Involvement of chromosome 6 in rearrangements in human malignant melanoma cell lines

Cytogenetics and Cell Genetics

Volumn 36, Issue 3, 1983, Pages 573-579

  Pathak, S ^a,b   Drwinga, H L ^c   Hsu, T C ^a,b  

^a UNIVERSITY OF TEXAS   (United States)

^b UNIVERSITY OF TEXAS   (United States)

^c Vermont Studies Group   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL LINE; CHROMOSOME 6 ABERRATION; CHROMOSOME TRANSLOCATION 6; ETIOLOGY; HEREDITY; HISTOLOGY; HUMAN; IN VITRO STUDY; MAJOR CLINICAL STUDY; MELANOMA;

CELL LINE; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, 6-12 AND X; FEMALE; HUMAN; KARYOTYPING; MALE; MELANOMA; SUPPORT, NON-U.S. GOV'T; TRANSLOCATION (GENETICS);

EID: 0021076337     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000131975     Document Type: Article

References (37)

1. Anderson, D.E.; Smith. J.L., and McBride. C.M.: Hereditary aspects of malignant melanoma. J. Am. med. Ass. 200: 741-746 (1967).
2. Atkin, N.B. and Baker. M.C: A metastatic malignant melanoma with 24 chromosomes. Hum. Genet. 58: 217-219 (1981).
3. Balaban, G: Gilbert. F.; Nichols. W.; Meadows, A.T. and Shields. J.: Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes. Cancer Genet. Cytogenet. 6: 213-221 (1982).
4. Berger, R.; Bernheim. A.; Weh, N.J.; Flandrin. G.; Daniel. M.T.; Brouet. J.C. and Colbert. N.: A new translocation in Burkitt's tumor cells. Hum. Genet. 53: 111-112 (1979).
5. Chen, T.R. and Shaw, M.W.: Stable chromosome changes in a human malignant melanoma. Cancer Res. 33: 2042-2047 (1973).
6. Chen, T.R. and Shaw. M.W.: Sludies of a cell line derived from a human malignanl melanoma. in Vitro 10: 216-224 (1974).
7. Crucigcr, Q.V.J.; Pathak. S., and Cailleau. R.: Human breast carcinomas: Marker chromosomes involving lq in seven cases. Cytogenet. Cell Genet 17: 231-235 (1976).
8. Dalla-Favcra. R.; Franchini, G.; Martinoiti. S.; Wong-Staal. F.; Gallo. R.C, and Croce, C.M.: Chromosomal assignment of the human homologues of feline sarcoma virus and iivian myeloblastosis virus One genes. Proe. natn. Acad. Sci. USA 79: 4714-4717 (1982).
9. Fraccaro, M.; Locurto. F. and Scappaticci. S.: Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41). Chromosomes Today 5: 265-280 (1976).
10. Gilbert, F.; Balaban. G.; Moorhcad. P.; Bianchi. D., and Schlesinger, H.: Abnormalities of chromosome lp in human neuroblastoma tumors and cell lines. Cancer Genet. Cytogenet. 7: 33-42 (1982).
11. Gleicher, N.; Cohen, C.J.; Deppe. G, and Ciusberg. S. B.: Familial malignanl melanoma of the female genitalia: a case repon and review. Obstet. Gyn. Surv. 84: 1-15 (1979).
12. Hawkins, B.R.; Dawkins. R.L.; Hockey. A.; Houlision. J. B. and Kirk. R.L.: Evidence for linkage between HLA and malignanl melanoma. Tissue Antigens 17: 540-541 (1981).
13. Kakati, S.; Oshimura. M. and Sandberg, A.A.: The chromosomes and causation of human cancer and leukemia. XIX. Commini markers in various tumors. Cancer 38: 770-777 (1976).
14. Kakati, S.; Song. S.Y., and Sandberg. A.A.: Chromosomes and causation of human cancer and leukemia. XXII. Karyotypic changes in malignanl melanoma. Cancer 40: 1173-1181 (1977).
15. Kaneko, Y.; Egucs. M.C. and Rowley. J.D.: Interstitial deletion of short arm of chromosome 11 limited 10 Wilms' tumor cells in a patient without aniridia. Cancer Res. 41: 4577-4578 (1981).
16. Kovacs, G.: Abnormalities of chromosome no. I in human solid malignant tumors. Int. J. Cancer 21: 688-694 (1978).
17. Kusnctsova, L.E.; Prigogina. E.L.; Pogosianz. H.E. and Belkina, B. M.: Similar chromosomal abnormalities in several retino-blastomas. Hum. Genet. 61: 201-204 (1982).
