Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives

Necroptosis is a caspases-independent programmed cell death displaying intermediate features between necrosis and apoptosis. Albeit some physiological roles during embryonic development such tissue homeostasis and innate immune response are documented, necroptosis is mainly considered a pro-inflamma...

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Main Authors: Anna Negroni, Eleonora Colantoni, Salvatore Cucchiara, Laura Stronati
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/10/10/1431
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spelling doaj-a03867c4b2744ce391f9e93195c57ca92020-11-25T03:43:53ZengMDPI AGBiomolecules2218-273X2020-10-01101431143110.3390/biom10101431Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic PerspectivesAnna Negroni0Eleonora Colantoni1Salvatore Cucchiara2Laura Stronati3Division of Health Protection Technologies, ENEA, 00123 Rome, ItalyMaternal Infantile and Urological Sciences Department, Sapienza University of Rome, 00161 Rome, ItalyMaternal Infantile and Urological Sciences Department, Sapienza University of Rome, 00161 Rome, ItalyDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, ItalyNecroptosis is a caspases-independent programmed cell death displaying intermediate features between necrosis and apoptosis. Albeit some physiological roles during embryonic development such tissue homeostasis and innate immune response are documented, necroptosis is mainly considered a pro-inflammatory cell death. Key actors of necroptosis are the receptor-interacting-protein-kinases, RIPK1 and RIPK3, and their target, the mixed-lineage-kinase-domain-like protein, MLKL. The intestinal epithelium has one of the highest rates of cellular turnover in a process that is tightly regulated. Altered necroptosis at the intestinal epithelium leads to uncontrolled microbial translocation and deleterious inflammation. Indeed, necroptosis plays a role in many disease conditions and inhibiting necroptosis is currently considered a promising therapeutic strategy. In this review, we focus on the molecular mechanisms of necroptosis as well as its involvement in human diseases. We also discuss the present developing therapies that target necroptosis machinery.https://www.mdpi.com/2218-273X/10/10/1431programmed cell deathinflammationcancerintestinal diseasesinhibitors
collection DOAJ
language English
format Article
sources DOAJ
author Anna Negroni
Eleonora Colantoni
Salvatore Cucchiara
Laura Stronati
spellingShingle Anna Negroni
Eleonora Colantoni
Salvatore Cucchiara
Laura Stronati
Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives
Biomolecules
programmed cell death
inflammation
cancer
intestinal diseases
inhibitors
author_facet Anna Negroni
Eleonora Colantoni
Salvatore Cucchiara
Laura Stronati
author_sort Anna Negroni
title Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives
title_short Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives
title_full Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives
title_fullStr Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives
title_full_unstemmed Necroptosis in Intestinal Inflammation and Cancer: New Concepts and Therapeutic Perspectives
title_sort necroptosis in intestinal inflammation and cancer: new concepts and therapeutic perspectives
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2020-10-01
description Necroptosis is a caspases-independent programmed cell death displaying intermediate features between necrosis and apoptosis. Albeit some physiological roles during embryonic development such tissue homeostasis and innate immune response are documented, necroptosis is mainly considered a pro-inflammatory cell death. Key actors of necroptosis are the receptor-interacting-protein-kinases, RIPK1 and RIPK3, and their target, the mixed-lineage-kinase-domain-like protein, MLKL. The intestinal epithelium has one of the highest rates of cellular turnover in a process that is tightly regulated. Altered necroptosis at the intestinal epithelium leads to uncontrolled microbial translocation and deleterious inflammation. Indeed, necroptosis plays a role in many disease conditions and inhibiting necroptosis is currently considered a promising therapeutic strategy. In this review, we focus on the molecular mechanisms of necroptosis as well as its involvement in human diseases. We also discuss the present developing therapies that target necroptosis machinery.
topic programmed cell death
inflammation
cancer
intestinal diseases
inhibitors
url https://www.mdpi.com/2218-273X/10/10/1431
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