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Ronald D Ley

Publications and source records attributed to Ronald D Ley.

4 recordsLinked to original sources

UV causation of melanoma in Xiphophorus is dominated by melanin photosensitized oxidant production.

Controversy continues both as to which wavelengths of sunlight cause melanoma and the mechanisms by which these different wavelengths act. Direct absorption of UVB by DNA is central in albino animal models, but melanin-pigmented models have shown major contributions by wavelengths longer than UVB that are thought to be mediated by photosensitized oxidant production. The only model for which the action spectrum of melanoma causation is known is a genetically melanoma-susceptible specific cross of Xiphophorus fish. We used electron paramagnetic resonance to quantitatively detect the UV induction of reactive melanin radicals in situ in the melanin-containing cells in the skin of this model and derived the action spectrum for melanin-photosensitized oxidant production (Phi(ox)). This action spectrum was identical to that for melanoma induction (Phi(mel)). These results confirm the hypothesis that melanin-photosensitized radical production is the major causative step of melanoma in this model and demonstrate that the wavelengths and mechanisms of melanoma causation in different models are dependent on the presence of melanin. This approach should be applicable to humans, thus providing an accurate surrogate for Phi(mel) for prevention studies.

Animals↗

Standardized protocols for photocarcinogenesis safety testing.

Solar ultraviolet radiation (UVR) is recognized as a major cause of non-melanoma skin cancer in man. Skin cancer occurs most frequently in the most heavily exposed areas and correlates with degree of outdoor exposure. The incidence of skin cancer is also increased by contact with photosensitizing drugs and chemicals such as psoralens, coal tars and petroleum stocks. Other substances which do not act as photosensitizers, such as immunosuppressants taken by organ transplant recipients, also increase the risk of skin cancer. The U.S. Food and Drug Administration requests, on a case-by-case basis, that risk of enhanced photocarcinogenesis is assessed for many classes of drugs. Health Canada's Therapeutic Products Programme has issued a Notice of Intent to regulate pharmaceutical products which may enhance carcinogenicity of the skin induced by ultraviolet radiation. Other national regulatory agencies review such data when they exist, but their own requirements emphasize batteries of short-term in vitro and in vivo tests. While they may support drug development strategies, short-term tests have yet to be validated as predictors of the ability of drugs or chemicals to enhance photocarcinogenesis. Published protocols now describe study designs and procedures capable of determining whether test agents enhance the rate of formation of UVR-induced skin tumors.

Animals↗

Animal models of ultraviolet radiation (UVR)-induced cutaneous melanoma.

The incidence of cutaneous melanoma continues to increase in many parts of the world including the United States. The American Cancer Society predicts that there will be approximately 53,600 new cases of melanoma in the United States during 2002 and that there will be 7,400 deaths from melanoma during the same time period. Increased understanding of the underlying mechanisms and risk factors involved in the induction of this deadly disease will require the use of suitable animal models of melanoma. To date, the induction of cutaneous melanoma with ultraviolet radiation (UVR) alone has been observed only in a few diverse animal models: a South American opossum, Monodelphis domestica; a hybrid fish, Xiphophorus; several stocks of transgenic mice; and in Angora goats. Most of these models are not completely suitable due to: 1) the target cell for melanoma formation; 2) the location of the melanocytes in the skin (i.e.- dermal as opposed to epidermal in humans); or 3) problems associated with husbandry and experimental manipulation. Recent studies have identified a mouse, the hepatocyte growth factor/scatter factor (HGF/SF) transgenic mouse, as an attractive model with which to study the induction of melanoma following a single, neonatal exposure to a moderate dose of UVR.

Animals↗

Comparison between ultraviolet-visible and near-infrared elastic scattering spectroscopy of chemically induced melanomas in an animal model.

The work reported compares elastic scattering spectroscopy (ESS) for diagnosis of pigmented skin lesions in two spectral regions: UV-visible and near infrared (NIR). Given the known strong absorption by melanin in the near-UV to mid-visible range of the spectrum, such a comparison can help determine the optimum wavelength range of ESS for diagnosis of pigmented skin lesions. For this purpose, four South American opossums are treated with dimethylbenz(a)anthracene on multiple dorsal sites to induce both malignant melanomas and benign pigmented lesions. Skin lesions are examined in vivo with ESS using both UV-visible and NIR, with wavelength ranges of 330 to 900 nm and 900 to 1700 nm, respectively. Both portable systems use the same fiber optic probe geometry. ESS measurements are made on the lesions, and spectral differences are grouped by diagnosis from standard histopathological procedure. Both ESS datasets show strong spectral trends with the histopathological assignments, and the data suggest a model for the underlying basis of the spectral distinction between benign and malignant pigmented nevi.

9,10-Dimethyl-1,2-benzanthracene↗