• Zi Li, Wenhui Zhang, and Heting Zhang.
• Department of Orthopedics & Plastic Surgery, The Sixth Hospital of Wuhan, Affiliated Hospital of Jianghan University, Wuhan 430015, Hubei, China.
• Burns. 2023 Dec 1; 49 (8): 200720172007-2017.

BackgroundAberrant biofunction of circular RNAs (circRNAs) is potently implicated in keloid formation. However, their roles have been underinvestigated. Recent evidence has demonstrated the pro-tumor role of circ_0000129 in cancers, and yet its role in keloid remains elusive.MethodsRT-qPCR analysis and or western blotting of miR-485-3p, circ_0000129, and SGMS2 in keloid tissues and keloid fibroblasts was implemented. CCK8, EdU, scratch wound healing, and Transwell migration assays were perfomed to determine the keloid fibroblast proliferation and migration. Luciferase reporter and RIP assays were adopted to analyze the interaction among circ_0000129, miR-485-3p and SGMS2.ResultsIn keloid tissues and keloid fibroblasts, circ_0000129 and SGMS2 were amplified, although miR-485-3p expression was downregulated. Furthermore, siRNAs-targeting endogenous circ_0000129 resulted in proliferation and migration defect of keloid fibroblasts. MiR-485-3p was simultaneously recognized by circ_0000129 and SGMS2 3'UTR. Rescued functional assays also illustrated that miR-485-3p loss was beneficial to the proliferation and migration of keloid fibroblasts, and these promoting changes were nullified by accompanied silence circ_0000129 or SGMS2.ConclusionCirc_0000129 sponges miR-485-3p and releases expression of SGMS2 from the miR-485-3p suppression, promoting migration and proliferation of keloid fibroblasts, suggesting targeting circ_0000129/miR-485-3p/SGMS2 might be a promising strategy against keloid fibroblasts.Availability Of Data And MaterialAll data generated or analyzed during this study are included in this article.Copyright © 2023 Elsevier Ltd and International Society of Burns Injuries. All rights reserved.

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