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NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2

Background: Metastasis is the most common cause of lethal outcome in various types of cancers. Although the cell proliferation related metabolism rewiring has been well characterized, less is known about the association of metabolic changes with tumor metastasis. Herein, we demonstrate that metastat...

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Autores principales: Ding, Mingchao, Bu, Xin, Li, Zhehao, Xu, Haokun, Feng, Lin, Hu, Junbi, Wei, Xinxin, Gao, Jiwei, Tao, Yanyan, Cai, Bolei, Liu, Yanpu, Qu, Xuan, Shen, Liangliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645990/
https://www.ncbi.nlm.nih.gov/pubmed/33162818
http://dx.doi.org/10.7150/ijbs.48066
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author Ding, Mingchao
Bu, Xin
Li, Zhehao
Xu, Haokun
Feng, Lin
Hu, Junbi
Wei, Xinxin
Gao, Jiwei
Tao, Yanyan
Cai, Bolei
Liu, Yanpu
Qu, Xuan
Shen, Liangliang
author_facet Ding, Mingchao
Bu, Xin
Li, Zhehao
Xu, Haokun
Feng, Lin
Hu, Junbi
Wei, Xinxin
Gao, Jiwei
Tao, Yanyan
Cai, Bolei
Liu, Yanpu
Qu, Xuan
Shen, Liangliang
author_sort Ding, Mingchao
collection PubMed
description Background: Metastasis is the most common cause of lethal outcome in various types of cancers. Although the cell proliferation related metabolism rewiring has been well characterized, less is known about the association of metabolic changes with tumor metastasis. Herein, we demonstrate that metastatic tumor obtained a mesenchymal phenotype, which is obtained by the loss of tumor suppressor NDRG2 triggered metabolic switch to glutamine metabolism. Methods: mRNA-seq and gene expression profile analysis were performed to define the differential gene expressions in primary MEC1 and metastatic MC3 cells and the downstream pathways of NDRG2. NDRG2 regulation of Fbw7-dependent c-Myc stability were determined by immunoprecipitation and protein half-life assay. Luciferase reporter and ChIP assays were used to determine the roles of Akt and c-Myc in mediating NDRG2-dependent regulation of ASCT2 in in both tumor and NDRG2-knockout MEF cells. Finally, the effect of the NDRG2/Akt/c-Myc/ASCT2 signaling on glutaminolysis and tumor metastasis were evaluated by functional experiments and clinical samples. Results: Based on the gene expression profile analysis, we identified metastatic tumor cells acquired the mesenchymal-like characteristics and displayed the increased dependency on glutamine utilization. Further, the gain of NDRG2 function blocked epithelial-mesenchymal transition (EMT) and glutaminolysis, potentially through suppression of glutamine transporter ASCT2 expression. The ASCT2 restoration reversed NDRG2 inhibitory effect on EMT program and tumor metastasis. Mechanistic study indicates that NDRG2 promoted Fbw7-dependent c-Myc degradation by inhibiting Akt activation, and subsequently decreased c-Myc-mediated ASCT2 transcription, in both tumor and NDRG2-knockout MEF cells. Supporting the biological significance, the reciprocal relationship between NDRG2 and ASCT2 were observed in multiple types of tumor tissues, and associated with tumor malignancy. Conclusions: NDRG2-dependent repression of ASCT2 presumably is the predominant route by which NDRG2 rewires glutaminolysis and blocks metastatic tumor survival. Targeting glutaminolytic pathway may provide a new strategy for the treatment of metastatic tumors.
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spelling pubmed-76459902020-11-06 NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2 Ding, Mingchao Bu, Xin Li, Zhehao Xu, Haokun Feng, Lin Hu, Junbi Wei, Xinxin Gao, Jiwei Tao, Yanyan Cai, Bolei Liu, Yanpu Qu, Xuan Shen, Liangliang Int J Biol Sci Research Paper Background: Metastasis is the most common cause of lethal outcome in various types of cancers. Although the cell proliferation related metabolism rewiring has been well characterized, less is known about the association of metabolic changes with tumor metastasis. Herein, we demonstrate that metastatic tumor obtained a mesenchymal phenotype, which is obtained by the loss of tumor suppressor NDRG2 triggered metabolic switch to glutamine metabolism. Methods: mRNA-seq and gene expression profile analysis were performed to define the differential gene expressions in primary MEC1 and metastatic MC3 cells and the downstream pathways of NDRG2. NDRG2 regulation of Fbw7-dependent c-Myc stability were determined by immunoprecipitation and protein half-life assay. Luciferase reporter and ChIP assays were used to determine the roles of Akt and c-Myc in mediating NDRG2-dependent regulation of ASCT2 in in both tumor and NDRG2-knockout MEF cells. Finally, the effect of the NDRG2/Akt/c-Myc/ASCT2 signaling on glutaminolysis and tumor metastasis were evaluated by functional experiments and clinical samples. Results: Based on the gene expression profile analysis, we identified metastatic tumor cells acquired the mesenchymal-like characteristics and displayed the increased dependency on glutamine utilization. Further, the gain of NDRG2 function blocked epithelial-mesenchymal transition (EMT) and glutaminolysis, potentially through suppression of glutamine transporter ASCT2 expression. The ASCT2 restoration reversed NDRG2 inhibitory effect on EMT program and tumor metastasis. Mechanistic study indicates that NDRG2 promoted Fbw7-dependent c-Myc degradation by inhibiting Akt activation, and subsequently decreased c-Myc-mediated ASCT2 transcription, in both tumor and NDRG2-knockout MEF cells. Supporting the biological significance, the reciprocal relationship between NDRG2 and ASCT2 were observed in multiple types of tumor tissues, and associated with tumor malignancy. Conclusions: NDRG2-dependent repression of ASCT2 presumably is the predominant route by which NDRG2 rewires glutaminolysis and blocks metastatic tumor survival. Targeting glutaminolytic pathway may provide a new strategy for the treatment of metastatic tumors. Ivyspring International Publisher 2020-10-16 /pmc/articles/PMC7645990/ /pubmed/33162818 http://dx.doi.org/10.7150/ijbs.48066 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Ding, Mingchao
Bu, Xin
Li, Zhehao
Xu, Haokun
Feng, Lin
Hu, Junbi
Wei, Xinxin
Gao, Jiwei
Tao, Yanyan
Cai, Bolei
Liu, Yanpu
Qu, Xuan
Shen, Liangliang
NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2
title NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2
title_full NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2
title_fullStr NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2
title_full_unstemmed NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2
title_short NDRG2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of ASCT2
title_sort ndrg2 ablation reprograms metastatic cancer cells towards glutamine dependence via the induction of asct2
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645990/
https://www.ncbi.nlm.nih.gov/pubmed/33162818
http://dx.doi.org/10.7150/ijbs.48066
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