Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2003-5-28
pubmed:abstractText
Dietary omega-3 polyunsaturated fatty acids (omega-3 PUFAs) protect against photocarcinogenesis in animals, but prospective human studies are scarce. The mechanism(s) underlying the photoprotection are uncertain, although omega-3 PUFAs may influence oxidative stress. We examined the effect of supplementation on a range of indicators of ultraviolet radiation (UVR)-induced DNA damage in humans, and assessed effect on basal and post-UVR oxidative status. In a double-blind randomized study, 42 healthy subjects took 4 g daily of purified omega-3 PUFA, eicosapentaenoic acid (EPA), or monounsaturated, oleic acid (OA), for 3 months. EPA was bioavailable; the skin content at 3 months showing an 8-fold rise from baseline, P < 0.01. No consistent pattern of alteration in basal and UVR-exposed skin content of the antioxidants glutathione, vitamins E and C or lipid peroxidation, was seen on supplementation. Sunburn sensitivity was reduced on EPA, the UVR-induced erythemal threshold rising from a mean of 36 (SD 10) mJ/cm(2) at baseline to 49 (16) mJ/cm(2) after supplementation, P < 0.01. Moreover, UVR-induced skin p53 expression, assessed immunohistochemically at 24 h post-UVR exposure, fell from a mean of 16 (SD 5) positive cells/100 epidermal cells at baseline to 8 (4) after EPA supplementation, P < 0.01. Peripheral blood lymphocytes (PBL) sampled on 3 successive days both pre- and post-supplementation, showed no change with respect to basal DNA single-strand breaks or oxidative base modification (8-oxo-dG). However, when susceptibility of PBL to ex vivo UVR was examined using the comet assay, this revealed a reduction in tail moment from 84.4 (SD 3.4) at baseline to 69.4 (3.1) after EPA, P = 0.03. No significant changes were seen in any of the above parameters following OA supplementation. Reduction in this range of early markers, i.e. sunburn, UVR-induced p53 in skin and strand breaks in PBL, indicate protection by dietary EPA against acute UVR-induced genotoxicity; longer-term supplementation might reduce skin cancer in humans.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0143-3334
pubmed:author
pubmed:issnType
Print
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
919-25
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12771037-Adult, pubmed-meshheading:12771037-Aged, pubmed-meshheading:12771037-Ascorbic Acid, pubmed-meshheading:12771037-Biological Availability, pubmed-meshheading:12771037-DNA, pubmed-meshheading:12771037-DNA Damage, pubmed-meshheading:12771037-DNA Repair, pubmed-meshheading:12771037-Dietary Supplements, pubmed-meshheading:12771037-Double-Blind Method, pubmed-meshheading:12771037-Eicosapentaenoic Acid, pubmed-meshheading:12771037-Female, pubmed-meshheading:12771037-Genetic Markers, pubmed-meshheading:12771037-Glutathione, pubmed-meshheading:12771037-Humans, pubmed-meshheading:12771037-Lipid Peroxidation, pubmed-meshheading:12771037-Lymphocytes, pubmed-meshheading:12771037-Male, pubmed-meshheading:12771037-Middle Aged, pubmed-meshheading:12771037-Neoplasms, Radiation-Induced, pubmed-meshheading:12771037-Oleic Acid, pubmed-meshheading:12771037-Skin, pubmed-meshheading:12771037-Skin Neoplasms, pubmed-meshheading:12771037-Tumor Suppressor Protein p53, pubmed-meshheading:12771037-Ultraviolet Rays, pubmed-meshheading:12771037-Vitamin E
pubmed:year
2003
pubmed:articleTitle
Effect of eicosapentaenoic acid, an omega-3 polyunsaturated fatty acid, on UVR-related cancer risk in humans. An assessment of early genotoxic markers.
pubmed:affiliation
Photobiology Unit, Dermatology Centre, University of Manchester, UK. lesley.e.rhodes@man.ac.uk
pubmed:publicationType
Journal Article, Clinical Trial, Comparative Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't