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Protein driver of cutaneous radiotherapy damage identified
DKK3 in keratinocytes orchestrates radiation-induced skin hyperplasia, dermatitis, and fibrosis. Radiation-induced reactive oxygen species (ROS) increase DKK3 expression in keratinocytes, which subsequently activates canonical Wnt signaling through autocrine TGF-β signaling. Elevated DKK3 levels in keratinocytes drive hyperproliferation and hyperplasia, promoting the polarization of macrophages toward a profibrotic phenotype. These polarized macrophages, in turn, upregulate..
John Evans
Feb 62 min read
Disturbed microbiome a risk factor for severe radiodermatitis
Findings from a pilot study suggest the skin microbiome plays an important role in the risk of radiodermatitis associated with cancer...
John Evans
Feb 2, 20243 min read
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