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Apoptosis pathways and their therapeutic exploitation in pancreatic cancer
Resistance to apoptosis (programmed cell death) is a characteristic feature of human malignancies including pancreatic cancer, which is one of the leading causes of cancer deaths in the western world. Defects in this intrinsic cell death program can contribute to the multistep process of tumorigenes...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496136/ https://www.ncbi.nlm.nih.gov/pubmed/19382915 http://dx.doi.org/10.1111/j.1582-4934.2009.00748.x |
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author | Fulda, Simone |
author_facet | Fulda, Simone |
author_sort | Fulda, Simone |
collection | PubMed |
description | Resistance to apoptosis (programmed cell death) is a characteristic feature of human malignancies including pancreatic cancer, which is one of the leading causes of cancer deaths in the western world. Defects in this intrinsic cell death program can contribute to the multistep process of tumorigenesis, because too little cell death can disturb tissue homeostasis. Further, blockade of apoptosis pathways can cause treatment failure, because intact apoptosis signalling cascades largely mediate therapy-induced cytotoxicity. The elucidation of apoptosis pathways in pancreatic carcinoma over the last decade has resulted in the identification of various molecular defects. How apoptosis pathways can be exploited for the treatment of pancreatic cancer will be discussed in this review. |
format | Online Article Text |
id | pubmed-4496136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44961362015-07-13 Apoptosis pathways and their therapeutic exploitation in pancreatic cancer Fulda, Simone J Cell Mol Med Reviews Resistance to apoptosis (programmed cell death) is a characteristic feature of human malignancies including pancreatic cancer, which is one of the leading causes of cancer deaths in the western world. Defects in this intrinsic cell death program can contribute to the multistep process of tumorigenesis, because too little cell death can disturb tissue homeostasis. Further, blockade of apoptosis pathways can cause treatment failure, because intact apoptosis signalling cascades largely mediate therapy-induced cytotoxicity. The elucidation of apoptosis pathways in pancreatic carcinoma over the last decade has resulted in the identification of various molecular defects. How apoptosis pathways can be exploited for the treatment of pancreatic cancer will be discussed in this review. John Wiley & Sons, Ltd 2009-07 2009-03-27 /pmc/articles/PMC4496136/ /pubmed/19382915 http://dx.doi.org/10.1111/j.1582-4934.2009.00748.x Text en © 2009 The Author Journal compilation © 2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd |
spellingShingle | Reviews Fulda, Simone Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
title | Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
title_full | Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
title_fullStr | Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
title_full_unstemmed | Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
title_short | Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
title_sort | apoptosis pathways and their therapeutic exploitation in pancreatic cancer |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496136/ https://www.ncbi.nlm.nih.gov/pubmed/19382915 http://dx.doi.org/10.1111/j.1582-4934.2009.00748.x |
work_keys_str_mv | AT fuldasimone apoptosispathwaysandtheirtherapeuticexploitationinpancreaticcancer |