Prof. Dr. Dr. Thomas Bieber
Department of Dermatology & Allergology
direktion.dermatologie@ukbonn.de View member: Prof. Dr. Dr. Thomas Bieber
Oncotarget
OBJECTIVE: Epidermal growth factor receptor inhibitors (EGFRI) are used as targeted cancer therapy. On average 70% of patients treated with EGFRIs suffer from skin toxicity. Studies showed a correlation between overall survival and the appearance of a skin rash, which is used as a biomarker for therapy efficacy. Micro RNAs (miRNA) as tumor or resistance biomarkers for cancer therapy are also highly investigated. In our study, we searched for associations of miRNA expression profiles in serum, with the severity of skin rash, in order to identify tentative therapy predictive biomarkers.
MATERIALS AND METHODS: Five candidate miRNAs were selected, based on an earlier next-generation-sequencing-experiment and after literature search. MiR-21, miR-31, miR-17, miR-106b and miR-520e were investigated in serum samples from patients ( = 254) treated with EGFRI. The quantitative expression of miRNA was tested for association with the occurrence/severity of the rash.
RESULTS: In our cohort of patients treated with EGFR inhibiting monoclonal antibodies, miR-21 and miR-520e serum concentrations were negatively correlated with severity of skin rash (-value 0.000582 and 1.53e-07 linear-trend-test) whereas for miR-31, a positive correlation was observed (-value 9.01e-06 linear-trend-test).
CONCLUSIONS: This suggests that miR-21, miR-31 and miR-520e expression might be a treatment dependent marker for EGFRI induced skin rash.
Copyright: © 2021 Kemski et al.
PMID: 34012511
Department of Dermatology & Allergology
direktion.dermatologie@ukbonn.de View member: Prof. Dr. Dr. Thomas Bieber