The Amphiregulin-EGFR Axis Drives Fibroblast Activation to Promote Keloid Progression.

BACKGROUND

Keloids represent a prevalent form of pathological scarring, yet their treatment remains highly challenging in clinical practice. The pathogenesis of keloids remains incompletely understood.

OBJECTIVES

To investigate the function and mechanism of AREG in keloids.

METHODS

We performed transcriptomic profiling of keloid fibroblasts (KFs) and normal fibroblasts (NFs). Keloid skin explants and keloid-bearing nude mice were used to explore the roles of AREG in keloids.

RESULTS

AREG was upregulated in keloids and associated with disease severity. In vitro, recombinant AREG promoted proliferation, migration, and extracellular matrix (ECM) production in KFs. We further demonstrated that AREG signalling mediates keloid fibroblast activation through EGFR. In addition, we revealed that the MAPK signalling pathway functions as a key downstream effector of the AREG-EGFR axis. As an EGFR antagonist, gefitinib effectively reduced ECM component deposition in both keloid skin explants and a nude mouse xenograft model.

CONCLUSIONS

These results not only highlight the role of AREG in driving keloid progression but also point to the translational relevance of gefitinib as a viable therapeutic candidate for keloids.