Protection Against Pyrimidine Dimers, p53, and 8-hydroxy-2′-Deoxyguanosine Expression in Ultraviolet-Irradiated Human Skin by Sunscreens: Difference Between UVB + UVA and UVB Alone Sunscreens
As DNA damage induced by ultraviolet radiation plays an essential role in skin cancer induction, we pursued the measure of several DNA lesions induced by ultraviolet radiation in human skin for determining the efficacy of different topical photoprotectors. Non-exposed skin (buttocks from 20 individu...
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description | As DNA damage induced by ultraviolet radiation plays an essential role in skin cancer induction, we pursued the measure of several DNA lesions induced by ultraviolet radiation in human skin for determining the efficacy of different topical photoprotectors. Non-exposed skin (buttocks from 20 individuals) was exposed to 10 doses of ultraviolet, which corresponded to three to four minimal erythema doses of solar-simulating radiation, and biopsies were taken at 24 h within the half and one minimal erythema dose sites and a nonirradiated, adjacent control area. We report that even suberythemal doses of ultraviolet radiation are capable of inducing substantial DNA damage, namely pyrimidine dimers, p53 induction, and the DNA base-modified product generated by oxidative stress, 8-hydroxy-2′-deoxyguanosine. All three lesions are induced in a dose-dependent manner. An additional eight individuals were treated with either ultraviolet B or ultraviolet B + ultraviolet A sunblock (sun protection factor 15) and exposed to 7½ and 15 times the minimal erythema dose on each individual, with biopsies taken at 24 h post-ultraviolet. Pyrimidine dimer and p53 expression were rarely seen in nonirradiated skin but occasional staining was seen in all normal skin for 8-hydroxy-2′-deoxyguanosine. Applications of sunscreens to human skin before irradiation were shown to attenuate erythema but did not completely eliminate all three types of cellular damage when tested up to their sun protection factor 15. Furthermore, ultraviolet B + ultraviolet A sunscreens were less efficient than the ultraviolet B alone formulation for protection against all three lesions. These results suggest that DNA damage assessed in vivo by immunohistochemistry provides a very sensitive endpoint for determining the efficacy or photosensitivity of possible different protective measures in human skin. |
doi_str_mv | 10.1046/j.0022-202x.2001.01580.x |
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Non-exposed skin (buttocks from 20 individuals) was exposed to 10 doses of ultraviolet, which corresponded to three to four minimal erythema doses of solar-simulating radiation, and biopsies were taken at 24 h within the half and one minimal erythema dose sites and a nonirradiated, adjacent control area. We report that even suberythemal doses of ultraviolet radiation are capable of inducing substantial DNA damage, namely pyrimidine dimers, p53 induction, and the DNA base-modified product generated by oxidative stress, 8-hydroxy-2′-deoxyguanosine. All three lesions are induced in a dose-dependent manner. An additional eight individuals were treated with either ultraviolet B or ultraviolet B + ultraviolet A sunblock (sun protection factor 15) and exposed to 7½ and 15 times the minimal erythema dose on each individual, with biopsies taken at 24 h post-ultraviolet. Pyrimidine dimer and p53 expression were rarely seen in nonirradiated skin but occasional staining was seen in all normal skin for 8-hydroxy-2′-deoxyguanosine. Applications of sunscreens to human skin before irradiation were shown to attenuate erythema but did not completely eliminate all three types of cellular damage when tested up to their sun protection factor 15. Furthermore, ultraviolet B + ultraviolet A sunscreens were less efficient than the ultraviolet B alone formulation for protection against all three lesions. These results suggest that DNA damage assessed in vivo by immunohistochemistry provides a very sensitive endpoint for determining the efficacy or photosensitivity of possible different protective measures in human skin.