Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Fulda, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
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
_version_ 1782282081717452800
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