Nature Communications · 2020 · 243 citations · 49 references
MedicineImmunologyOncologyCarcinogenesisCell SignalingInflammationCopper MetabolismCytokine BiologyCytokine SignalingGastrointestinal InflammationInflammation-associated CarcinogenesisInflammatory SignalingCellular Mineral UptakeColitis-associated Colorectal CancerColon Tumor PromotionCopper HomeostasisCopper SignalingCopper Uptake MechanismsInterleukin-17 PathwayMurine Models
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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