Hair Eruption Initiates and Commensal Skin Microbiota Aggravate Adverse Events of Anti-EGFR Therapy

    December 2019 in “ Science Translational Medicine
    Jörg Klufa, Thomas Bauer, Buck Hanson, Craig W. Herbold, Philipp Starkl, Beate M. Lichtenberger, Dagmar Šrůtková, Daniel Schulz, Igor Vujic, Thomas Mohr, Klemens Rappersberger, Bernd Bodenmiller, Hana Kozáková, Sylvia Knapp, Alexander Loy, Maria Sibilia
    Studysummary This study found that EGFR-targeted cancer therapy can cause skin toxicities by disrupting epidermal signaling, allowing microbiota invasion and inflammation, but identified a potential treatment approach using FGF7 or SOS expression to restore barrier integrity.
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    The study by Klufa et al. explored the adverse skin effects of anti-EGFR therapy, commonly used in cancer treatment. They found that inhibiting EGFR disrupts the ability of skin stem cells to maintain a protective barrier during hair eruption, allowing microorganisms to invade and cause inflammation similar to atopic dermatitis. This process involves a TH2-dominated immune response and can lead to chronic folliculitis. The researchers identified that restoring epidermal ERK signaling, through methods like FGF7 treatment, could mitigate these skin issues without directly reactivating EGFR. This discovery provided a potential therapeutic approach to manage the skin toxicities associated with EGFR-targeted cancer therapies.
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