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1046/j.0022-202x.2001.01580.x</identifier><identifier>PMID: 11886505</identifier><identifier>CODEN: JIDEAE</identifier><language>eng</language><publisher>Danvers, MA: Elsevier Inc</publisher><subject>8-OHdG ; Adult ; Biological and medical sciences ; Deoxyguanosine - analogs & derivatives ; Deoxyguanosine - analysis ; Deoxyguanosine - biosynthesis ; Diseases of the skin. Cosmetics ; DNA Damage ; erythema ; Erythema - pathology ; Erythema - prevention & control ; Humans ; Immunohistochemistry ; Medical sciences ; Middle Aged ; p53 ; pyrimidine dimers ; Pyrimidine Dimers - analysis ; Pyrimidine Dimers - metabolism ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Skin - chemistry ; Skin - metabolism ; Skin - radiation effects ; Sunscreening Agents - administration & dosage ; sunscreens ; Tumor Suppressor Protein p53 - analysis ; Tumor Suppressor Protein p53 - biosynthesis ; Ultraviolet Rays - adverse effects</subject><ispartof>Journal of investigative dermatology, 2001-12, Vol.117 (6), p.1437-1441</ispartof><rights>2001 The Society for Investigative Dermatology, Inc</rights><rights>2002 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Dec 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480x-f1d5cd8466212a1ef33b917a3d489c6b497a8a998d75650111416e0e4e2193b03</citedby><cites>FETCH-LOGICAL-c480x-f1d5cd8466212a1ef33b917a3d489c6b497a8a998d75650111416e0e4e2193b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/210370278?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,782,786,27931,27932,64392,64394,64396,72476</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13399734$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11886505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liardet, Stéphanie</creatorcontrib><creatorcontrib>Scaletta, Corinne</creatorcontrib><creatorcontrib>Panizzon, Renato</creatorcontrib><creatorcontrib>Hohlfeld, Patrick</creatorcontrib><creatorcontrib>Laurent-Applegate, Lee</creatorcontrib><title>Protection Against Pyrimidine Dimers, p53, and 8-hydroxy-2′-Deoxyguanosine Expression in Ultraviolet-Irradiated Human Skin by Sunscreens: Difference Between UVB + UVA and UVB Alone Sunscreens</title><title>Journal of investigative dermatology</title><addtitle>J Invest Dermatol</addtitle><description>As DNA damage induced by ultraviolet radiation plays an essential role in skin cancer induction, we pursued the measure of several DNA lesions induced by ultraviolet radiation in human skin for determining the efficacy of different topical photoprotectors. Non-exposed skin (buttocks from 20 individuals) was exposed to 10 doses of ultraviolet, which corresponded to three to four minimal erythema doses of solar-simulating radiation, and biopsies were taken at 24 h within the half and one minimal erythema dose sites and a nonirradiated, adjacent control area. We report that even suberythemal doses of ultraviolet radiation are capable of inducing substantial DNA damage, namely pyrimidine dimers, p53 induction, and the DNA base-modified product generated by oxidative stress, 8-hydroxy-2′-deoxyguanosine. All three lesions are induced in a dose-dependent manner. An additional eight individuals were treated with either ultraviolet B or ultraviolet B + ultraviolet A sunblock (sun protection factor 15) and exposed to 7½ and 15 times the minimal erythema dose on each individual, with biopsies taken at 24 h post-ultraviolet. Pyrimidine dimer and p53 expression were rarely seen in nonirradiated skin but occasional staining was seen in all normal skin for 8-hydroxy-2′-deoxyguanosine. Applications of sunscreens to human skin before irradiation were shown to attenuate erythema but did not completely eliminate all three types of cellular damage when tested up to their sun protection factor 15. Furthermore, ultraviolet B + ultraviolet A sunscreens were less efficient than the ultraviolet B alone formulation for protection against all three lesions. These results suggest that DNA damage assessed in vivo by immunohistochemistry provides a very sensitive endpoint for determining the efficacy or photosensitivity of possible different protective measures in human skin.</description><subject>8-OHdG</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Deoxyguanosine - analogs & derivatives</subject><subject>Deoxyguanosine - analysis</subject><subject>Deoxyguanosine - biosynthesis</subject><subject>Diseases of the skin. Cosmetics</subject><subject>DNA Damage</subject><subject>erythema</subject><subject>Erythema - pathology</subject><subject>Erythema - prevention & control</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>p53</subject><subject>pyrimidine dimers</subject><subject>Pyrimidine Dimers - analysis</subject><subject>Pyrimidine Dimers - metabolism</subject><subject>Radiotherapy. 