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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7072318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT morrishemma futuretherapeuticdirectionsforsmacmimetics AT brumattigabriela futuretherapeuticdirectionsforsmacmimetics AT silkejohn futuretherapeuticdirectionsforsmacmimetics |