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AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation

BACKGROUND: Medulloblastoma (MB) is one of the most common malignant pediatric brain tumors. Metastasis and relapse are the leading causes of death in MB patients. The initiation of the SHH subgroup of MB (SHH-MB) is due to the aberrant activation of Sonic Hedgehog (Shh) signaling. However, the mech...

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Autores principales: Cai, Jing, Wang, Yue, Wang, Xinfa, Ai, Zihe, Li, Tianyuan, Pu, Xiaohong, Yang, Xin, Yao, Yixing, He, Junping, Cheng, Steven Y., Yu, Tingting, Liu, Chen, Yue, Shen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867863/
https://www.ncbi.nlm.nih.gov/pubmed/36683064
http://dx.doi.org/10.1186/s13578-023-00963-2
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author Cai, Jing
Wang, Yue
Wang, Xinfa
Ai, Zihe
Li, Tianyuan
Pu, Xiaohong
Yang, Xin
Yao, Yixing
He, Junping
Cheng, Steven Y.
Yu, Tingting
Liu, Chen
Yue, Shen
author_facet Cai, Jing
Wang, Yue
Wang, Xinfa
Ai, Zihe
Li, Tianyuan
Pu, Xiaohong
Yang, Xin
Yao, Yixing
He, Junping
Cheng, Steven Y.
Yu, Tingting
Liu, Chen
Yue, Shen
author_sort Cai, Jing
collection PubMed
description BACKGROUND: Medulloblastoma (MB) is one of the most common malignant pediatric brain tumors. Metastasis and relapse are the leading causes of death in MB patients. The initiation of the SHH subgroup of MB (SHH-MB) is due to the aberrant activation of Sonic Hedgehog (Shh) signaling. However, the mechanisms for its metastasis are still unknown. RESULTS: AMP-dependent protein kinase (AMPK) restrains the activation of Shh signaling pathway, thereby impeding the proliferation of SHH-MB cells. More importantly, AMPK also hinders the growth and metastasis of SHH-MB cells by regulating NF-κB signaling pathway. Furthermore, Vismodegib and TPCA-1, which block the Shh and NF-κB pathways, respectively, synergistically restrained the growth, migration, and invasion of SHH-MB cells. CONCLUSIONS: This work demonstrates that AMPK functions through two signaling pathways, SHH-GLI1 and NF-κB. AMPK-NF-κB axis is a potential target for molecular therapy of SHH-MB, and the combinational blockade of NF-κB and Shh pathways confers synergy for SHH-MB therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-023-00963-2.
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spelling pubmed-98678632023-01-23 AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation Cai, Jing Wang, Yue Wang, Xinfa Ai, Zihe Li, Tianyuan Pu, Xiaohong Yang, Xin Yao, Yixing He, Junping Cheng, Steven Y. Yu, Tingting Liu, Chen Yue, Shen Cell Biosci Research BACKGROUND: Medulloblastoma (MB) is one of the most common malignant pediatric brain tumors. Metastasis and relapse are the leading causes of death in MB patients. The initiation of the SHH subgroup of MB (SHH-MB) is due to the aberrant activation of Sonic Hedgehog (Shh) signaling. However, the mechanisms for its metastasis are still unknown. RESULTS: AMP-dependent protein kinase (AMPK) restrains the activation of Shh signaling pathway, thereby impeding the proliferation of SHH-MB cells. More importantly, AMPK also hinders the growth and metastasis of SHH-MB cells by regulating NF-κB signaling pathway. Furthermore, Vismodegib and TPCA-1, which block the Shh and NF-κB pathways, respectively, synergistically restrained the growth, migration, and invasion of SHH-MB cells. CONCLUSIONS: This work demonstrates that AMPK functions through two signaling pathways, SHH-GLI1 and NF-κB. AMPK-NF-κB axis is a potential target for molecular therapy of SHH-MB, and the combinational blockade of NF-κB and Shh pathways confers synergy for SHH-MB therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-023-00963-2. BioMed Central 2023-01-22 /pmc/articles/PMC9867863/ /pubmed/36683064 http://dx.doi.org/10.1186/s13578-023-00963-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cai, Jing
Wang, Yue
Wang, Xinfa
Ai, Zihe
Li, Tianyuan
Pu, Xiaohong
Yang, Xin
Yao, Yixing
He, Junping
Cheng, Steven Y.
Yu, Tingting
Liu, Chen
Yue, Shen
AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation
title AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation
title_full AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation
title_fullStr AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation
title_full_unstemmed AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation
title_short AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation
title_sort ampk attenuates shh subgroup medulloblastoma growth and metastasis by inhibiting nf-κb activation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867863/
https://www.ncbi.nlm.nih.gov/pubmed/36683064
http://dx.doi.org/10.1186/s13578-023-00963-2
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