Literature DB >> 26355618

Comparative Effects of Sunscreens Alone vs Sunscreens Plus DNA Repair Enzymes in Patients With Actinic Keratosis: Clinical and Molecular Findings from a 6-Month, Randomized, Clinical Study.

Mauro Carducci, Paolo Sergio Pavone, Giuseppe De Marco, Silvia Lovati, Velimir Altabas, Karmela Altabas, Enzo Emanuele.   

Abstract

Recent experimental irradiation studies have shown that the addition of DNA repair enzymes (photolyase and endonuclease) to traditional sunscreens may reduce ultraviolet radiation (UVR)-induced molecular damage to the skin to a greater extent than sunscreens alone. In this 6-month, randomized, clinical study, we sought to compare the clinical and molecular effects of sunscreens plus DNA repair enzymes vs. those of traditional sunscreens alone in patients with actinic keratosis (AK). A total of 28 AK patients were randomized to topically apply sunscreens plus DNA repair enzymes (enzyme group; n = 14) or sunscreens alone (sunscreen group; n = 14) for 6 months. The main outcome measures included 1) hyperkeratosis, 2) field cancerization (as measured by fluorescence diagnostics using methylaminolaevulinate), and 3) levels of cyclobutane pyrimidine dimers (CPDs) in skin biopsies. Both regimens produced a significant reduction of hyperkeratosis at 6 months, with no difference between the two groups. Field cancerization was significantly reduced by both regimens, but the decrease observed in the enzyme group was significantly more pronounced than in the sunscreen group (P < 0.001). At 6 months, CPDs decreased by 61% in the enzyme group and by 35% in the sunscreen group compared with baseline values (P < 0.001). These findings indicate that, despite a similar effect on hyperkeratosis, the addition of DNA repair enzymes to sunscreens was more effective in reducing field cancerization and CPDs than sunscreens alone. Taken together, our findings indicate that sunscreens plus DNA repair enzymes may be superior to traditional sunscreens alone in reducing field cancerization and UVR-associated molecular signatures (CPDs) in AK patients, potentially preventing malignant transformation into invasive squamous cell carcinoma in a more efficient manner.

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Year:  2015        PMID: 26355618

Source DB:  PubMed          Journal:  J Drugs Dermatol        ISSN: 1545-9616            Impact factor:   2.114


  5 in total

Review 1.  [Sunscreens of the future: challenges and opportunities].

Authors:  Peter Wolf; Jean Krutmann
Journal:  Hautarzt       Date:  2022-03-08       Impact factor: 0.751

2.  DNA photolyase from Antarctic marine bacterium Rhodococcus sp. NJ-530 can repair DNA damage caused by ultraviolet.

Authors:  Yingying He; Changfeng Qu; Liping Zhang; Jinlai Miao
Journal:  3 Biotech       Date:  2021-01-29       Impact factor: 2.406

Review 3.  Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage.

Authors:  Rhonda M Brand; Peter Wipf; Austin Durham; Michael W Epperly; Joel S Greenberger; Louis D Falo
Journal:  Front Pharmacol       Date:  2018-08-20       Impact factor: 5.810

4.  Six critical questions for DNA repair enzymes in skincare products: a review in dialog.

Authors:  Daniel B Yarosh; Amanda Rosenthal; Ronald Moy
Journal:  Clin Cosmet Investig Dermatol       Date:  2019-08-29

5.  AKASI and Near-Infrared Spectroscopy in the combined effectiveness evaluation of an actinic keratoses preventive product in immunocompetent and immunocompromised patients.

Authors:  Federica Veronese; Silvia Seoni; Vanessa Tarantino; Matteo Buttafava; Chiara Airoldi; Kristen M Meiburger; Elisa Zavattaro; Paola Savoia
Journal:  Front Med (Lausanne)       Date:  2022-09-07
  5 in total

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