Cytogenetic studies of tumor tissue from patients with nonfamilial renal cell carcinoma

Cancer Research

Volumn 46, Issue , 1986, Pages 2139-2147

  Yoshida, Mitsuaki A ^a   Ohyashiki, Kazuma ^a   Ochi, Hisako ^a   Gibas, Zenon ^a   Pontes, J Edson ^a   Huben, Robert ^a   Sandberg, Avery A ^a   Prout, George R ^b  

^a ROSWELL PARK CANCER INSTITUTE   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; CLINICAL ARTICLE; CYTOGENETICS; ETIOLOGY; HEREDITY; HUMAN; KIDNEY; KIDNEY CARCINOMA; PRIORITY JOURNAL;

ADULT; AGED; CARCINOMA, RENAL CELL; CHROMOSOME ABERRATIONS; FEMALE; HUMANS; KARYOTYPING; KIDNEY NEOPLASMS; MALE; METAPHASE; MIDDLE AGED; ONCOGENES; TRANSLOCATION, GENETIC;

EID: 0022647143     PISSN: 00085472     EISSN: 15387445     Source Type: Journal    
DOI: None     Document Type: Article

References (40)

1. Sandberg, A. A. The Chromosomes in Human Cancer and Leukemia. New York: Elsevier North-Holland, Inc., 1980.
2. Gibas, L. M., Gibas, Z., and Sandberg, A. A. Technical aspects of cytogenetic analysis of solid tumors. Karyogram, 10: 25-27, 1984.
3. Wake, N., Slocum, H. K., Rustum, Y. M., Matsui, S. I., and Sandberg, A. A. Chromosomes and causation of human cancer and leukemia. XLIV. A method for chromosome analysis of solid tumors. Cancer Genet. Cytogenet., 3: 1-10, 1981.
4. Whang-Peng, J., Bunn, P. A., Jr., Kao-Shan, C. S., Lee, E. C., Carney, D. N., Gazdar, A., and Minna, J. D. A nonrandom chromosomal abnormality, del 3p(14–23), in human small cell lung cancer (SCLC). Cancer Genet. Cytogenet., 6: 119-134, 1982.
5. Wake, N., Hreshchyshyn, M. M., Piver, S. M., Matsui, S. I., and Sandberg, A. A. Specific cytogenetic changes in ovarian cancer involving chromosomes 6 and 14. Cancer Res., 40: 4512-4518, 1980.
6. Kakati, S., Song, S. Y., and Sandberg, A. A. Chromosomes and causation of human cancer and leukemia. XXII. Karyotypic changes in malignant melanoma. Cancer (Phila.), 40: 1173-1181, 1977.
7. Pathak, S., Drwinga, H. L., and Hsu, T. C. Involvement of chromosome 6 in rearrangements in human malignant melanoma cell lines. Cytogenet. Cell Genet., 36: 573-579, 1983.
8. Quinn, L. A., Woods, L. K., Merrick, S. B., Arabass, N. M., and Moore, G. E. Cytogenetic analysis of human malignant melanoma cell lines. J. Natl. Cancer Inst., 59: 301-307, 1977.
9. Dayal, H., and Kinman, J. Epidemiology of kidney cancer. Semin. Oncol., 10: 366-377, 1983.
10. Cohen, A. J., Li, F. P., Berg, S., Marchetto, D. J., Tsai, S., Jacobs, S. C., and Brown, R. S. Hereditary renal-cell carcinoma associated with a chromosomal translocation. N. Engl. J. Med., 301: 592-595, 1979.
11. Pathak, S., Strong, L. C., Ferrell, R. E., and Trinidade, A. Familial renal cell carcinoma with a 31; 11 chromosome translocation limited to tumor cells. Science (Wash. DC), 217: 939-940, 1982.
12. Wang, N., and Perkins, K. L. Involvement of band 3pl4 in t(3;8) hereditary renal carcinoma. Cancer Genet. Cytogenet., 11: 479-481, 1984.
13. 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.
14. Wilson, M. G., Towner, J. W., and Fujimoto, A. Retinoblastoma and D-chromosome deletions. Am. J. Hum. Genet., 25: 57-61, 1973.
15. Kaneko, Y., Egues, M. C., and Rowley, J. D. Interstitial deletion of short arm of chromosome 11 limited to Wilms’ tumor cells in a patient without aniridia. Cancer Res., 41: 4577-4578, 1981.
16. Riccardi, V. M., Sujansky, E., Smith, A. C., and Francke, U. Chromosomal inbalance in the aniridia-Wilms’ tumor association: 11p interstitial deletion. Pediatrics, 61: 604-610, 1978.
17. Yoshida, M. C., Ikeuchi, T., and Sasaki, M. Differential staining of parental chromosomes in interspecific cell hybrids with a combined quinacrine and 33258 Hoechst technique. Proc. Jpn. Acad., 51: 184-187, 1975.
18. Yunis, J. J. New chromosome techniques in the study of human neoplasia. Hum. Pathol., 12: 540-549,1981.
