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Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities

Utilizing oxidative stress has recently been regarded as a potential strategy for tumor therapy. The NUAK family SNF1-like kinase 1 (NUAK1) is a critical component of the antioxidant defense system and is necessary for the survival of tumors. Therefore, NUAK1 is considered an attractive therapeutic...

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Autores principales: Chen, Yiran, Xie, Xiaoling, Wang, Chunsheng, Hu, Yuxing, Zhang, Honghao, Zhang, Lenghe, Tu, Sanfang, He, Yanjie, Li, Yuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463258/
https://www.ncbi.nlm.nih.gov/pubmed/32873786
http://dx.doi.org/10.1038/s41419-020-02885-0
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author Chen, Yiran
Xie, Xiaoling
Wang, Chunsheng
Hu, Yuxing
Zhang, Honghao
Zhang, Lenghe
Tu, Sanfang
He, Yanjie
Li, Yuhua
author_facet Chen, Yiran
Xie, Xiaoling
Wang, Chunsheng
Hu, Yuxing
Zhang, Honghao
Zhang, Lenghe
Tu, Sanfang
He, Yanjie
Li, Yuhua
author_sort Chen, Yiran
collection PubMed
description Utilizing oxidative stress has recently been regarded as a potential strategy for tumor therapy. The NUAK family SNF1-like kinase 1 (NUAK1) is a critical component of the antioxidant defense system and is necessary for the survival of tumors. Therefore, NUAK1 is considered an attractive therapeutic target in cancer. However, antioxidant therapy induced elevated ROS levels to activate the Unc-51-like kinase 1 (ULK1) pathway to promote protective autophagy and ULK1-dependent mitophagy. Thus, the combined inhibition of NUAK1 and ULK1 showed a strong synergistic effect in different tumor types. Herein, the potential antitumor activities of a dual NUAK1/ULK1 inhibitor MRT68921 were evaluated in both tumor cell lines and animal models. MRT68921 significantly kills tumor cells by breaking the balance of oxidative stress signals. These results highlight the potential of MRT68921 as an effective agent for tumor therapy.
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spelling pubmed-74632582020-09-11 Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities Chen, Yiran Xie, Xiaoling Wang, Chunsheng Hu, Yuxing Zhang, Honghao Zhang, Lenghe Tu, Sanfang He, Yanjie Li, Yuhua Cell Death Dis Article Utilizing oxidative stress has recently been regarded as a potential strategy for tumor therapy. The NUAK family SNF1-like kinase 1 (NUAK1) is a critical component of the antioxidant defense system and is necessary for the survival of tumors. Therefore, NUAK1 is considered an attractive therapeutic target in cancer. However, antioxidant therapy induced elevated ROS levels to activate the Unc-51-like kinase 1 (ULK1) pathway to promote protective autophagy and ULK1-dependent mitophagy. Thus, the combined inhibition of NUAK1 and ULK1 showed a strong synergistic effect in different tumor types. Herein, the potential antitumor activities of a dual NUAK1/ULK1 inhibitor MRT68921 were evaluated in both tumor cell lines and animal models. MRT68921 significantly kills tumor cells by breaking the balance of oxidative stress signals. These results highlight the potential of MRT68921 as an effective agent for tumor therapy. Nature Publishing Group UK 2020-09-01 /pmc/articles/PMC7463258/ /pubmed/32873786 http://dx.doi.org/10.1038/s41419-020-02885-0 Text en © The Author(s) 2020 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
Chen, Yiran
Xie, Xiaoling
Wang, Chunsheng
Hu, Yuxing
Zhang, Honghao
Zhang, Lenghe
Tu, Sanfang
He, Yanjie
Li, Yuhua
Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities
title Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities
title_full Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities
title_fullStr Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities
title_full_unstemmed Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities
title_short Dual targeting of NUAK1 and ULK1 using the multitargeted inhibitor MRT68921 exerts potent antitumor activities
title_sort dual targeting of nuak1 and ulk1 using the multitargeted inhibitor mrt68921 exerts potent antitumor activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463258/
https://www.ncbi.nlm.nih.gov/pubmed/32873786
http://dx.doi.org/10.1038/s41419-020-02885-0
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