The augmentation of melanocytic nevi in guinea pigs by solar-simulated light: An animal model for human melanocytic nevi

Cancer Research

Volumn 58, Issue 23, 1998, Pages 5361-5366

  Menzies, Scott ^a   Khalil, Mamdouh ^a   Crotty, Kerry ^b   Bonin, Antonio ^c  

^a ROYAL PRINCE ALFRED HOSPITAL   (Australia)

^b UNIVERSITY OF SYDNEY   (Australia)

^c National Institute of Occupational Health and Safety   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

7,12 DIMETHYLBENZ[A]ANTHRACENE; CARCINOGEN; DEOXYRIBODIPYRIMIDINE PHOTOLYASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; EXPERIMENTAL NEOPLASM; GUINEA PIG; HISTOPATHOLOGY; MELANOCYTIC NEVUS; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; SKIN CARCINOGENESIS; SKIN CELL; SOLAR RADIATION; SUN EXPOSURE; ULTRAVIOLET B RADIATION;

9,10-DIMETHYL-1,2-BENZANTHRACENE; ANIMALS; CARCINOGENS; CELL TRANSFORMATION, NEOPLASTIC; COCARCINOGENESIS; DEOXYRIBODIPYRIMIDINE PHOTO-LYASE; DISEASE MODELS, ANIMAL; DOSE-RESPONSE RELATIONSHIP, DRUG; GUINEA PIGS; HUMANS; MALE; NEVUS, PIGMENTED; SUNLIGHT;

EID: 0032403071     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (37)

