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A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma

Karonudib (TH1579) is a novel compound that exerts anti-tumor activities and has recently entered phase I clinical testing. The aim of this study was to conduct a pre-clinical trial in patient-derived xenografts to identify the possible biomarkers of response or resistance that could guide inclusion...

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Autores principales: Einarsdottir, Berglind O., Karlsson, Joakim, Söderberg, Elin M. V., Lindberg, Mattias F., Funck-Brentano, Elisa, Jespersen, Henrik, Brynjolfsson, Siggeir F., Olofsson Bagge, Roger, Carstam, Louise, Scobie, Martin, Koolmeister, Tobias, Wallner, Olof, Stierner, Ulrika, Berglund, Ulrika Warpman, Ny, Lars, Nilsson, Lisa M., Larsson, Erik, Helleday, Thomas, Nilsson, Jonas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057880/
https://www.ncbi.nlm.nih.gov/pubmed/30042422
http://dx.doi.org/10.1038/s41419-018-0865-6
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author Einarsdottir, Berglind O.
Karlsson, Joakim
Söderberg, Elin M. V.
Lindberg, Mattias F.
Funck-Brentano, Elisa
Jespersen, Henrik
Brynjolfsson, Siggeir F.
Olofsson Bagge, Roger
Carstam, Louise
Scobie, Martin
Koolmeister, Tobias
Wallner, Olof
Stierner, Ulrika
Berglund, Ulrika Warpman
Ny, Lars
Nilsson, Lisa M.
Larsson, Erik
Helleday, Thomas
Nilsson, Jonas A.
author_facet Einarsdottir, Berglind O.
Karlsson, Joakim
Söderberg, Elin M. V.
Lindberg, Mattias F.
Funck-Brentano, Elisa
Jespersen, Henrik
Brynjolfsson, Siggeir F.
Olofsson Bagge, Roger
Carstam, Louise
Scobie, Martin
Koolmeister, Tobias
Wallner, Olof
Stierner, Ulrika
Berglund, Ulrika Warpman
Ny, Lars
Nilsson, Lisa M.
Larsson, Erik
Helleday, Thomas
Nilsson, Jonas A.
author_sort Einarsdottir, Berglind O.
collection PubMed
description Karonudib (TH1579) is a novel compound that exerts anti-tumor activities and has recently entered phase I clinical testing. The aim of this study was to conduct a pre-clinical trial in patient-derived xenografts to identify the possible biomarkers of response or resistance that could guide inclusion of patients suffering from metastatic melanoma in phase II clinical trials. Patient-derived xenografts from 31 melanoma patients with metastatic disease were treated with karonudib or a vehicle for 18 days. Treatment responses were followed by measuring tumor sizes, and the models were categorized in the response groups. Tumors were harvested and processed for RNA sequencing and protein analysis. To investigate the effect of karonudib on T-cell-mediated anti-tumor activities, tumor-infiltrating T cells were injected in mice carrying autologous tumors and the mice treated with karonudib. We show that karonudib has heterogeneous anti-tumor effect on metastatic melanoma. Thus, based on the treatment responses, we could divide the 31 patient-derived xenografts in three treatment groups: progression group (32%), suppression group (42%), and regression group (26%). Furthermore, we show that karonudib has anti-tumor effect, irrespective of major melanoma driver mutations. Also, we identify high expression of ABCB1, which codes for p-gp pumps as a resistance biomarker. Finally, we show that karonudib treatment does not hamper T-cell-mediated anti-tumor responses. These findings can be used to guide future use of karonudib in clinical use with a potential approach as precision medicine.
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spelling pubmed-60578802018-07-27 A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma Einarsdottir, Berglind O. Karlsson, Joakim Söderberg, Elin M. V. Lindberg, Mattias F. Funck-Brentano, Elisa Jespersen, Henrik Brynjolfsson, Siggeir F. Olofsson Bagge, Roger Carstam, Louise Scobie, Martin Koolmeister, Tobias Wallner, Olof Stierner, Ulrika Berglund, Ulrika Warpman Ny, Lars Nilsson, Lisa M. Larsson, Erik Helleday, Thomas Nilsson, Jonas A. Cell Death Dis Article Karonudib (TH1579) is a novel compound that exerts anti-tumor activities and has recently entered phase I clinical testing. The aim of this study was to conduct a pre-clinical trial in patient-derived xenografts to identify the possible biomarkers of response or resistance that could guide inclusion of patients suffering from metastatic melanoma in phase II clinical trials. Patient-derived xenografts from 31 melanoma patients with metastatic disease were treated with karonudib or a vehicle for 18 days. Treatment responses were followed by measuring tumor sizes, and the models were categorized in the response groups. Tumors were harvested and processed for RNA sequencing and protein analysis. To investigate the effect of karonudib on T-cell-mediated anti-tumor activities, tumor-infiltrating T cells were injected in mice carrying autologous tumors and the mice treated with karonudib. We show that karonudib has heterogeneous anti-tumor effect on metastatic melanoma. Thus, based on the treatment responses, we could divide the 31 patient-derived xenografts in three treatment groups: progression group (32%), suppression group (42%), and regression group (26%). Furthermore, we show that karonudib has anti-tumor effect, irrespective of major melanoma driver mutations. Also, we identify high expression of ABCB1, which codes for p-gp pumps as a resistance biomarker. Finally, we show that karonudib treatment does not hamper T-cell-mediated anti-tumor responses. These findings can be used to guide future use of karonudib in clinical use with a potential approach as precision medicine. Nature Publishing Group UK 2018-07-24 /pmc/articles/PMC6057880/ /pubmed/30042422 http://dx.doi.org/10.1038/s41419-018-0865-6 Text en © The Author(s) 2018 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/.
spellingShingle Article
Einarsdottir, Berglind O.
Karlsson, Joakim
Söderberg, Elin M. V.
Lindberg, Mattias F.
Funck-Brentano, Elisa
Jespersen, Henrik
Brynjolfsson, Siggeir F.
Olofsson Bagge, Roger
Carstam, Louise
Scobie, Martin
Koolmeister, Tobias
Wallner, Olof
Stierner, Ulrika
Berglund, Ulrika Warpman
Ny, Lars
Nilsson, Lisa M.
Larsson, Erik
Helleday, Thomas
Nilsson, Jonas A.
A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
title A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
title_full A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
title_fullStr A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
title_full_unstemmed A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
title_short A patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
title_sort patient-derived xenograft pre-clinical trial reveals treatment responses and a resistance mechanism to karonudib in metastatic melanoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057880/
https://www.ncbi.nlm.nih.gov/pubmed/30042422
http://dx.doi.org/10.1038/s41419-018-0865-6
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