Detection of deletions in the short arm of chromosome 3 in uncultured renal cell carcinomas by interphase cytogenetics

Journal of Urology

Volumn 160, Issue 2, 1998, Pages 534-539

  Siebert, Reiner ^a   Jacobi, Christine ^a   Matthiesen, Peter ^a   Zuhlke Jenisch, Reina ^a   Potratz, Claudia ^a   Zhang, Yanming ^a   Stockle, Michael ^a   Kloppel, Gunter ^a   Grote, Werner ^a   Schlegelberger, Brigitte ^a  

^a UNIVERSITY OF KIEL   (Germany)

Author keywords

Chromosome 3; Deletion; In situ hybridization; Kidney neoplasms

Indexed keywords

ARTICLE; CHROMOSOME 3P; CHROMOSOME DELETION; CLEAR CELL CARCINOMA; CYTOGENETICS; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DIFFERENTIAL DIAGNOSIS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INTERPHASE; KIDNEY CARCINOMA; MONOSOMY; PRIORITY JOURNAL;

EID: 0032323035     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-5347(01)62954-9     Document Type: Article

References (25)

1. Thoenes, W., Störkel, S. and Rumpelt, H. J.: Histopathology and classification of renal cell tumors. Path. Res. Pract., 181: 125, 1995.
2. Murphy, W. M., Beckwith, J. B. and Farrow, G. M.: Tumors of the kidney, bladder and related urinary structures. In: Atlas of Tumor Pathology, Third series, Fascicle 11. American Registry of Pathology. Armed Forces Institute of Pathology: Washington, 1994.
3. Steiner, G. and Sidransky, D.: Molecular differential diagnosis of renal carcinoma. Am. J. Pathol., 149: 1791, 1996.
4. Van den Berg, E., Dijkhuizen, T., Osterhuis, J. W., Van Kessel, A. G., de Jong, B. and Störkel, S.: Cytogenetic classification of renal cell cancer. Cancer Genet. Cytogenet., 95: 103, 1997.
5. Bugert, P. and Kovacs, G.: Molecular differential diagnosis of renal cell carcinomas by microsatellite analysis. Am. J. Pathol., 149: 2081, 1996.
6. Corless, C. L., Aburatani, H., Fletcher, J. A., Housman, D. E., Amin, M. B. and Weinberg, D. S.: Papillary renal cell carcinoma: quantitation of chromosomes 7 and 17 by FISH, analysis of chromosome 3p for LOH, and DNA ploidy. Diagn. Mol. Pathol., 5: 53, 1996.
7. Beck, J. L., Hopman, A. H., Feitz, W. F., Schalken, J., Schaafsma, H. E., Van de Kaa C. A., Ramaekers, F. C., Hanselaar, A. G. and De Wilde, P. C.: Numerical aberrations of chromosomes 1 and 7 in renal cell carcinomas as detected by interphase cytogenetics. J. Pathol., 176: 123, 1995.
8. el-Naggar, A. K., Hurr, K., Tu, Z. N., Tucker, S. L., Swanson, D. and Hsu, P. H.: Interphase cytogenetics of renal cortical neoplasms. Correlation with DNA ploidy by flow cytometry. Am. J. Clin. Pathol., 104: 141, 1995.
9. Brown, J. A., Anderl, K. L., Borell, T. J., Qian, J., Bostwick, D. G. and Jenkins, R. B.: Simultaneous chromosome 7 and 17 gain and sex chromosome loss provide evidence that renal metanephric adenoma is related to papillary renal cell carcinoma. J. Urol., 158: 370-374, 1997.
10. Decker, H. J. H., Klauck, S. M., Lawrence, J. B., McNeil, J., Smith, D., Gemmill, R. M., Sandberg, A. A., Neumann, H. H. P., Simon, B., Green, J. and Seizinger, B. R.: Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL). Cancer Genet. Cytogenet., 77: 1, 1994.
11. Van den Berg, A. and Buys, C. H. C. M.: Involvement of multiple loci in chromosome 3 in renal cell cancer development. Genes Chrom. Cancer, 19: 59, 1997.
