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Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis

Copper levels are known to be elevated in inflamed and malignant tissues. But the mechanism underlying this selective enrichment has been elusive. In this study, we report a axis by which inflammatory cytokines, such as IL-17, drive cellular copper uptake via the induction of a metalloreductase, STE...

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Autores principales: Liao, Yun, Zhao, Junjie, Bulek, Katarzyna, Tang, Fangqiang, Chen, Xing, Cai, Gang, Jia, Shang, Fox, Paul L., Huang, Emina, Pizarro, Theresa T., Kalady, Matthew F., Jackson, Mark W., Bao, Shideng, Sen, Ganes C., Stark, George R., Chang, Christopher J., Li, Xiaoxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021685/
https://www.ncbi.nlm.nih.gov/pubmed/32060280
http://dx.doi.org/10.1038/s41467-020-14698-y
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author Liao, Yun
Zhao, Junjie
Bulek, Katarzyna
Tang, Fangqiang
Chen, Xing
Cai, Gang
Jia, Shang
Fox, Paul L.
Huang, Emina
Pizarro, Theresa T.
Kalady, Matthew F.
Jackson, Mark W.
Bao, Shideng
Sen, Ganes C.
Stark, George R.
Chang, Christopher J.
Li, Xiaoxia
author_facet Liao, Yun
Zhao, Junjie
Bulek, Katarzyna
Tang, Fangqiang
Chen, Xing
Cai, Gang
Jia, Shang
Fox, Paul L.
Huang, Emina
Pizarro, Theresa T.
Kalady, Matthew F.
Jackson, Mark W.
Bao, Shideng
Sen, Ganes C.
Stark, George R.
Chang, Christopher J.
Li, Xiaoxia
author_sort Liao, Yun
collection PubMed
description Copper levels are known to be elevated in inflamed and malignant tissues. But the mechanism underlying this selective enrichment has been elusive. In this study, we report a axis by which inflammatory cytokines, such as IL-17, drive cellular copper uptake via the induction of a metalloreductase, STEAP4. IL-17-induced elevated intracellular copper level leads to the activation of an E3-ligase, XIAP, which potentiates IL-17-induced NFκB activation and suppresses the caspase 3 activity. Importantly, this IL-17-induced STEAP4-dependent cellular copper uptake is critical for colon tumor formation in a murine model of colitis-associated tumorigenesis and STEAP4 expression correlates with IL-17 level and XIAP activation in human colon cancer. In summary, this study reveals a IL-17-STEAP4-XIAP axis through which the inflammatory response induces copper uptake, promoting colon tumorigenesis.
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spelling pubmed-70216852020-02-21 Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis Liao, Yun Zhao, Junjie Bulek, Katarzyna Tang, Fangqiang Chen, Xing Cai, Gang Jia, Shang Fox, Paul L. Huang, Emina Pizarro, Theresa T. Kalady, Matthew F. Jackson, Mark W. Bao, Shideng Sen, Ganes C. Stark, George R. Chang, Christopher J. Li, Xiaoxia Nat Commun Article Copper levels are known to be elevated in inflamed and malignant tissues. But the mechanism underlying this selective enrichment has been elusive. In this study, we report a axis by which inflammatory cytokines, such as IL-17, drive cellular copper uptake via the induction of a metalloreductase, STEAP4. IL-17-induced elevated intracellular copper level leads to the activation of an E3-ligase, XIAP, which potentiates IL-17-induced NFκB activation and suppresses the caspase 3 activity. Importantly, this IL-17-induced STEAP4-dependent cellular copper uptake is critical for colon tumor formation in a murine model of colitis-associated tumorigenesis and STEAP4 expression correlates with IL-17 level and XIAP activation in human colon cancer. In summary, this study reveals a IL-17-STEAP4-XIAP axis through which the inflammatory response induces copper uptake, promoting colon tumorigenesis. Nature Publishing Group UK 2020-02-14 /pmc/articles/PMC7021685/ /pubmed/32060280 http://dx.doi.org/10.1038/s41467-020-14698-y 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
Liao, Yun
Zhao, Junjie
Bulek, Katarzyna
Tang, Fangqiang
Chen, Xing
Cai, Gang
Jia, Shang
Fox, Paul L.
Huang, Emina
Pizarro, Theresa T.
Kalady, Matthew F.
Jackson, Mark W.
Bao, Shideng
Sen, Ganes C.
Stark, George R.
Chang, Christopher J.
Li, Xiaoxia
Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis
title Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis
title_full Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis
title_fullStr Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis
title_full_unstemmed Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis
title_short Inflammation mobilizes copper metabolism to promote colon tumorigenesis via an IL-17-STEAP4-XIAP axis
title_sort inflammation mobilizes copper metabolism to promote colon tumorigenesis via an il-17-steap4-xiap axis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021685/
https://www.ncbi.nlm.nih.gov/pubmed/32060280
http://dx.doi.org/10.1038/s41467-020-14698-y
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