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Emerging approaches to target mitochondrial apoptosis in cancer cells

Apoptosis is a highly conserved programme for removing damaged and unwanted cells. Apoptosis in most cells is coordinated on mitochondria by the Bcl-2 family of proteins. The balance between pro- and anti-apoptotic Bcl-2 family proteins sets a threshold for mitochondrial apoptosis, a balance that is...

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Detalles Bibliográficos
Autores principales: Gilmore, Andrew, King, Louise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816453/
https://www.ncbi.nlm.nih.gov/pubmed/31681471
http://dx.doi.org/10.12688/f1000research.18872.1
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author Gilmore, Andrew
King, Louise
author_facet Gilmore, Andrew
King, Louise
author_sort Gilmore, Andrew
collection PubMed
description Apoptosis is a highly conserved programme for removing damaged and unwanted cells. Apoptosis in most cells is coordinated on mitochondria by the Bcl-2 family of proteins. The balance between pro- and anti-apoptotic Bcl-2 family proteins sets a threshold for mitochondrial apoptosis, a balance that is altered during cancer progression. Consequently, avoidance of cell death is an established cancer hallmark. Although there is a general perception that tumour cells are more resistant to apoptosis than their normal counterparts, the realities of cell death regulation in cancer are more nuanced. In this review we discuss how a profound understanding of this control has led to new therapeutic approaches, including the new class of BH3-mimetics, which directly target apoptosis as a vulnerability in cancer. We discuss recent findings that highlight the current limitations in our understanding of apoptosis and how these novel therapeutics work.
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spelling pubmed-68164532019-10-31 Emerging approaches to target mitochondrial apoptosis in cancer cells Gilmore, Andrew King, Louise F1000Res Review Apoptosis is a highly conserved programme for removing damaged and unwanted cells. Apoptosis in most cells is coordinated on mitochondria by the Bcl-2 family of proteins. The balance between pro- and anti-apoptotic Bcl-2 family proteins sets a threshold for mitochondrial apoptosis, a balance that is altered during cancer progression. Consequently, avoidance of cell death is an established cancer hallmark. Although there is a general perception that tumour cells are more resistant to apoptosis than their normal counterparts, the realities of cell death regulation in cancer are more nuanced. In this review we discuss how a profound understanding of this control has led to new therapeutic approaches, including the new class of BH3-mimetics, which directly target apoptosis as a vulnerability in cancer. We discuss recent findings that highlight the current limitations in our understanding of apoptosis and how these novel therapeutics work. F1000 Research Limited 2019-10-24 /pmc/articles/PMC6816453/ /pubmed/31681471 http://dx.doi.org/10.12688/f1000research.18872.1 Text en Copyright: © 2019 Gilmore A and King L http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Gilmore, Andrew
King, Louise
Emerging approaches to target mitochondrial apoptosis in cancer cells
title Emerging approaches to target mitochondrial apoptosis in cancer cells
title_full Emerging approaches to target mitochondrial apoptosis in cancer cells
title_fullStr Emerging approaches to target mitochondrial apoptosis in cancer cells
title_full_unstemmed Emerging approaches to target mitochondrial apoptosis in cancer cells
title_short Emerging approaches to target mitochondrial apoptosis in cancer cells
title_sort emerging approaches to target mitochondrial apoptosis in cancer cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816453/
https://www.ncbi.nlm.nih.gov/pubmed/31681471
http://dx.doi.org/10.12688/f1000research.18872.1
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