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

Yun Liao(Sichuan University), Junjie Zhao(Cleveland Clinic Lerner College of Medicine), Katarzyna Bulek(Jagiellonian University), Fangqiang Tang(Cleveland Clinic Lerner College of Medicine), Xing Chen(Cleveland Clinic Lerner College of Medicine), Gang Cai(Cleveland Clinic Lerner College of Medicine), Shang Jia(University of California, Berkeley), Paul L. Fox(Cleveland Clinic Lerner College of Medicine), Emina H. Huang(Cleveland Clinic Lerner College of Medicine), Theresa T. Pizarro(Case Western Reserve University), Matthew F. Kalady(Cleveland Clinic Lerner College of Medicine), Mark W. Jackson(Case Western Reserve University), Shideng Bao(Cleveland Clinic Lerner College of Medicine), Ganes C. Sen(Cleveland Clinic Lerner College of Medicine), George R. Stark(Cleveland Clinic Lerner College of Medicine), Christopher J. Chang(Howard Hughes Medical Institute), Xiaoxia Li(Cleveland Clinic Lerner College of Medicine)
Nature Communications
February 14, 2020
Cited by 239Open Access
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Abstract

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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