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Chemical-Induced Skin Carcinogenesis Model Using Dimethylbenz[a]Anthracene and 12-O-Tetradecanoyl Phorbol-13-Acetate DMBA-TPA
Published on: December 19, 2019
Cancer Therapy-induced Dermatotoxicity as a Window to Understanding Skin Immunity
Yanek Jiménez-Andrade1, Jessica L Flesher1, Jin Mo Park1
1Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, 149 Thirteenth Street, Charlestown, MA 02129, USA.
Abstract:
Pruritus, rash, and various other forms of dermatotoxicity are the most frequent adverse events among patients with cancer receiving targeted molecular therapy and immunotherapy. Immune checkpoint inhibitors, macrophage-targeting agents, and epidermal growth factor receptor/MEK inhibitors not only exert antitumor effects but also interfere with molecular pathways essential for skin immune homeostasis. Studying cancer therapy-induced dermatotoxicity helps us identify molecular mechanisms governing skin immunity and deepen our understanding of human biology. This review summarizes new mechanistic insights emerging from the analysis of cutaneous adverse events and discusses knowledge gaps that remain to be closed by future research.
Insights
Cancer therapies like targeted molecular therapy and immunotherapy frequently cause skin problems. Studying these side effects reveals crucial insights into skin immunity and human biology.
Area of Science:
- Oncology
- Dermatology
- Immunology
Background:
- Targeted molecular therapies and immunotherapies are common cancer treatments.
- Dermatotoxicity, including rash and pruritus, is a frequent adverse event in patients undergoing these therapies.
- These therapies can disrupt molecular pathways vital for maintaining skin immune homeostasis.
Purpose of the Study:
- To review emerging mechanistic insights into cancer therapy-induced dermatotoxicity.
- To highlight the connection between cutaneous adverse events and skin immunity.
- To identify knowledge gaps for future research in this field.
Main Methods:
- Literature review of recent studies on cancer therapy-induced dermatotoxicity.
- Analysis of molecular mechanisms underlying skin immune homeostasis.
- Synthesis of findings on cutaneous adverse events from targeted therapies and immunotherapies.
Main Results:
- Cancer therapies significantly impact skin immunity.
- Understanding dermatotoxicity mechanisms enhances knowledge of skin biology.
- Various targeted agents and immunotherapies share common pathways affecting the skin.
Conclusions:
- Cancer therapy-induced dermatotoxicity provides valuable models for studying skin immunity.
- Further research is needed to elucidate remaining knowledge gaps.
- This understanding can lead to better management of side effects and improved cancer treatment strategies.
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