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New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy

Caspase activation has been frequently viewed as synonymous with programmed cell death (PCcD); however, accumulating evidence showed that there existing caspase-independent PCcD pathways displaying morphologies that are not fully consistent with classical apoptosis. In this article, we will focus on...

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Detalles Bibliográficos
Autores principales: Qi, Rong, Liu, Xin Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Master Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614612/
https://www.ncbi.nlm.nih.gov/pubmed/23674984
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author Qi, Rong
Liu, Xin Yuan
author_facet Qi, Rong
Liu, Xin Yuan
author_sort Qi, Rong
collection PubMed
description Caspase activation has been frequently viewed as synonymous with programmed cell death (PCcD); however, accumulating evidence showed that there existing caspase-independent PCcD pathways displaying morphologies that are not fully consistent with classical apoptosis. In this article, we will focus on the most recent progresses of different models of PCcD independent of caspases activity. Since some tumor cells can unexpectedly survive the activation of caspases, and tumor suppressor proteins that activate caspase-independent PCcD are commonly mutated in human cancer, the alternative cell death pathways are gaining increasing interest among cancer researchers. Though the mechanism of this cell death pathway is poorly understood, it is clear that a full understanding of the regulation of caspase-independent PCcD could provide new means of improving current diagnosis and promoting conceptual advances for the design of new therapeutic strategies for cancer therapy.
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spelling pubmed-36146122013-05-01 New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy Qi, Rong Liu, Xin Yuan Int J Biomed Sci Article Caspase activation has been frequently viewed as synonymous with programmed cell death (PCcD); however, accumulating evidence showed that there existing caspase-independent PCcD pathways displaying morphologies that are not fully consistent with classical apoptosis. In this article, we will focus on the most recent progresses of different models of PCcD independent of caspases activity. Since some tumor cells can unexpectedly survive the activation of caspases, and tumor suppressor proteins that activate caspase-independent PCcD are commonly mutated in human cancer, the alternative cell death pathways are gaining increasing interest among cancer researchers. Though the mechanism of this cell death pathway is poorly understood, it is clear that a full understanding of the regulation of caspase-independent PCcD could provide new means of improving current diagnosis and promoting conceptual advances for the design of new therapeutic strategies for cancer therapy. Master Publishing Group 2006-09 /pmc/articles/PMC3614612/ /pubmed/23674984 Text en © Qi et al. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Qi, Rong
Liu, Xin Yuan
New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy
title New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy
title_full New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy
title_fullStr New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy
title_full_unstemmed New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy
title_short New Advance in Caspase-Independent Programmed Cell Death and its Potential in Cancer Therapy
title_sort new advance in caspase-independent programmed cell death and its potential in cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614612/
https://www.ncbi.nlm.nih.gov/pubmed/23674984
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