19. Hagemeijer, A., Hoehn, W., and Smit, E. M. E. Cytogenetic analysis of human renal carcinoma cell lines of common origin (NC 65). Cancer Res., 39: 4662-4667, 1979.
20. Ferti-Passantonopoulou, A., Panani, A., and Raptsi, S. G-banded karyotype of a primary renal-cell carcinoma. Cancer Genet. Cytogenet., 11: 227–232, 1984.
21. Wang, N., Soldat, L., Fan, S., Figemshau, S., Clayman R., and Fraley, E. The consistent involvement of chromosome 3 and 6 aberrations in renal cell carcinoma. Am. J. Hum. Genet., 35: 73A, 1983.
22. Rowley, J. D. Human oncogene locations and chromosome aberrations. Nature (Lond.), 301: 290–291, 1983.
23. Yunis, J. J. The chromosomal basis of human neoplasia. Science (Wash. DC), 221: 227–236, 1983.
24. Adams, J. M., Gerondakis, S., Webb, E., Corcoran, L. M., and Cory, S. Cellular myc oncogene is altered by chromosome translocation to an immunoglobulin locus in murine plasmacytomas and is rearranged similarly in human Burkitt lymphomas. Proc. Natl. Acad. Sci. USA, 80: 1982–1986, 1983.
25. Dalla-Favera, R., Bregni, M., Erikson, J., Patterson, D., Gallo, R. C., and Croce, C. M. Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. Proc. Natl. Acad. Sci. USA, 79: 7824–7827, 1982.
26. Hayday, A. C., Gillies, S. D., Saito, H., Wood, C., Wiman, K., Hayward, W. S., and Tonegawa, S. Activation of a translocated human c-myc gene by an enhancer in the immunoglobulin heavy-chain locus. Nature (Lond.), 307: 334–340, 1984.
27. Taub, R., Kirsch, I., Morton, C., Lenoir, C., Swan, D., Tronick, S., Aaronson, S., and Leder, P. Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells. Proc. Natl. Acad. Sci. USA, 79: 7837-7841, 1982.
28. Cairns, J. The origin of human cancers. Nature (Lond.), 289: 353-357, 1981.
29. Klein, G. The roles of gene dosage and genetic transpositions in carcinogenesis. Nature (Lond.), 294: 313–318, 1981.
30. Slamon, D. J., deKernion, J. B., Verma, I. M., and Cline, M. J. Expression of cellular oncogene in human malignancies. Science (Wash. DC), 224: 256-262, 1984.
31. Hecht, F., and Sutherland, G. R. Fragile sites and cancer breakpoints. Cancer Genet. Cytogenet., 12: 179-181, 1984.
32. Yunis, J. J. Fragile sites and predisposition to leukemia and lymphoma. Cancer Genet. Cytogenet., 12: 85-88, 1984.
33. Yunis, J. J., and Soreng, A. L. Constitutive fragile sites and cancer. Science (Wash. DC), 226: 1199-1204, 1984.
34. Bonner, T. L., Rapp, U. R., Nash, W. G., and O’Brien, S. J. Two human homologs to a new retroviral oncogene raf-1 and raf-2 are assigned to human chromosomes 3 and 4, respectively. Cytogenet. Cell Genet., 37: 424, 1984.
35. Jhanwar, S. C., Neel, B. G., Hayward, W. S., and Chaganti, R. S. K. Localization of c-ras oncogene family on human germ-line chromosome. Proc. Natl. Acad. Sci. USA, 80: 4794-4797, 1983.
36. Cavenee, W. K., Dryja, T. P., Phillips, R. A., Benedict, W. F., Godbout, R., Gallie, B. L., Murphee, A. L., Strong, L. C., and White, R. L. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature (Lond.), 305: 779-784, 1983.
37. Fearon, E. R., Vogelstein, B., and Feinberg, A. P. Somatic deletion and duplication of genes on chromosome 11 in Wilms’ tumours. Nature (Lond.), 309: 176-178, 1984.
38. Koufos, A., Hansen, M. F., Lampkin, B. C., Workman, M. L., Copeland, N. G., Jenkins, N. A., and Cavenee, W. K. Loss of alleles at loci on human chromosome 11 during genesis of Wilms’ tumour. Nature (Lond.), 309: 170-172, 1984.
39. Orkin, S. H., Goldman, D. S., and Sallan, S. E. Development of homozygosity for chromosome 11p markers in Wilms’ tumour. Nature (Lond.), 309: 172–174, 1984.
40. Reeve, A. E., Housiaux, P. J., Gardner, R. J. M., Chewings, W. E., Grindley, R. M., and Millow, L. J. Loss of a Harvey ras allele in sporadic Wilms’ tumour. Nature (Lond.), 309:174-176, 1984. carcinoma. Am. J. Hum. Genet., 35: 73A, 1983.