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Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers

Primary or acquired therapy resistance is a major obstacle to the effective treatment of cancer. Resistance to apoptosis has long been thought to contribute to therapy resistance. We show here that recombinant TRAIL and CDK9 inhibition cooperate in killing cells derived from a broad range of cancers...

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Autores principales: Montinaro, Antonella, Areso Zubiaur, Itziar, Saggau, Julia, Kretz, Anna-Laura, Ferreira, Rute M. M., Hassan, Omar, Kitzig, Ella, Müller, Ines, El-Bahrawy, Mona A., von Karstedt, Silvia, Kulms, Dagmar, Liccardi, Gianmaria, Lemke, Johannes, Walczak, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901660/
https://www.ncbi.nlm.nih.gov/pubmed/34535764
http://dx.doi.org/10.1038/s41418-021-00869-x
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author Montinaro, Antonella
Areso Zubiaur, Itziar
Saggau, Julia
Kretz, Anna-Laura
Ferreira, Rute M. M.
Hassan, Omar
Kitzig, Ella
Müller, Ines
El-Bahrawy, Mona A.
von Karstedt, Silvia
Kulms, Dagmar
Liccardi, Gianmaria
Lemke, Johannes
Walczak, Henning
author_facet Montinaro, Antonella
Areso Zubiaur, Itziar
Saggau, Julia
Kretz, Anna-Laura
Ferreira, Rute M. M.
Hassan, Omar
Kitzig, Ella
Müller, Ines
El-Bahrawy, Mona A.
von Karstedt, Silvia
Kulms, Dagmar
Liccardi, Gianmaria
Lemke, Johannes
Walczak, Henning
author_sort Montinaro, Antonella
collection PubMed
description Primary or acquired therapy resistance is a major obstacle to the effective treatment of cancer. Resistance to apoptosis has long been thought to contribute to therapy resistance. We show here that recombinant TRAIL and CDK9 inhibition cooperate in killing cells derived from a broad range of cancers, importantly without inducing detectable adverse events. Remarkably, the combination of TRAIL with CDK9 inhibition was also highly effective on cancers resistant to both, standard-of-care chemotherapy and various targeted therapeutic approaches. Dynamic BH3 profiling revealed that, mechanistically, combining TRAIL with CDK9 inhibition induced a drastic increase in the mitochondrial priming of cancer cells. Intriguingly, this increase occurred irrespective of whether the cancer cells were sensitive or resistant to chemo- or targeted therapy. We conclude that this pro-apoptotic combination therapy has the potential to serve as a highly effective new treatment option for a variety of different cancers. Notably, this includes cancers that are resistant to currently available treatment modalities.
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spelling pubmed-89016602022-03-22 Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers Montinaro, Antonella Areso Zubiaur, Itziar Saggau, Julia Kretz, Anna-Laura Ferreira, Rute M. M. Hassan, Omar Kitzig, Ella Müller, Ines El-Bahrawy, Mona A. von Karstedt, Silvia Kulms, Dagmar Liccardi, Gianmaria Lemke, Johannes Walczak, Henning Cell Death Differ Article Primary or acquired therapy resistance is a major obstacle to the effective treatment of cancer. Resistance to apoptosis has long been thought to contribute to therapy resistance. We show here that recombinant TRAIL and CDK9 inhibition cooperate in killing cells derived from a broad range of cancers, importantly without inducing detectable adverse events. Remarkably, the combination of TRAIL with CDK9 inhibition was also highly effective on cancers resistant to both, standard-of-care chemotherapy and various targeted therapeutic approaches. Dynamic BH3 profiling revealed that, mechanistically, combining TRAIL with CDK9 inhibition induced a drastic increase in the mitochondrial priming of cancer cells. Intriguingly, this increase occurred irrespective of whether the cancer cells were sensitive or resistant to chemo- or targeted therapy. We conclude that this pro-apoptotic combination therapy has the potential to serve as a highly effective new treatment option for a variety of different cancers. Notably, this includes cancers that are resistant to currently available treatment modalities. Nature Publishing Group UK 2021-09-17 2022-03 /pmc/articles/PMC8901660/ /pubmed/34535764 http://dx.doi.org/10.1038/s41418-021-00869-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access 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 http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Montinaro, Antonella
Areso Zubiaur, Itziar
Saggau, Julia
Kretz, Anna-Laura
Ferreira, Rute M. M.
Hassan, Omar
Kitzig, Ella
Müller, Ines
El-Bahrawy, Mona A.
von Karstedt, Silvia
Kulms, Dagmar
Liccardi, Gianmaria
Lemke, Johannes
Walczak, Henning
Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
title Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
title_full Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
title_fullStr Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
title_full_unstemmed Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
title_short Potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
title_sort potent pro-apoptotic combination therapy is highly effective in a broad range of cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901660/
https://www.ncbi.nlm.nih.gov/pubmed/34535764
http://dx.doi.org/10.1038/s41418-021-00869-x
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