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Cosmetics</topic><topic>DNA Damage</topic><topic>erythema</topic><topic>Erythema - pathology</topic><topic>Erythema - prevention & control</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>p53</topic><topic>pyrimidine dimers</topic><topic>Pyrimidine Dimers - analysis</topic><topic>Pyrimidine Dimers - metabolism</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Skin - chemistry</topic><topic>Skin - metabolism</topic><topic>Skin - radiation effects</topic><topic>Sunscreening Agents - administration & dosage</topic><topic>sunscreens</topic><topic>Tumor Suppressor Protein p53 - analysis</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><topic>Ultraviolet Rays - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liardet, Stéphanie</creatorcontrib><creatorcontrib>Scaletta, Corinne</creatorcontrib><creatorcontrib>Panizzon, Renato</creatorcontrib><creatorcontrib>Hohlfeld, Patrick</creatorcontrib><creatorcontrib>Laurent-Applegate, Lee</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of investigative dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liardet, Stéphanie</au><au>Scaletta, Corinne</au><au>Panizzon, Renato</au><au>Hohlfeld, Patrick</au><au>Laurent-Applegate, Lee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protection Against Pyrimidine Dimers, p53, and 8-hydroxy-2′-Deoxyguanosine Expression in Ultraviolet-Irradiated Human Skin by Sunscreens: Difference Between UVB + UVA and UVB Alone Sunscreens</atitle><jtitle>Journal of investigative dermatology</jtitle><addtitle>J Invest Dermatol</addtitle><date>2001-12</date><risdate>2001</risdate><volume>117</volume><issue>6</issue><spage>1437</spage><epage>1441</epage><pages>1437-1441</pages><issn>0022-202X</issn><eissn>1523-1747</eissn><coden>JIDEAE</coden><abstract>As DNA damage induced by ultraviolet radiation plays an essential role in skin cancer induction, we pursued the measure of several DNA lesions induced by ultraviolet radiation in human skin for determining the efficacy of different topical photoprotectors. Non-exposed skin (buttocks from 20 individuals) was exposed to 10 doses of ultraviolet, which corresponded to three to four minimal erythema doses of solar-simulating radiation, and biopsies were taken at 24 h within the half and one minimal erythema dose sites and a nonirradiated, adjacent control area. We report that even suberythemal doses of ultraviolet radiation are capable of inducing substantial DNA damage, namely pyrimidine dimers, p53 induction, and the DNA base-modified product generated by oxidative stress, 8-hydroxy-2′-deoxyguanosine. All three lesions are induced in a dose-dependent manner. An additional eight individuals were treated with either ultraviolet B or ultraviolet B + ultraviolet A sunblock (sun protection factor 15) and exposed to 7½ and 15 times the minimal erythema dose on each individual, with biopsies taken at 24 h post-ultraviolet. Pyrimidine dimer and p53 expression were rarely seen in nonirradiated skin but occasional staining was seen in all normal skin for 8-hydroxy-2′-deoxyguanosine. Applications of sunscreens to human skin before irradiation were shown to attenuate erythema but did not completely eliminate all three types of cellular damage when tested up to their sun protection factor 15. Furthermore, ultraviolet B + ultraviolet A sunscreens were less efficient than the ultraviolet B alone formulation for protection against all three lesions. These results suggest that DNA damage assessed in vivo by immunohistochemistry provides a very sensitive endpoint for determining the efficacy or photosensitivity of possible different protective measures in human skin.</abstract><cop>Danvers, MA</cop><pub>Elsevier Inc</pub><pmid>11886505</pmid><doi>10.1046/j.0022-202x.2001.01580.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 8-OHdG Adult Biological and medical sciences Deoxyguanosine - analogs & derivatives Deoxyguanosine - analysis Deoxyguanosine - biosynthesis Diseases of the skin. Cosmetics DNA Damage erythema Erythema - pathology Erythema - prevention & control Humans Immunohistochemistry Medical sciences Middle Aged p53 pyrimidine dimers Pyrimidine Dimers - analysis Pyrimidine Dimers - metabolism Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) Skin - chemistry Skin - metabolism Skin - radiation effects Sunscreening Agents - administration & dosage sunscreens Tumor Suppressor Protein p53 - analysis Tumor Suppressor Protein p53 - biosynthesis Ultraviolet Rays - adverse effects |
title | Protection Against Pyrimidine Dimers, p53, and 8-hydroxy-2′-Deoxyguanosine Expression in Ultraviolet-Irradiated Human Skin by Sunscreens: Difference Between UVB + UVA and UVB Alone Sunscreens |
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