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Death receptors as targets for anti-cancer therapy

Human tumour cells are characterized by their ability to avoid the normal regulatory mechanisms of cell growth, division and death. The classical chemotherapy aims to kill tumour cells by causing DNA damage-induced apoptosis. However, as many tumour cells posses mutations in intracellular apoptosis-...

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Detalles Bibliográficos
Autores principales: Papenfuss, Kerstin, Cordier, Stefanie M, Walczak, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828874/
https://www.ncbi.nlm.nih.gov/pubmed/19210756
http://dx.doi.org/10.1111/j.1582-4934.2008.00514.x
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author Papenfuss, Kerstin
Cordier, Stefanie M
Walczak, Henning
author_facet Papenfuss, Kerstin
Cordier, Stefanie M
Walczak, Henning
author_sort Papenfuss, Kerstin
collection PubMed
description Human tumour cells are characterized by their ability to avoid the normal regulatory mechanisms of cell growth, division and death. The classical chemotherapy aims to kill tumour cells by causing DNA damage-induced apoptosis. However, as many tumour cells posses mutations in intracellular apoptosis-sensing molecules like p53, they are not capable of inducing apoptosis on their own and are therefore resistant to chemotherapy. With the discovery of the death receptors the opportunity arose to directly trigger apoptosis from the outside of tumour cells, thereby circumventing chemotherapeutic resistance. Death receptors belong to the tumour necrosis factor receptor superfamily, with tumour necrosis factor (TNF) receptor-1, CD95 and TNF-related apoptosis-inducing ligand-R1 and -R2 being the most prominent members. This review covers the current knowledge about these four death receptors, summarizes pre-clinical approaches engaging these death receptors in anti-cancer therapy and also gives an overview about their application in clinical trials conducted to date.
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spelling pubmed-38288742015-04-27 Death receptors as targets for anti-cancer therapy Papenfuss, Kerstin Cordier, Stefanie M Walczak, Henning J Cell Mol Med Reviews Human tumour cells are characterized by their ability to avoid the normal regulatory mechanisms of cell growth, division and death. The classical chemotherapy aims to kill tumour cells by causing DNA damage-induced apoptosis. However, as many tumour cells posses mutations in intracellular apoptosis-sensing molecules like p53, they are not capable of inducing apoptosis on their own and are therefore resistant to chemotherapy. With the discovery of the death receptors the opportunity arose to directly trigger apoptosis from the outside of tumour cells, thereby circumventing chemotherapeutic resistance. Death receptors belong to the tumour necrosis factor receptor superfamily, with tumour necrosis factor (TNF) receptor-1, CD95 and TNF-related apoptosis-inducing ligand-R1 and -R2 being the most prominent members. This review covers the current knowledge about these four death receptors, summarizes pre-clinical approaches engaging these death receptors in anti-cancer therapy and also gives an overview about their application in clinical trials conducted to date. Blackwell Publishing Ltd 2008-12 2008-10-06 /pmc/articles/PMC3828874/ /pubmed/19210756 http://dx.doi.org/10.1111/j.1582-4934.2008.00514.x Text en © 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Reviews
Papenfuss, Kerstin
Cordier, Stefanie M
Walczak, Henning
Death receptors as targets for anti-cancer therapy
title Death receptors as targets for anti-cancer therapy
title_full Death receptors as targets for anti-cancer therapy
title_fullStr Death receptors as targets for anti-cancer therapy
title_full_unstemmed Death receptors as targets for anti-cancer therapy
title_short Death receptors as targets for anti-cancer therapy
title_sort death receptors as targets for anti-cancer therapy
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828874/
https://www.ncbi.nlm.nih.gov/pubmed/19210756
http://dx.doi.org/10.1111/j.1582-4934.2008.00514.x
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