ATR inhibition enables complete tumour regression in ALK-driven NB mouse models

Effective therapeutic options are still needed in neuroblastoma treatment. Here, the authors, through a comprehensive proteomics analysis, identify ATR as a potential therapeutic target of neuroblastoma and demonstrate the efficacy of the ATR inhibitor BAY1895344 in combination with the ALK tyrosine...

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Autores principales: Joanna Szydzik, Dan E. Lind, Badrul Arefin, Yeshwant Kurhe, Ganesh Umapathy, Joachim Tetteh Siaw, Arne Claeys, Jonatan L. Gabre, Jimmy Van den Eynden, Bengt Hallberg, Ruth H. Palmer
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/06e9a92a8a164615981fa91b32e6d409
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spelling oai:doaj.org-article:06e9a92a8a164615981fa91b32e6d4092021-11-28T12:31:22ZATR inhibition enables complete tumour regression in ALK-driven NB mouse models10.1038/s41467-021-27057-22041-1723https://doaj.org/article/06e9a92a8a164615981fa91b32e6d4092021-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-27057-2https://doaj.org/toc/2041-1723Effective therapeutic options are still needed in neuroblastoma treatment. Here, the authors, through a comprehensive proteomics analysis, identify ATR as a potential therapeutic target of neuroblastoma and demonstrate the efficacy of the ATR inhibitor BAY1895344 in combination with the ALK tyrosine kinase inhibitor lorlatinib.Joanna SzydzikDan E. LindBadrul ArefinYeshwant KurheGanesh UmapathyJoachim Tetteh SiawArne ClaeysJonatan L. GabreJimmy Van den EyndenBengt HallbergRuth H. PalmerNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-18 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Joanna Szydzik
Dan E. Lind
Badrul Arefin
Yeshwant Kurhe
Ganesh Umapathy
Joachim Tetteh Siaw
Arne Claeys
Jonatan L. Gabre
Jimmy Van den Eynden
Bengt Hallberg
Ruth H. Palmer
ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
description Effective therapeutic options are still needed in neuroblastoma treatment. Here, the authors, through a comprehensive proteomics analysis, identify ATR as a potential therapeutic target of neuroblastoma and demonstrate the efficacy of the ATR inhibitor BAY1895344 in combination with the ALK tyrosine kinase inhibitor lorlatinib.
format article
author Joanna Szydzik
Dan E. Lind
Badrul Arefin
Yeshwant Kurhe
Ganesh Umapathy
Joachim Tetteh Siaw
Arne Claeys
Jonatan L. Gabre
Jimmy Van den Eynden
Bengt Hallberg
Ruth H. Palmer
author_facet Joanna Szydzik
Dan E. Lind
Badrul Arefin
Yeshwant Kurhe
Ganesh Umapathy
Joachim Tetteh Siaw
Arne Claeys
Jonatan L. Gabre
Jimmy Van den Eynden
Bengt Hallberg
Ruth H. Palmer
author_sort Joanna Szydzik
title ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
title_short ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
title_full ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
title_fullStr ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
title_full_unstemmed ATR inhibition enables complete tumour regression in ALK-driven NB mouse models
title_sort atr inhibition enables complete tumour regression in alk-driven nb mouse models
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/06e9a92a8a164615981fa91b32e6d409
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