Modulation of Skin Cancer by the Stimulator of Interferon Genes

Author:

Oscherwitz Max1,Jiminez Victoria1,Terhaar Hanna1,Yusuf Nabiha2ORCID

Affiliation:

1. Heersink School of Medicine, University of Alabama, Birmingham, AL 35294, USA

2. Department of Dermatology, University of Alabama, Birmingham, AL 35294, USA

Abstract

Morbidity and mortality from skin cancer continue to rise domestically and globally, and melanoma and non-melanoma skin cancers are a topic of interest in the dermatology and oncology communities. In this review, we summarize the stimulator of interferon genes (STING) pathway, its specific role in the pathogenesis of DNA damage and skin cancer, and STING-specific therapies that may fight both melanoma and non-melanoma skin (NMSC) cancers. Furthermore, we discuss specific portions of the STING pathway that may be used in addition to previously used therapies to provide a synergistic effect in future oncology treatments and discuss the limitations of current STING-based therapies.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference69 articles.

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3. Guy, G.P., Thomas, C.C., Thompson, T., Watson, M., Massetti, G.M., and Richardson, L.C. (2015). Melanoma Incidence and Mortality Trends and Projections—United States, 1982–2030, Ser. Vital Signs.

4. Prevalence and costs of skin cancer treatment in the U.S., 2002–2006 and 2007–2011;Guy;Am. J. Prev. Med.,2015

5. Identification of patients with nonmelanoma skin cancer using health maintenance organization claims data;Eide;Am. J. Epidemiol.,2010

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