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On BH3 Mimetics and Ca(2+) Signaling

[Table: see text] BH3 mimetics are anticancer agents that reproduce the spatial arrangement of the BH3 domain of Bcl‐2 family proteins. Just like the BH3‐only proteins, these compounds bind to the hydrophobic cleft of the pro‐survival Bcl‐2 members such as Bcl‐2 or Bcl‐xL, and disrupt their heterodi...

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Detalles Bibliográficos
Autores principales: Ferdek, Pawel E., Jakubowska, Monika A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601233/
https://www.ncbi.nlm.nih.gov/pubmed/28804913
http://dx.doi.org/10.1002/ddr.21405
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author Ferdek, Pawel E.
Jakubowska, Monika A.
author_facet Ferdek, Pawel E.
Jakubowska, Monika A.
author_sort Ferdek, Pawel E.
collection PubMed
description [Table: see text] BH3 mimetics are anticancer agents that reproduce the spatial arrangement of the BH3 domain of Bcl‐2 family proteins. Just like the BH3‐only proteins, these compounds bind to the hydrophobic cleft of the pro‐survival Bcl‐2 members such as Bcl‐2 or Bcl‐xL, and disrupt their heterodimerization with pro‐apoptotic Bax or Bak, sensitizing cells to chemotherapy. In recent years, it has become clear that Bcl‐2 family proteins are engaged in regulation of intracellular Ca(2+) homeostasis, including Ca(2+) release from the intracellular stores as well as Ca(2+) fluxes across the plasma membrane. Given that BH3 mimetics shift the balance between the prosurvival and proapoptotic Bcl‐2 members, they might indirectly exert effects on intracellular Ca(2+) signals. Indeed, it has been reported that some BH3 mimetics release Ca(2+) from the intracellular stores causing Ca(2+) overload in the cytosol. Therefore, the effects of any new BH3 mimetics on cellular Ca(2+) homeostasis should be tested before these compounds progress to clinical trials. Drug Dev Res 78 : 313–318, 2017. © 2017 Wiley Periodicals, Inc.
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spelling pubmed-56012332017-10-03 On BH3 Mimetics and Ca(2+) Signaling Ferdek, Pawel E. Jakubowska, Monika A. Drug Dev Res Research Commentary [Table: see text] BH3 mimetics are anticancer agents that reproduce the spatial arrangement of the BH3 domain of Bcl‐2 family proteins. Just like the BH3‐only proteins, these compounds bind to the hydrophobic cleft of the pro‐survival Bcl‐2 members such as Bcl‐2 or Bcl‐xL, and disrupt their heterodimerization with pro‐apoptotic Bax or Bak, sensitizing cells to chemotherapy. In recent years, it has become clear that Bcl‐2 family proteins are engaged in regulation of intracellular Ca(2+) homeostasis, including Ca(2+) release from the intracellular stores as well as Ca(2+) fluxes across the plasma membrane. Given that BH3 mimetics shift the balance between the prosurvival and proapoptotic Bcl‐2 members, they might indirectly exert effects on intracellular Ca(2+) signals. Indeed, it has been reported that some BH3 mimetics release Ca(2+) from the intracellular stores causing Ca(2+) overload in the cytosol. Therefore, the effects of any new BH3 mimetics on cellular Ca(2+) homeostasis should be tested before these compounds progress to clinical trials. Drug Dev Res 78 : 313–318, 2017. © 2017 Wiley Periodicals, Inc. John Wiley and Sons Inc. 2017-08-13 2017-09 /pmc/articles/PMC5601233/ /pubmed/28804913 http://dx.doi.org/10.1002/ddr.21405 Text en © 2017 The Authors Drug Development Research Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Commentary
Ferdek, Pawel E.
Jakubowska, Monika A.
On BH3 Mimetics and Ca(2+) Signaling
title On BH3 Mimetics and Ca(2+) Signaling
title_full On BH3 Mimetics and Ca(2+) Signaling
title_fullStr On BH3 Mimetics and Ca(2+) Signaling
title_full_unstemmed On BH3 Mimetics and Ca(2+) Signaling
title_short On BH3 Mimetics and Ca(2+) Signaling
title_sort on bh3 mimetics and ca(2+) signaling
topic Research Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601233/
https://www.ncbi.nlm.nih.gov/pubmed/28804913
http://dx.doi.org/10.1002/ddr.21405
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