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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7463258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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