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Targeting Apoptosis Signaling in Pancreatic Cancer
The ability to escape apoptosis or programmed cell death is a hallmark of human cancers, for example pancreatic cancer. This can promote tumorigenesis, since too little cell death by apoptosis disturbs tissue homeostasis. Additionally, defective apoptosis signaling is the underlying cause of failure...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International (MDPI)
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756359/ https://www.ncbi.nlm.nih.gov/pubmed/24212616 http://dx.doi.org/10.3390/cancers3010241 |
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author | Fulda, Simone |
author_facet | Fulda, Simone |
author_sort | Fulda, Simone |
collection | PubMed |
description | The ability to escape apoptosis or programmed cell death is a hallmark of human cancers, for example pancreatic cancer. This can promote tumorigenesis, since too little cell death by apoptosis disturbs tissue homeostasis. Additionally, defective apoptosis signaling is the underlying cause of failure to respond to current treatment approaches, since therapy-mediated antitumor activity requires the intactness of apoptosis signaling pathways in cancer cells. Thus, the elucidation of defects in the regulation of apoptosis in pancreatic carcinoma can result in the identification of novel targets for therapeutic interference and for exploitation for cancer drug discovery. |
format | Online Article Text |
id | pubmed-3756359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-37563592013-09-04 Targeting Apoptosis Signaling in Pancreatic Cancer Fulda, Simone Cancers (Basel) Review The ability to escape apoptosis or programmed cell death is a hallmark of human cancers, for example pancreatic cancer. This can promote tumorigenesis, since too little cell death by apoptosis disturbs tissue homeostasis. Additionally, defective apoptosis signaling is the underlying cause of failure to respond to current treatment approaches, since therapy-mediated antitumor activity requires the intactness of apoptosis signaling pathways in cancer cells. Thus, the elucidation of defects in the regulation of apoptosis in pancreatic carcinoma can result in the identification of novel targets for therapeutic interference and for exploitation for cancer drug discovery. Molecular Diversity Preservation International (MDPI) 2011-01-11 /pmc/articles/PMC3756359/ /pubmed/24212616 http://dx.doi.org/10.3390/cancers3010241 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Fulda, Simone Targeting Apoptosis Signaling in Pancreatic Cancer |
title | Targeting Apoptosis Signaling in Pancreatic Cancer |
title_full | Targeting Apoptosis Signaling in Pancreatic Cancer |
title_fullStr | Targeting Apoptosis Signaling in Pancreatic Cancer |
title_full_unstemmed | Targeting Apoptosis Signaling in Pancreatic Cancer |
title_short | Targeting Apoptosis Signaling in Pancreatic Cancer |
title_sort | targeting apoptosis signaling in pancreatic cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756359/ https://www.ncbi.nlm.nih.gov/pubmed/24212616 http://dx.doi.org/10.3390/cancers3010241 |
work_keys_str_mv | AT fuldasimone targetingapoptosissignalinginpancreaticcancer |