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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...

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Detalles Bibliográficos
Autores principales: Lalaoui, Najoua, Vaux, David Lawrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
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.
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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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