Fluorescence in situ hybridization analysis of renal oncocytoma reveals frequent loss of chromosomes Y and 1

Journal of Urology

Volumn 156, Issue 1, 1996, Pages 31-35

  Brown, James A ^a   Takahashi, Satoru ^a   Alcaraz, Antonio ^a   Borell, Thomas J ^a   Anderl, Kari L ^a   Qian, Junqi ^a   Persons, Diane L ^a   Bostwick, David G ^a   Lieber, Michael M ^a   Jenkins, Robert B ^a  

^a MAYO CLINIC   (United States)

Author keywords

chromosomes; in situ hybridization, fluorescence; kidney neoplasms

Indexed keywords

ARTICLE; CHROMOSOME 1; CHROMOSOME ANALYSIS; CHROMOSOME LOSS; CYTOGENETICS; FLOW CYTOMETRY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; METAPHASE; ONCOCYTOMA; PRIORITY JOURNAL; TISSUE SECTION; Y CHROMOSOME;

EID: 8944261602     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-5347(01)65929-9     Document Type: Article

References (32)

1. Lieber, M. M. and Tsukamoto, T.: Renal oncocytoma. In: Tumors of the Kidney. Edited by J. B. deKernion and M. Pavone-Macaluso. Baltimore: Williams & Wilkins, pp. 306-309, 1986.
2. Davidson, A. J., Hayes, W. S., Hartman, D. S., McCarthy, W. F. and Davis, C. J., Jr.: Renal oncocytoma and carcinoma: failure of differentiation with CT. Radiology, 186: 693, 1993.
3. Rainwater, L. M., Farrow, G. M. and Lieber, M. M.: Flow cytometry of renal oncocytoma: common occurrence of deoxyribonucleic acid polyploidy and aneuploidy. J. Urol., 135: 1167, 1986.
4. Hartwick, R. W., El-Naggar, A. K., Ro, J. Y., Srigley, J. R., McLemore, D. D., Jones, E. C., Grignon, D. J., Thomas, M. J. and Ayala, A. G.: Renal oncocytoma and granular renal cell carcinoma. A comparative clinicopathologic and DNA flow cytometric study. Amer. J. Clin. Path., 98: 587, 1992.
5. Wolf, J. S., Jr. and Carroll, P. R.: Bilateral renal oncocytoma: management and nuclear analysis. J. Surg. Oncol., 48: 272, 1991.
6. Psihramis, K. E. and Goldberg, S. D.: Flow cytometric analysis of cellular deoxyribonucleic acid content of nine renal oncocytomas. Urology, 38: 310, 1991.
7. Eble, J. N. and Sledge, G.: Cellular DNA content of renal oncocytomas: flow cytometric analysis of paraffin-embedded tissue from eight tumors. J. Urol., 136: 522, 1986.
8. Jow, W. W., Zeid, M. Y., Cowan, D., Malin, B. and Deberry, J. L., III: Renal oncocytoma: long-term follow-up and flow cytometric analysis. J. Surg. Oncol., 46: 53, 1991.
9. Zbar, B., Brauch, H., Talmadge, C. and Linehan, M.: Loss of alleles of foci on the short arm of chromosome 3 in renal cell carcinoma. Nature, 327: 721, 1987.
10. Kovacs, G., Erlandsson, R., Boldog, F., Invargsson, S., Müller-Brechlin, R., Klein, G. and Sümergi, S.: Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc. Natl. Acad. Sci., 85: 1571, 1988.
11. Kovacs, G. and Frisch, S.: Clonal chromosome abnormalities in tumor cells from patients with sporadic renal cell carcinoma. Cancer Res., 49: 651, 1989.
12. Dobin, S. M., Harris, C. P., Reynold, J. A., Coffield, K. S., Klugo, R. C., Peterson, R. F. and Speights, V. O.: Cytogenetic abnormalities in renal oncocytic neoplasms. Genes Chrom. Cancer, 4: 25, 1992.
13. Psihramis, K. E., Althausen, A. F., Yoshida, M. A., Prout, G. R., Jr. and Sandberg, A. A.: Chromosome anomalies suggestive of malignant transformation in bilateral renal oncocytoma. J. Urol., 136: 892, 1986.
14. Koss, L. G., Czerniak, B., Herz, F. and Wersto, R. P.: Flow cytometric measurements of DNA and other cell components in human tumors: a critical appraisal. Hum. Path., 20: 528, 1989.
