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Reversibility of apoptosis in cancer cells

Apoptosis is a cell suicide programme characterised by unique cellular events such as mitochondrial fragmentation and dysfunction, nuclear condensation, cytoplasmic shrinkage and activation of apoptotic protease caspases, and these serve as the noticeable apoptotic markers for the commitment of cell...

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Autores principales: Tang, H L, Yuen, K L, Tang, H M, Fung, M C
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2634673/
https://www.ncbi.nlm.nih.gov/pubmed/19088725
http://dx.doi.org/10.1038/sj.bjc.6604802
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author Tang, H L
Yuen, K L
Tang, H M
Fung, M C
author_facet Tang, H L
Yuen, K L
Tang, H M
Fung, M C
author_sort Tang, H L
collection PubMed
description Apoptosis is a cell suicide programme characterised by unique cellular events such as mitochondrial fragmentation and dysfunction, nuclear condensation, cytoplasmic shrinkage and activation of apoptotic protease caspases, and these serve as the noticeable apoptotic markers for the commitment of cell demise. Here, we show that, however, the characterised apoptotic dying cancer cells can regain their normal morphology and proliferate after removal of apoptotic inducers. In addition, we demonstrate that reversibility of apoptosis occurs in various cancer cell lines, and in different apoptotic stimuli. Our findings show that cancer cells can survive after initiation of apoptosis, thereby revealing an unexpected potential escape mechanism of cancer cells from chemotherapy.
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spelling pubmed-26346732010-01-13 Reversibility of apoptosis in cancer cells Tang, H L Yuen, K L Tang, H M Fung, M C Br J Cancer Molecular Diagnostics Apoptosis is a cell suicide programme characterised by unique cellular events such as mitochondrial fragmentation and dysfunction, nuclear condensation, cytoplasmic shrinkage and activation of apoptotic protease caspases, and these serve as the noticeable apoptotic markers for the commitment of cell demise. Here, we show that, however, the characterised apoptotic dying cancer cells can regain their normal morphology and proliferate after removal of apoptotic inducers. In addition, we demonstrate that reversibility of apoptosis occurs in various cancer cell lines, and in different apoptotic stimuli. Our findings show that cancer cells can survive after initiation of apoptosis, thereby revealing an unexpected potential escape mechanism of cancer cells from chemotherapy. Nature Publishing Group 2009-01-13 2008-12-16 /pmc/articles/PMC2634673/ /pubmed/19088725 http://dx.doi.org/10.1038/sj.bjc.6604802 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Tang, H L
Yuen, K L
Tang, H M
Fung, M C
Reversibility of apoptosis in cancer cells
title Reversibility of apoptosis in cancer cells
title_full Reversibility of apoptosis in cancer cells
title_fullStr Reversibility of apoptosis in cancer cells
title_full_unstemmed Reversibility of apoptosis in cancer cells
title_short Reversibility of apoptosis in cancer cells
title_sort reversibility of apoptosis in cancer cells
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2634673/
https://www.ncbi.nlm.nih.gov/pubmed/19088725
http://dx.doi.org/10.1038/sj.bjc.6604802
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