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Review
. 2022 Feb;12(2):361-380.
doi: 10.1007/s13555-021-00644-3. Epub 2022 Feb 3.

Exposome and Skin. Part 2. The Influential Role of the Exposome, Beyond UVR, in Actinic Keratosis, Bowen's Disease and Squamous Cell Carcinoma: A Proposal

Affiliations
Review

Exposome and Skin. Part 2. The Influential Role of the Exposome, Beyond UVR, in Actinic Keratosis, Bowen's Disease and Squamous Cell Carcinoma: A Proposal

Manuel Molina-García et al. Dermatol Ther (Heidelb). 2022 Feb.

Abstract

Actinic keratosis (AK) is the main risk factor for the development of cutaneous invasive squamous cell carcinoma (SCC). It represents the first sign of severe chronic ultraviolet radiation exposure, which has a clear significant effect. Nevertheless, the skin is exposed to many other exposome factors which should be thoroughly considered. Our aim was to assess the impact of exposome factors other than ultraviolet radiation (UVR) on the etiopathology of AK and Bowen's disease (BD) and progression of AK to SCC and to design tailored prevention strategies. We performed an exhaustive literature search in September 2021 through PubMed on the impact of exposome factors other than UVR on AK, BD and SCC. We conducted several parallel searches combining terms of the following topics: AK, BD, SCC and microbiome, hormones, nutrition, alcohol, tobacco, viral infections, chemical contaminants and air pollution. Notably, skin microbiome studies have shown how Staphylococcus aureus infections are associated with AK and AK-to-SCC progression by the production of chronic inflammation. Nutritional studies have demonstrated how a caloric restriction in fat intake, oral nicotinamide and moderate consumption of wine significantly reduce the number of premalignant keratoses and SCC. Regarding lifestyle factors, both alcohol and smoking are associated with the development of SCC in a dose-dependent manner. Relevant environmental factors are viral infections and chemical contaminants. Human papillomavirus infections induce deregulation of cellular proliferation and are associated with AK, BD and SCC. In addition to outdoor jobs, occupations such as industrial processing and farming also increase the risk of developing keratoses and SCC. The exposome of AK will undoubtedly help the understanding of its etiopathology and possible progression to SCC and will serve as a basis to design tailored prevention strategies.

Keywords: Actinic keratosis; Dermatology; Environmental factors; Exposome; Hormones; Microbiome; Nutrition; Pollution; Prevention strategies; Squamous cell carcinoma.

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Figures

Fig. 1
Fig. 1
Schematic map of the host, nutritional, lifestyle and environmental factors influencing AK, BD and SCC

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References

    1. Marks R, Rennie G, Selwood TS. Malignant transformation of solar keratoses to squamous cell carcinoma. Lancet. 1988;1(8589):795–797. - PubMed
    1. Berker D, McGregor JM, Hughes BR, British Association of Dermatologists Therapy Guidelines and Audit Subcommittee Guidelines for the management of actinic keratoses. Br J Dermatol. 2007;156:222–230. - PubMed
    1. Stockfleth E, Kerl H, Guideline Subcommittee of the European Dermatology Forum Guidelines for the management of actinic keratoses. Eur J Dermatol. 2006;16:599–606. - PubMed
    1. Heaphy MR, Jr, Ackerman AB. The nature of solar keratosis: a critical review in historical perspective. J Am Acad Dermatol. 2000;43(1 Pt 1):138–150. - PubMed
    1. De Oliveira ECV, da Motta VRV, Pantoja PC, et al. Actinic keratosis—review for clinical practice. Int J Dermatol. 2019;58(4):400–407. - PubMed