1. Parkin, D., Muir, C., Whelan, S., Gao, Y., Ferlay, J., and Powell, J. (eds.). Cancer Incidence in Five Continents. IARC Scientific Publ. Lyon, France: IARC, 1992.
2. Elwood, J. M., and Koh, H. K. Etiology, epidemiology, risk factors, and public health issues of melanoma. Curr. Opin. Oncol., 6: 179-187, 1994.
3. Berwick, M., and Halpern, A. Melanoma epidemiology. Curr. Opin. Oncol., 9: 178-182, 1997.
4. Slade, J., Salopek, T., Marghoob, A., Kopf, A., and Rigel, D. Risk of developing cutaneous malignant melanoma in atypical-mole syndrome: New York University experience and literature review. In: C. Garbe, S. Schmitz, and C. Orfanos (eds.), Recent Results in Cancer Research 139 - Skin Cancer, pp. 87-104. Berlin: Springer-Verlag, 1995.
5. Luther, H., Altmeyer, P., Garbe, C., Ellwanger, U., Jahn, S., Hoffmann, K., and Segerling, M. Increase of melanocytic nevus counts in children during 5 years of follow-up and analysis of associated factors. Arch. Dermatol., 132: 1473-1478, 1996.
6. Dwyer, T., Blizzard, L., and Ashbolt, R. Sunburn associated with increased number of nevi in darker as well as lighter skinned adolescents of northern European descent. Cancer Epidemiol. Biomark. Prev., 4: 825-830, 1995.
7. Kelly, J., Rivers, J., MacLennan, R., Harrison, S., Lewis, A., and Tate, B. Sunlight: a major factor associated with the development of melanocytic nevi in Australian schoolchildren. J. Am. Acad. Dermatol., 30: 40-48, 1994.
8. Gallagher, R., McLean, D., Yang, C., Coldman, A., Silver, H., Spinelli, J., and Beagrie, M. Anatomic distribution of acquired melanocytic nevi in white children. A comparison with melanoma: the Vancouver mole study. Arch. Dermatol., 126: 466-471, 1990.
9. Friedman, R., Rigel, D., and Heilman, E. The relationship between melanocytic nevi and malignant melanoma. Dermatol. Clin. 6: 249-256, 1988.
10. Shapiro, R., Duquette, J., Roses, D., Nunes, I., Harris, M., Kamino, H., Wilson, E., and Rifkin, D. Induction of primary cutaneous melanocytic neoplasms in urokinase-type plasminogen activator (uPA)-deficient and wild-type mice: cellular blue nevi invade but do not progress to malignant melanoma in uPA-deficient animals. Cancer Res., 56: 3597-3604, 1996.
11. Chen, S., Zhu, H., Wetzel, W., and Philbert, M. Spontaneous melanocytosis in transgenic mice. J. Investig. Dermatol., 106: 1145-1151, 1996.
12. Millikan, L., Smith, L., and Ochsner, J. Animal models in melanoma. In: H. Maibach (ed.), Models in Dermatology, Vol. 1, pp. 22-33, Basel: Karger, 1985
13. Epstein, J. Experimental models for primary melanoma. Photodermatol. Photoimmunol. Photomed., 9: 91-98, 1992.
14. Ley, R., Applegate, L., Padilla, S., and Stuart, T. Ultraviolet radiation-induced malignant melanoma in Monodelphis domestica. Photochem. Photobiol., 50: 1-5, 1989.
15. Setlow, R., Woodhead, A., and Grist, E. Animal model for ultraviolet radiation-induced melanoma: platyfish-swordtail hybrid. Proc. Natl. Acad. Sci. USA, 86: 8922-8926, 1989.
16. Sancar, A. Structure and function of DNA photolyase. Biochemistry, 33: 2-9, 1994.
17. Kato, T., Todo, T., Ayaki, H., Ishizaki, K., Morita, T., Mitra, S., and Ikenaga, M. Cloning of a marsupial DNA photolyase gene and the lack of related nucleotide sequences in placental animals. Nucleic Acids Res. 22: 4119-4124, 1994.
18. Klein-Szanto, A., Silvers, W., and Mintz, B. Ultraviolet radiation-induced malignant skin melanoma in melanoma-susceptible transgenic mice. Cancer Res., 54: 4569-4572, 1994.
19. Takahashi, M., Iwamoto, T., and Nakashima, I. Proliferation and neoplastic transformation of pigment cells in metallothionein/ret transgenic mice. Pigm. Cell Res., 5: 344-347, 1992.
20. Husain, Z., Pathak, M., Flotte, T., and Wick, M. Role of ultraviolet radiation in the induction of melanocytic tumors in hairless mice following 7,12-dimethylbenz(a)anthracene application and ultraviolet radiation. Cancer Res., 51: 4964-4970, 1991.
21. Epstein, J., Epstein, W., and Nakai, T. Production of melanomas from DMBA-induced blue nevi in hairless mice with ultraviolet light. J. Natl. Cancer Inst., 38: 19-30, 1967.
22. Parrish, J. Responses of skin to visible and ultraviolet radiation. In: L. Goldsmith (ed.), Biochemistry and Physiology of the Skin, Vol. 2., pp. 713-733. New York: Oxford University Press, 1983.
23. Hook, R., Berkelhammer, J., and Oxenhandler, R. Sinclair swine melanoma. Am. J. Pathol., 108: 130-133, 1982.
24. Pawlowski, A., Haherman, H., and Menon, I. Skin melanoma induced by 7,12-dimethylbenzanthracene in albino guinea pigs and its similarities to skin melanoma of humans. Cancer Res., 40: 3652-3660, 1980.
25. Pawlowski, A., Haberman, H., and Menon, I. functional and compound pigmented nevi induced by 9,10-dimethyl-1,2-benzanthracene in skin of albino guinea pigs. Cancer Res., 36: 2813-2821, 1976.
26. Menzies, S. W., Greenoak, G. E., Reeve, V. E., and Gallagher, C. H. UV radiation-induced murine tumors produced in the absence of UV radiation-induced systemic tumor immunosuppression. Cancer Res., 51: 2773-2779, 1991.
27. Ley, R. Photoreactivation of UV-induced pyrimidine dimers and erythema in the marsupial Monodelphis domestica. Proc. Natl. Acad. Sci. USA, 82: 2409-2411, 1985.
28. Ruiter, D., and Brocker, E. Immunohistochemistry in the evaluation of melanocytic tumours. Semin. Diagn. Pathol., 10: 76-91, 1993.
29. Bacchi, C. E., Bonetti, F., Pea, M., Martignoni, G., and Gown, A. HMB-45. A review. Appl. Immunohistochem., 4: 73-85, 1996.
30. Bolognia, J., Murray, M., and Pawelek, J. Hairless pigmented guinea pigs: a new model for the study of mammalian pigmentation. Pigm. Cell Res., 3: 150-156, 1990.
31. Barnhill, R., and Mihm, M. The histopathology of cutaneous malignant melanoma. Semin. Diagn. Pathol., 10: 47-75, 1993.
32. Sutherland, B., and Bennett, P. Human white blood cells contain cyclobutyl pyrimidine dimer photolyase. Proc. Natl. Acad. Sci. USA, 92: 9732-9736, 1995.
33. Kusewitt, D., Applegate, L., and Ley, R. Ultraviolet radiation-induced skin tumors in a South American opossum (Monodelphis domestica). Vet. Pathol., 28: 55-65, 1991.
34. Voulot, C., and Laviolette, P. Les tyrosinases des parties pigmentees de l'oeil chez quatre ezpeces de Rongeurs. C. R. Acad. Sci. Hebd. Seances. Acad. Sci. D., 283: 79-81, 1976.
35. Poland, A., Palen, D., and Glover, E. Tumour promotion by TCDD in skin of HRS/J hairless mice. Nature (Lond.), 300: 271-273, 1982.
36. Hisoire, G., and Bucks, D. An unexpected finding in percutaneous absorption observed between haired and hairless guinea pig skin. J. Pharm. Sci., 86: 398-400, 1997.
37. Horio, T., Miyauchi, H., and Asada, Y. The hairless guinea pig as an experimental animal for photodermatology. Photodermatol. Photoimmunol. Photomed., 8: 69-72, 1991.