title_fullStr Future Therapeutic Directions for Smac-Mimetics
title_full_unstemmed Future Therapeutic Directions for Smac-Mimetics
title_short Future Therapeutic Directions for Smac-Mimetics
title_sort future therapeutic directions for smac-mimetics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072318/
https://www.ncbi.nlm.nih.gov/pubmed/32053868
http://dx.doi.org/10.3390/cells9020406
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