References
Albino, A. P.; Le Strange, R.; Oliff, A. I., et al. Transforming ras genes from human melanoma: a manifestation of tumor heterogeneity? Nature 308:69–71; 1984.
Albino, A. P.; Nanus, D. M.; Mentle, I. R., et al. Analysis of ras oncogenes in malignant melanoma and precursor lesions: correlation of point mutations with differentiation phenotype. Oncogene 4:1363–1374; 1989.
Atkin, N. B.; Baker, M. C. Abnormal chromosomes including small metacentrics in 14 ovarian cancers. Cancer Genet. Cytogenet. 26:355–361; 1987.
Akslen, L. A.; Morkve, O. Expression of p53 protein in cutaneous melanoma. Intl. J. Cancer 52:13–16; 1992.
Balaban, G.; Herlyn, M.; DuPont, G. N., et al. Cytogenetics of human malignant melanoma and premalignant lesions. Cancer Genet. Cytogenet. 11:429–439; 1984.
Balaban, G. B.; Herlyn, M.; Clark, W. H., et al. Karyotypic evolution in human malignant melanoma. Cancer Genet. Cytogenet. 19:113–122; 1986.
Becher, R.; Gibas, Z.; Karakousis, C., et al. Nonrandom chromosome changes in malignant melanoma. Cancer Res. 43:5010–5016; 1983.
Cowan, J. M.; Francke, U. Cytogenetic analysis in melanoma and nevi. In: Nathanson, L., ed. Melanoma research: genetics, growth factors, metastasis and antigens. New York: Kluwer Academic Publishers; 1991:3–16.
Cowan, J. M.; Halaban, R.; Francke, U. Cytogenetic analysis of melanocytes from premalignant nevi and melanomas. JNCI 80:1159–1164; 1988.
Fountain, J. W.; Bale, S. J.; Housman, D. E., et al. Genetics of melanoma. Cancer Surv. 9:646–665; 1990.
Fountain, J. W.; Karayiorgou, M.; Ernstoff, M. S., et al. Homozygous deletions within human chromosome band 9p21 in melanoma. Proc. Natl. Acad. Sci. USA 89:10557–10561; 1992.
Francke, U.; De Martinville, B.; Coussens, L., et al. The human gene for the p-subunit of nerve growth factor is located on the proximal short arm of chromosome 1. Science 222:1248–1251; 1983.
Harper, M. E.; Franchini, C.; Love, J., et al. Chromosomal sublocalization of human c-myb and c-fis cellular oncogenes. Nature 304:169–171; 1983.
Horsthemke, B.; Prescher, G.; Bornfeld, N., et al. Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanoma. Genes Chromosomes Cancer 4:217–221; 1992.
Harnden, D. G.; Klinger, H. P., editors. ISCN. An international system for human cytogenetic nomenclature. Basel: Karger; 1991. (Published in collaboration with Cytogenet Cell Genet. Also in Birth Defects: Original Article Series, 21: 1985).
Isobe, M.; Emanuel, B. S.; Givol, D., et al. Localization of gene for human p53 tumor antigen to band 17p13. Nature 320:84–85; 1986.
Knowles, B. B.; Stolter, D.; Trimcheri, G., et al. Complement-mediated antiserum cytotoxic reactions to human chromosome coded antigen(s): immunoselection of rearranged human chromosome 7 in human-mouse somatic cell hybrids. J. Exp. Med. 145:314–326; 1977.
Kondo, I.; Shimizu, N. Mapping of the gene for epidermal growth factor receptor (EGFR) on the p13–q22 region of chromosome 7. Cytogenet. Cell Genet. 35:9–14; 1983.
Koprowski, H.; Herlyn, M.; Balaban, G., et al. Expression of the receptor for epidermal growth factor correlates with increased dosage of chromosome 7 in malignant melanoma. Somatic Cell Mol. Genet. 11:297–302; 1985.
Limon, J.; Cir Dal, P.; Sait, S. N. J., et al. Chromosome changes in metastatic human melanoma. Cancer Genet. Cytogenet. 30:201–211; 1988.
Levine, A. J.; Momand, J.; Finlay, C. A. The p53 tumor suppressor gene. Nature 351:453–456; 1991.
McBride, O. W.; Merry, D.; Gival, D. The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm. Proc. Natl. Acad. Sci. USA 83:130–134; 1986.
Mitelman, F.; Heim, S. Consistent involvement of only 71 of the 329 chromosomal bands of the human genome in primary neoplasia-associated rearrangements. Cancer Res. 45:7115–7119; 1988.
Pathak, S.; Drwinga, H. L.; Hsu, T. C. Involvement of chromosome 6 in rearrangements in human malignant melanoma cell lines. Cytogenet. Cell Genet. 36:573–579; 1983.
Pearson, M.; Rowly, J. D. The relation of oncogenesis and cytogenetics in leukemia and lymphoma. Annu. Rev. Med. 36:471–482; 1985.
Pedersen, M. I.; Bennet, J. W.; Wang, N. Nonrandom chromosome structural aberrations and oncogene loci in human malignant melanoma. Cancer Genet. Cytogenet. 20:11–27; 1986.
Rooney, D. E.; Czepulkowski, B. H. Human cytogenetics: a practical approach, Washington DC: IRL Press; 1986:61–65.
Sandberg, A. A. The chromosomes in human cancer and leukemia. New York: Elsevier North Holland; 1980:776.
Sisley, K.; Cottam, D. W.; Rennie, I. G., et al. Non-random abnormalities of chromosomes 3, 6, and 8 associated with posterior uveal melanoma. Genes Chromosomes Cancer 5:197–200; 1992.
Squire, J.; Phillips, R. A.; Boyce, S., et al. Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: verification by standard standing techniques, new densitometers methods, and somatic cell hybridization. Hum. Genet. 66:46–53; 1984.
Stretch, J. R.; Gatter, K. C.; Raljkiar, E., et al. Expression of mutant p53 in melanoma. Cancer Res. 51:5976–5979; 1991.
Trent, J. M.; Leung, S. P. L.; Meyskens, F. L. Chromosome alterations in human malignant melanoma. In: Conti, C. J., ed. Skin tumors: experimental and clinical aspects. New York: Raven Press; 1989:165–186.
Trent, J. M.; Stanbridge, E. J.; McBride, H. L., et al. Tumorigenicity in human melanoma cell lines controlled by introduction of human chromosome 6. Science 247:568–571; 1990.
Veer, L. J.; Burgering, M. T.; Versteeg, R., et al. N-ras mutations in human cutaneous melanoma from sun-exposed body sites. Mol. Cell Biol. 9:3114–3116; 1989.
Verma, R. S.; Babu, A. Human chromosomes: manual of basic techniques. New York: Pergamon Press; 1980:47–48.
Yunis, J. J. The chromosomal basis of human neoplasia. Science 221:227–236; 1983.
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Rauth, S., Green, A., Bratescu, L. et al. Chromosome abnormalities in metastatic melanoma. In Vitro Cell Dev Biol - Animal 30, 79–84 (1994). https://doi.org/10.1007/BF02631396
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DOI: https://doi.org/10.1007/BF02631396