Broad-spectrum moisturizer effectively prevents molecular reactions to UVA radiation.

The damaging effects of UVA radiation have been well-documented. UVA radiation is known to induce molecular, cellular, and clinical damage. Such harm may lead to photoaging, immune system depression, altered gene expression, or oncogene and tumor suppressor gene modulation, all of which are partly responsible for the development of skin cancer. In parallel to an increased understanding of the added damage caused by UVA radiation, progress has been made in sunscreen formulation. A variety of UVA filters are now available for formulators to combine with UVB filters to reach high-level photostable protection using a minimum concentration of active ingredients. The efficacy of products that contain these UV filter combinations usually is determined by noninvasive assessments, which cause either UVA-induced erythema or skin pigmentation. However, the biologic relevance of these end points for UVA radiation-induced skin damage is unknown. In our study, we confirm that the assessment of UVA radiation-induced gene expression in skin specimens obtained from UVA-irradiated human skin by quantitative real-time polymerase chain reaction is a sensitive, reliable, and robust method to prove the efficacy of 2 daily moisturizers containing broad-spectrum sunscreen. Specifically, we demonstrate in vivo that topical application of a daily moisturizer with broad-spectrum sunscreen prevents UVA radiation-induced transcriptional expression of genes that are directly linked to skin aging (ie, matrix metalloproteinase 1 [MMP-1]) and also reflect the skin's antioxidative stress defense response (ie, catalase [CAT], superoxide dismutase [SOD], glutathione peroxidase [GPx]). Furthermore, we demonstrate that the protection against UV-induced skin damage provided by products with different sun protection factor (SPF) but the same UVA protection factor (UVA-PF) is similar, which emphasizes the importance of high UVA protection to maintain unaltered essential biologic functions. These data indicate that the use of a daily moisturizer containing broad-spectrum sunscreen with a well-balanced SPF/UVA-PF ratio on a regular basis is beneficial for human skin.

[1]  S. Seité,et al.  UVA filters in sun-protection products: regulatory and biological aspects , 2012, Photochemical & Photobiological Sciences.

[2]  D. Moyal The development of efficient sunscreens. , 2012, Indian journal of dermatology, venereology and leprology.

[3]  S. Seité,et al.  A broad‐spectrum sunscreen prevents UVA radiation‐induced gene expression in reconstructed skin in vitro and in human skin in vivo , 2011, Experimental dermatology.

[4]  S. Seité,et al.  Photodamage to human skin by suberythemal exposure to solar ultraviolet radiation can be attenuated by sunscreens: a review , 2010, The British journal of dermatology.

[5]  M. Weinstock,et al.  Indoor Tanning and Risk of Melanoma: A Case-Control Study in a Highly Exposed Population , 2010, Cancer Epidemiology, Biomarkers & Prevention.

[6]  B. Diffey Sunscreens: expectation and realization , 2009, Photodermatology, photoimmunology & photomedicine.

[7]  S. Seité,et al.  Novel Developments in Photoprotection: Part II , 2007 .

[8]  F. Bernerd,et al.  Matrix Metalloproteinase‐1 Production Observed After Solar‐Simulated Radiation Exposure is Assumed by Dermal Fibroblasts but Involves a Paracrine Activation Through Epidermal Keratinocytes ¶ , 2004, Photochemistry and photobiology.

[9]  C. Garland,et al.  Epidemiologic evidence for different roles of ultraviolet A and B radiation in melanoma mortality rates. , 2003, Annals of epidemiology.

[10]  F. Bernerd,et al.  The sun protection factor (SPF) inadequately defines broad spectrum photoprotection: demonstration using skin reconstructed in vitro exposed to UVA, UVBor UV-solar simulated radiation. , 2003, European journal of dermatology : EJD.

[11]  B. Diffey,et al.  Sources and measurement of ultraviolet radiation. , 2002, Methods.

[12]  G. Halliday,et al.  Ultraviolet a augments solar-simulated ultraviolet radiation-induced local suppression of recall responses in humans. , 2002, The Journal of investigative dermatology.

[13]  A. Chardon,et al.  In vivo measurement of the photostability of sunscreen products using diffuse reflectance spectroscopy , 2002, Photodermatology, photoimmunology & photomedicine.

[14]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[15]  D H Sliney,et al.  UV Doses of Americans¶ , 2001, Photochemistry and photobiology.

[16]  N. Kollias,et al.  UVA protection efficacy of sunscreens can be determined by thepersistent pigment darkening (PPD) method , 2000, Photodermatology, photoimmunology & photomedicine.

[17]  N. Kollias,et al.  Determination of UVA protection factors using the persistent pigment darkening (PPD) as the end point , 2000, Photodermatology, photoimmunology & photomedicine.

[18]  F. Bernerd,et al.  Evaluation of the Protective Effect of Sunscreens on In Vitro Reconstructed Human Skin Exposed to UVB or UVA Irradiation , 2000, Photochemistry and photobiology.

[19]  F. Bernerd,et al.  UVA exposure of human skin reconstructed in vitro induces apoptosis of dermal fibroblasts: subsequent connective tissue repair and implications in photoaging , 1998, Cell Death and Differentiation.

[20]  R. Lavker,et al.  The spectral dependence for UVA-induced cumulative damage in human skin. , 1997, The Journal of investigative dermatology.

[21]  S. González,et al.  Drug photosensitivity, idiopathic photodermatoses, and sunscreens. , 1996, Journal of the American Academy of Dermatology.

[22]  George I. Bell,et al.  Sequence of a cDNA coding for human glutathione peroxidase confirms TGA encodes active site selenocysteine , 1987, Nucleic Acids Res..

[23]  A D Pearse,et al.  Epidermal changes in human skin following irradiation with either UVB or UVA. , 1987, The Journal of investigative dermatology.

[24]  F. Quan,et al.  Isolation and characterization of the human catalase gene , 1986, Nucleic Acids Res..

[25]  A. Eisen,et al.  Human fibroblast collagenase. Complete primary structure and homology to an oncogene transformation-induced rat protein. , 1986, The Journal of biological chemistry.

[26]  H. Hönigsmann,et al.  Polymorphous light eruption: action spectrum and photoprotection. , 1986, Journal of the American Academy of Dermatology.

[27]  B. Maden,et al.  Human 18 S ribosomal RNA sequence inferred from DNA sequence. Variations in 18 S sequences and secondary modification patterns between vertebrates. , 1985, The Biochemical journal.

[28]  H Slaper,et al.  TRANSMISSION OF HUMAN EPIDERMIS AND STRATUM CORNEUM AS A FUNCTION OF THICKNESS IN THE ULTRAVIOLET AND VISIBLE WAVELENGTHS , 1984, Photochemistry and photobiology.

[29]  Y. Groner,et al.  Nucleotide sequence and expression of human chromosome 21-encoded superoxide dismutase mRNA. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[30]  M. Ichihashi,et al.  Solar urticaria. Determinations of action and inhibition spectra. , 1982, Archives of dermatology.

[31]  A. Kligman,et al.  The acute effects of long-wave ultraviolet radiation on human skin. , 1979, The Journal of investigative dermatology.