12. Van den Berg, A., Dijkhuizen, T., Draaijers, T. G., Hulsbeek, M. M. F., Maher, E. R., van den Berg, E., Störkel, S. and Buys, C. H. C. M.: Analysis of multiple renal cell adenomas and carcinomas suggests allelic loss at 3p21 to be a prerequisite for malignant development. Genes Chrom. Cancer, 19: 228, 1997.
13. Kok, K., Naylor, S. L. and Buys, C. H. C. M.: Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes. Adv. Cancer Res., 71: 27, 1997.
14. Gemmill, R. M., Chumakov, I., Scott, P., Waggoner, B., Rigault, P., Cypser, J., Chen, Q., Weissenbach, J., Gardiner, K., Wang, H., Pakarsky, Y., Le Gall, I., Le Paslier, D., Guillou, S., Li, E., Robinson, L., Hahner, L., Todd, S., Cohen, D. and Drabkin, H. A.: A second-generation YAC contig map of human chromosome 3. Nature, 377: 299, 1995.
15. Michaelis, S. C., Bardenheuer, W., Lux, A., Schramm, A., Gockel, A., Siebert, R., Willers, C., Schmidtke, K., Todt, B., van der Hout, A. H., Buys, C. H. C. M., Heppell-Parton, A. C., Rabbitts, P. H., Ungar, S., Smith, D., LePaslier, D., Cohen, D., Opalka, B. and Schütte, J.: Characterization and chromosomal assignment of yeast artificial chromosomes containing human 3p13-p21-specific sequence tagged sites. Cancer Genet. Cytogenet., 81: 1, 1995.
16. Bardenheuer, W., Michaelis, S., Lux, A., Vieten, L., Bröcker, F., Jülicher, K., Willers, C., Siebert, R., Smith, D. I., van der Hout, A. H., Buys, C., Schütte, J. and Opalka, B.: Construction of a consistent YAC contig for human chromosome region 3p14.1. Genome Res., 6: 176, 1996.
17. Poetsch, M., Weber-Matthiesen, K., Plendl, H. J., Grote, W. and Schlegelberger, B.: Detection of the t(14;18) chromosomal translocation by interphase cytogenetics with yeast-artificial-chromosome probes in follicular lymphoma and nonneoplastic lymphoproliferation. J. Clin. Oncol., 14: 963, 1996.
18. Stilgenbauer, S., Döhner, H., Bulgay-Mörschel, M., Weits, S., Bentz, M. and Lichter, P.: High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood, 81: 2118, 1993.
19. Sanchez, Y., El-Naggar, A., Pathak, S. and McNeill Killary, A.: A tumor suppressor locus within 3p14-p12 mediates rapid cell death of renal cell carcinoma in vivo. Proc. Natl. Acad. Sci., 91: 3383, 1994.
20. Shridhar, V., Wang, L., Rosati, R., Paradee, W., Shridhar, R., Mullins, C., Sakr, W., Grignon, D., Miller, O. J., Sun, Q. C., Petros, J. and Smith, D. I.: Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas. Oncogene, 14: 1269, 1997.
21. Wilke, C. M., Hall, B. K., Hoge, A., Paradee, W., Smith, D. I. and Glover, T. W.: FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites. Hum. Mol. Genet., 5: 187, 1996.
22. Wilhelm, M., Bugert, P., Kenck, C., Staehler, G. and Kovacs, G.: Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: a breakpoint cluster between loci D3S1285 and D3S1603. Cancer Res., 55: 5383, 1995.
23. Bugert, P., Kenck, C., Wilhelm, M. and Kovacs, G.: Refining a proximal breakpoint cluster at chromosome 3p11.2 in nonpapillary renal cell carcinomas. Int. J. Cancer, 68: 723, 1996.
24. Kovacs, G., Erlandsson, R., Boldog, F., Ingvarsson, S., Müller-Brechlin, R., Klein, G. and Sümeg, J.: Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc. Natl. Acad. Sci., 85: 1571, 1988.
25. Kovacs, G.: Molecular cytogenetics of renal cell tumors. Adv. Cancer Res., 62: 89, 1993.