Journal
JOURNAL OF DERMATOLOGICAL SCIENCE
Volume 75, Issue 2, Pages 94-99Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.jdermsci.2014.04.011
Keywords
Erlotinib; Gefitinib; Human beta-defensins
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Background: Epidermal growth factor receptor inhibitors (EGFRIs) have developed as one of the potential treatment options for various kinds of cancers. Although a variety of dermatological adverse reactions such as follicular acneiform eruptions is commonly encountered, the mechanism of the reactions remains unclear. Objectives: We investigated the effects of EGFRIs on the expression of human beta-defensins against staphylococci to study the pathomechanism of cutaneous adverse reactions caused by EGFRIs. Methods: We investigated the expressions of human beta-defensins 1, 2, and 3 (hBD1, 2, and 3) from staphylococci-stimulated normal human epidermal keratinocytes (NHEKs) cultured with or without the effects of two EGFRIs, gefitinib and erlotinib. We stimulated NHEKs with the supernatant of Staphylococcus aureus (S. aureus) and S. epidermidis and the live staphylococci. We measured hBDs in the culture supernatants of NHEKs by enzyme-linked immunosorbent assay (ELISA). Results: EGFRIs did not suppress the expressions of hBD1 and 3 induced by S. aureus. In contrast, EGFRIs suppressed the expressions of hBD2 and 3 induced by S. epidermidis. Conclusion: EGFRIs may cause cutaneous adverse effects through selectively perturbing innate immune responses induced by commensal and pathogenic bacteria. (C) 2014 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
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