Heterogeneity of epithelial-mesenchymal transition and CD26 expression in hypertrophic scars and keloids
GONG Wanru,
LIU Mengchang,
LIU Xingke,
XIE Defu,
YAN Hong
Affiliations
GONG Wanru
Department of Plastic and Burn Surgery, National Key Clinical Construction Specialty, Wound Repair and Regeneration Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China
LIU Mengchang
Department of Plastic and Burn Surgery, National Key Clinical Construction Specialty, Wound Repair and Regeneration Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China
LIU Xingke
Department of Plastic and Burn Surgery, National Key Clinical Construction Specialty, Wound Repair and Regeneration Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China
XIE Defu
Department of Plastic and Burn Surgery, National Key Clinical Construction Specialty, Wound Repair and Regeneration Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China
YAN Hong
Department of Plastic and Burn Surgery, National Key Clinical Construction Specialty, Wound Repair and Regeneration Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China
Objective To investigate the histological differences and expression of E-cadherin, Vimentin, matrix metalloprotein-9 (MMP-9), TNF-α, dipeptidyl-peptidase 4 (DPP4, also called CD26) in the margin and center of hypertrophic scar, superficial dilated keloid and normal skin. Methods Ten patients with keloid and another 10 with hypertrophic scar undergoing excision surgery in our hospital from October 2020 to August 2021 were included, and 8 cases requiring partial normal skin resection were also recruited. The resected tissues were collected, the tissue morphology was observed with HE staining, and the expression levels of E-cadherin, Vimentin, MMP-9, TNF-α and CD26 were detected by immunohistochemical staining and Western blotting. Results The E-cadherin expression in the epidermis of both keloid and hypertrophic scar was significantly lower than that of normal skin (P 0.05). By contrast, the expression levels of Vimentin, MMP-9, TNF-α and CD26 in the epidermis of both keloid and hypertrophic scar were remarkably enhanced when compared with those of normal skin (P 0.05). Conclusion The differences in epithelial-to-mesenchymal transition (EMT) and expression of relevant biomarkers within individual scars may be one of the reasons for the diversity of clinical features between hypertrophic scar and keloid, in which TNF-α and CD26 may be the key factors.