18. Lamm, L. U.; Kissmeyer-Nielsen. F.; Kjerbyc. K.E.; Mogensen, B., and Petersen. N.C: HL-A and ABO antigens and malignanl melanoma: a study of 212 eases. Cancer 33: 1458-1461 (1974).
19. Mark, J.; Levan. G., and Milelman. F.: Identification by fluorescence of the G chromosome lost in human meningiomas. Hereditas 71: 163-168 (1972).
20. McCulloch. P. B.; Dent. P. B.; Hayes, P.R. and Liao. S. K.: Common and individually specific chromosomal characteristics of culiured human melanoma. Cancer Res. 36: 398-404 (1976).
21. Milelman, F. and Levan. G.: Clustering of aberrations lo specific chromosomes in human neoplasms. IV. A survey of 1,871 cases. Hereditas 95: 79-139 (1981).
22. Miyoshi, S.; Hiraki. S.; Kimura. K.; Miyamoto, K., and Sato. J.: 2/8 Translocation in a Japanese Burkiu's lymphoma. Experientia 35: 742-743 (1979).
23. Muir, P.D. and Gunz. F.W.: A cytogenetic study of eight human melanoma cell lines. Pathology 11: 597-606 (1979).
24. Pellegris, G.; Uleni. M.T.; Rovini. D.; Vaglini. M.; Cascinelli. N. and Ghidoni. A.: HLA complex and familial malignanl melanoma. Int. J. Cancer 29: 621-623 (1982).
25. Quinn, L.A.; Woods. L.K.; Merrick. S.B.; Arabasz. N.M., and Moore. G.E.: Cytogenetic analysis of twelve human malignant melanoma cell lines. J. natn. Cancer Inst. 59: 301-307 (1977).
26. Riccardi, V.M.; Sujansky. E.; Smith. A.C. and Francke, U.: Chromosomal imbalance in the aniridia-Wilms' tumor association: 11p interstitial deletion. Pediatrics 61: 604-610 (1978).
27. Rowley, J.D.: A new consisieni chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and Gicmsa staining. Nature. Lond. 243: 290-293 (1973a).
28. Rowley, J.D.: Identification of a Iranslocalion with quinacrine fluorescence in a patient With acute leukemia. Annis Génét. 16: 109-112 (1973).
29. Rowley, J.D.: Abnormalities of chromosome I in myeloproliferative disorders. Cancer 36: 1748-1757 (1975).
30. Semple, T.U.; Moore. G.E.; Morgan. R.T.; Woods. L.K. and Quinn. L.A.: Multiple cell lines from paiienis with malignant melanoma: morphology, karyology and biochemical analysis J. nam. Cancer Inst. 68:365-380 (1982).
31. Sutherland, C.M.; Kloepfer. H.W.; Mansell. P.W.A. and Kremeuiz. E.T.: Familial melanoma. In Pigment Cell (Proceedings of the 9th International Pigment Cell Conference). 2: 421-426 (1976).
32. Wallace, D.C.; Beardmore. G.L. and Exton. L.A.: Familial malignant melanoma. Ann. Surg. 177: 15-20 (1973).
33. Weitkamp, L. R. and Lamm. L. V.: Report of the committee on the genetic constitution of chromosome 6. In Human Gene Mapping 6 (1981): Sixth International Workshop on Human Gene Mapping. Birth Defects: Original Article Scries. Vol. 18. No. 2 (March of Dimes Birth Defects Foundation. While Plains, N.Y. 1982): also in Cytogenet. Cell Genet. 32: 111-120 (1982).
34. Whang-Peng, J.; Kao-Shan. C.S. Lee, E.C, Bunn. P.A.; Carney. D.N.; Gazdar. A. F. and Minna. J.D.: Specific chromosome defect associated with human small-cell lung cancer: deletion 3p (14-23). Science 215: 181-182 (1982).
35. Wilson, M.G.; Towner, J.W. and Fujimoto. A.: Retinoblastoma and D-chromosomc deletions. Am. J. hum. Genet. 25: 57-61 (1973).
36. Zankl, H. and Zang. K.D.: Cytological and cytogenetical studies on brain tumors. IV. Identification of the missing G chromosome in human meningiomas as No. 22 by fluorescence technique. Humangenetik 14: 167-169 (1972).
37. Zech, L.; Haglund, U.; Nilsson. K. and Klein. G.: Characteristic chromosomal abnormalities in biopsies and lymphoid cell lines from patients with Burkitt and non-Burkitt lymphomas. Int. J. Cancer 17: 47-56 (1976).