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Recent advances in understanding inhibitor of apoptosis proteins
The inhibitor of apoptosis proteins (IAPs) are a family of proteins that were chiefly known for their ability to inhibit apoptosis by blocking caspase activation or activity. Recent research has shown that cellular IAP1 (cIAP1), cIAP2, and X-linked IAP (XIAP) also regulate signaling by receptors of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281012/ https://www.ncbi.nlm.nih.gov/pubmed/30631429 http://dx.doi.org/10.12688/f1000research.16439.1 |
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author | Lalaoui, Najoua Vaux, David Lawrence |
author_facet | Lalaoui, Najoua Vaux, David Lawrence |
author_sort | Lalaoui, Najoua |
collection | PubMed |
description | The inhibitor of apoptosis proteins (IAPs) are a family of proteins that were chiefly known for their ability to inhibit apoptosis by blocking caspase activation or activity. Recent research has shown that cellular IAP1 (cIAP1), cIAP2, and X-linked IAP (XIAP) also regulate signaling by receptors of the innate immune system by ubiquitylating their substrates. These IAPs thereby act at the intersection of pathways leading to cell death and inflammation. Mutation of IAP genes can impair tissue homeostasis and is linked to several human diseases. Small-molecule IAP antagonists have been developed to treat certain malignant, infectious, and inflammatory diseases. Here, we will discuss recent advances in our understanding of the functions of cIAP1, cIAP2, and XIAP; the consequences of their mutation or dysregulation; and the therapeutic potential of IAP antagonist drugs. |
format | Online Article Text |
id | pubmed-6281012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-62810122019-01-09 Recent advances in understanding inhibitor of apoptosis proteins Lalaoui, Najoua Vaux, David Lawrence F1000Res Review The inhibitor of apoptosis proteins (IAPs) are a family of proteins that were chiefly known for their ability to inhibit apoptosis by blocking caspase activation or activity. Recent research has shown that cellular IAP1 (cIAP1), cIAP2, and X-linked IAP (XIAP) also regulate signaling by receptors of the innate immune system by ubiquitylating their substrates. These IAPs thereby act at the intersection of pathways leading to cell death and inflammation. Mutation of IAP genes can impair tissue homeostasis and is linked to several human diseases. Small-molecule IAP antagonists have been developed to treat certain malignant, infectious, and inflammatory diseases. Here, we will discuss recent advances in our understanding of the functions of cIAP1, cIAP2, and XIAP; the consequences of their mutation or dysregulation; and the therapeutic potential of IAP antagonist drugs. F1000 Research Limited 2018-12-03 /pmc/articles/PMC6281012/ /pubmed/30631429 http://dx.doi.org/10.12688/f1000research.16439.1 Text en Copyright: © 2018 Lalaoui N and Vaux DL http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Lalaoui, Najoua Vaux, David Lawrence Recent advances in understanding inhibitor of apoptosis proteins |
title | Recent advances in understanding inhibitor of apoptosis proteins |
title_full | Recent advances in understanding inhibitor of apoptosis proteins |
title_fullStr | Recent advances in understanding inhibitor of apoptosis proteins |
title_full_unstemmed | Recent advances in understanding inhibitor of apoptosis proteins |
title_short | Recent advances in understanding inhibitor of apoptosis proteins |
title_sort | recent advances in understanding inhibitor of apoptosis proteins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281012/ https://www.ncbi.nlm.nih.gov/pubmed/30631429 http://dx.doi.org/10.12688/f1000research.16439.1 |
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