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CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer

Tumor cells, including cancer stem cells (CSCs) resistant to radio- and chemotherapy, must enhance metabolism to meet the extra energy demands to repair and survive such genotoxic conditions. However, such stress-induced adaptive metabolic alterations, especially in cancer cells that survive radioth...

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Autores principales: Han, Shujun, Wei, Ryan, Zhang, Xiaodi, Jiang, Nian, Fan, Ming, Huang, Jie Hunter, Xie, Bowen, Zhang, Lu, Miao, Weili, Butler, Ashley Chen-Ping, Coleman, Matthew A., Vaughan, Andrew T., Wang, Yinsheng, Chen, Hong-Wu, Liu, Jiankang, Li, Jian Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873486/
https://www.ncbi.nlm.nih.gov/pubmed/31803610
http://dx.doi.org/10.3389/fonc.2019.01201
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author Han, Shujun
Wei, Ryan
Zhang, Xiaodi
Jiang, Nian
Fan, Ming
Huang, Jie Hunter
Xie, Bowen
Zhang, Lu
Miao, Weili
Butler, Ashley Chen-Ping
Coleman, Matthew A.
Vaughan, Andrew T.
Wang, Yinsheng
Chen, Hong-Wu
Liu, Jiankang
Li, Jian Jian
author_facet Han, Shujun
Wei, Ryan
Zhang, Xiaodi
Jiang, Nian
Fan, Ming
Huang, Jie Hunter
Xie, Bowen
Zhang, Lu
Miao, Weili
Butler, Ashley Chen-Ping
Coleman, Matthew A.
Vaughan, Andrew T.
Wang, Yinsheng
Chen, Hong-Wu
Liu, Jiankang
Li, Jian Jian
author_sort Han, Shujun
collection PubMed
description Tumor cells, including cancer stem cells (CSCs) resistant to radio- and chemotherapy, must enhance metabolism to meet the extra energy demands to repair and survive such genotoxic conditions. However, such stress-induced adaptive metabolic alterations, especially in cancer cells that survive radiotherapy, remain unresolved. In this study, we found that CPT1 (Carnitine palmitoyl transferase I) and CPT2 (Carnitine palmitoyl transferase II), a pair of rate-limiting enzymes for mitochondrial fatty acid transportation, play a critical role in increasing fatty acid oxidation (FAO) required for the cellular fuel demands in radioresistant breast cancer cells (RBCs) and radiation-derived breast cancer stem cells (RD-BCSCs). Enhanced CPT1A/CPT2 expression was detected in the recurrent human breast cancers and associated with a worse prognosis in breast cancer patients. Blocking FAO via a FAO inhibitor or by CRISPR-mediated CPT1A/CPT2 gene deficiency inhibited radiation-induced ERK activation and aggressive growth and radioresistance of RBCs and RD-BCSCs. These results revealed that switching to FAO contributes to radiation-induced mitochondrial energy metabolism, and CPT1A/CPT2 is a potential metabolic target in cancer radiotherapy.
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spelling pubmed-68734862019-12-04 CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer Han, Shujun Wei, Ryan Zhang, Xiaodi Jiang, Nian Fan, Ming Huang, Jie Hunter Xie, Bowen Zhang, Lu Miao, Weili Butler, Ashley Chen-Ping Coleman, Matthew A. Vaughan, Andrew T. Wang, Yinsheng Chen, Hong-Wu Liu, Jiankang Li, Jian Jian Front Oncol Oncology Tumor cells, including cancer stem cells (CSCs) resistant to radio- and chemotherapy, must enhance metabolism to meet the extra energy demands to repair and survive such genotoxic conditions. However, such stress-induced adaptive metabolic alterations, especially in cancer cells that survive radiotherapy, remain unresolved. In this study, we found that CPT1 (Carnitine palmitoyl transferase I) and CPT2 (Carnitine palmitoyl transferase II), a pair of rate-limiting enzymes for mitochondrial fatty acid transportation, play a critical role in increasing fatty acid oxidation (FAO) required for the cellular fuel demands in radioresistant breast cancer cells (RBCs) and radiation-derived breast cancer stem cells (RD-BCSCs). Enhanced CPT1A/CPT2 expression was detected in the recurrent human breast cancers and associated with a worse prognosis in breast cancer patients. Blocking FAO via a FAO inhibitor or by CRISPR-mediated CPT1A/CPT2 gene deficiency inhibited radiation-induced ERK activation and aggressive growth and radioresistance of RBCs and RD-BCSCs. These results revealed that switching to FAO contributes to radiation-induced mitochondrial energy metabolism, and CPT1A/CPT2 is a potential metabolic target in cancer radiotherapy. Frontiers Media S.A. 2019-11-15 /pmc/articles/PMC6873486/ /pubmed/31803610 http://dx.doi.org/10.3389/fonc.2019.01201 Text en Copyright © 2019 Han, Wei, Zhang, Jiang, Fan, Huang, Xie, Zhang, Miao, Butler, Coleman, Vaughan, Wang, Chen, Liu and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Han, Shujun
Wei, Ryan
Zhang, Xiaodi
Jiang, Nian
Fan, Ming
Huang, Jie Hunter
Xie, Bowen
Zhang, Lu
Miao, Weili
Butler, Ashley Chen-Ping
Coleman, Matthew A.
Vaughan, Andrew T.
Wang, Yinsheng
Chen, Hong-Wu
Liu, Jiankang
Li, Jian Jian
CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer
title CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer
title_full CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer
title_fullStr CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer
title_full_unstemmed CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer
title_short CPT1A/2-Mediated FAO Enhancement—A Metabolic Target in Radioresistant Breast Cancer
title_sort cpt1a/2-mediated fao enhancement—a metabolic target in radioresistant breast cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873486/
https://www.ncbi.nlm.nih.gov/pubmed/31803610
http://dx.doi.org/10.3389/fonc.2019.01201
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