15. Crotty, T. B., Lawrence, K. M., Moertel, C. A., Bartelt, D. H., Jr., Batts, K. P., Dewald, G. W., Farrow, G. M. and Jenkins, R. B.: Cytogenetic analysis of six renal oncocytomas and a chromophobe cell renal carcinoma. Evidence that -Y, -1 may be a characteristic anomaly in renal oncocytomas. Cancer Genet. Cytogenet, 61: 61, 1992.
16. Meloni, A. M., Sandberg, A. A. and White, R. D.: -Y,-1 as recurrent anomaly in oncocytoma. Letter to the Editor. Cancer Genet. Cytogenet., 61: 108, 1992.
17. Alcaraz, A., Takahashi, S., Brown, J. A., Herath, J. F., Bergstralh, E. J., Larson-Keller, J. J., Lieber, M. M. and Jenkins, R. B.: Aneuploidy and aneusomy of chromosome 7 detected by fluorescence in situ hybridization are markers of poor prognosis in prostate cancer. Cancer Res., 54: 3998, 1994.
18. Brown, J. A., Alcaraz, A., Takahashi, S., Persons, D. L., Lieber, M. M. and Jenkins, R. B.: Chromosomal aneusomies detected by fluorescent in situ hybridization analysis in clinically localized prostate carcinoma. J. Urol., 152: 1157, 1994.
19. Takahashi, S., Qian, J., Brown, J. A., Alcaraz, A., Bostwick, D. G., Lieber, M. M. and Jenkins, R. B.: Potential markers of prostate cancer aggressiveness detected by fluorescence in situ hybridization in needle biopsies. Cancer Res., 54: 3574, 1994.
20. Koss, L. G., Czerniak, B., Herz, F. and Wersto, R. P.: Flow cytometric measurements of DNA and other cell components in human tumors: a critical appraisal. Hum. Path., 20: 528, 1989.
21. Craig-Holmes, A. P., Moore, F. B. and Shaw, M. W.: Polymorphism of human C-band heterochromatin I. Frequency of variants. Amer. J. Hum. Genet., 25: 181, 1973.
22. Buckton, K. E., O'Riordan, M. L., Jacobs, P. A., Robinson, J. A., Hill, R. and Evans, H. J.: C- and Q-band polymorphism in the chromosomes of three human populations. Ann. Hum. Genet., 40: 99, 1976.
23. Cher, M. L., MacGrogan, D., Bookstein, R., Brown, J. A., Jenkins, R. B. and Jensen, R. H.: Comparative genomic hybridization, allelic imbalance, and fluorescence in situ hybridization on chromosome 8 in prostate cancer. Genes Chrom. Cancer, 11: 153, 1994.
24. Bruns, G. A. and Dracopoli, N. C.: HGM11: report of the committee on the genetic constitution of chromosome 1. Cytogenet. Cell Genet., 58: 103, 1991.
25. Mitelman, F., Kaneko, Y. and Trent, J.: Report of the committee on chromosome changes in neoplasia. Cytogenet. Cell Genet., 55: 358, 1990.
26. Seizinger, B. R., Klinger, H. P., Junien, C., Nakamura, Y., Le Beau, M., Cavenee, W., Emanuel, B., Ponder, B., Naylor, S., Mitelman, F., Louis, D., Menon, A., Newsham, I., Decker, J., Kaelbling, M., Henry, I. and von Deimling, A.: HGM11: report of the committee on chromosome and gene loss in human neoplasia. Cytogenet. Cell Genet., 58: 1080, 1991.
27. Manuel, M., Katayama, K. P. and Jones, H. W., Jr.: The age of occurence of gonad tumors in intersex patients with a Y chromosome. Amer. J. Obst. Gynec., 124: 293, 1976.
28. Sultana, R., Myerson, D. and Disteche, C. M.: In situ hybridization analysis of the Y chromosome in gonadoblastoma. Genes Chrom. Cancer, 13: 257, 1995.
29. Lundgren, R., Mandahl, N., Heim, S., Limon, J., Henrikson, H. and Mitelman, F.: Cytogenetic analysis of 57 primary prostatic adenocarcinomas. Genes Chrom. Cancer, 4: 16, 1992.
30. Heim, S.: Cytogenetics in the investigation of haematological disorders. Bailleres Clin. Haematol., 3: 921, 1990.
31. Walter, T. A., Berger, C. S. and Sandberg, A. A.: The cytogenetics of renal tumors. Where do we stand, where do we go? Cancer Genet. Cytogenet., 43: 15, 1989.
32. Bigner, S. H., Mark, J. and Bigner, D. D.: Cytogenetics of human brain tumors. Cancer Genet. Cytogenet., 47: 141, 1990.