Genetic progression, histological grade, and allelic loss in ductal carcinoma in situ of the breast

Cancer Research

Volumn 56, Issue 22, 1996, Pages 5260-5265

  Fujii, Hiroaki ^a   Szumel, Richard ^a,b   Marsh, Carla ^a   Zhou, Weibo ^a   Gabrielson, Edward ^a,c  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b GRADUATE HOSPITAL   (United States)

^c JOHNS HOPKINS BAYVIEW MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TUMOR MARKER;

ALLELE; ARTICLE; BREAST CARCINOMA; CANCER GRADING; CANCER INVASION; CARCINOMA IN SITU; CHROMOSOME LOSS; GENE MUTATION; GENETIC HETEROGENEITY; HISTOLOGY; HUMAN; HUMAN TISSUE; PRIORITY JOURNAL;

ALLELES; BREAST NEOPLASMS; CARCINOMA IN SITU; CARCINOMA, DUCTAL, BREAST; DISEASE PROGRESSION; DNA, NEOPLASM; DNA, SATELLITE; FEMALE; GENE DELETION; GENETIC MARKERS; HUMANS; POLYMERASE CHAIN REACTION;

EID: 0029803950     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. Tavassoli, F. A. Pathology of the Breast. Norwalk, CT Appleton & Lange, 1992.
2. Page, D. L., and Anderson, T. J. Diagnostic Histopathology of the Breast. New York: Churchill Livingston, 1987
3. Rosen, P. P., and Oberman, H. A. Tumors of the Mammary Gland Washington, DC: Armed Forces Institute of Pathology, 1993.
4. Page, D. L., Dupont, W. D., Rogers, L. W., and Landenberger, M. Intraductal carcinoma of the breast Follow-up after biopsy only. Cancer (Phila), 49: 751-758, 1982.
5. Schnitt, S. J., Silen, W., Sadowsky, N. L., Connolly, J. L., and Harris, J. R. Current concepts: ductal carcinoma in situ (intraductal carcinoma of the breast). N. Engl. J. Med., 318: 898-903, 1988.
6. Lagios, M. D., Margolin, F. R., Westdahl, P. R., and Rose, M. R. Mammographically detected ductal carcinoma in situ. Frequency of local recurrence following tylectomy and prognostic effect of nuclear grade on local recurrence. Cancer (Phila.), 63: 618-624, 1989
7. Fujii, H., Marsh, C., Cairns, P., Sidransky, D., and Gabrielson, E. Genetic divergence in the clonal evolution of breast cancer Cancer Res., 56: 1493-1497, 1996.
8. Fujii, H., Zhou, W., and Gabrielson, E. Detection of frequent allelic loss of 6q23-q25.2 in microdissected human breast cancer tissues Genes Chromosomes & Cancer, 16: 35-39, 1996.
9. Cairns, P., Polascik, T. J., Eby, Y., Tokino, K., Califano, J., Merlo, A., Mao, L., Heath, J., Jenkins, R., Westra, W., Rutter, J., Buckler, A., Gabrielson, E., Tockman, M., Cho, K. R., Hedrick, L., Bova, G. S., Isaacs, W., Koch, W., Schwab, D., and Sidransky, D. Frequency of homozygous deletion at p16/CDKN2 in primary human tumors Nat Genet., 11: 210-212, 1995.
10. Brenner, A. J., and Aldaz, C. M. Chromosome 9p allelic loss and p16/CDKN2 in breast cancer and evidence of p16 inactivation in immortal breast epithelial cells. Cancer Res., 55: 2892-2895, 1995.
11. Bieche, I., Champeme, M., Matifas, F., Cropps, C., Callahan, R., and Lindereau, R. Two distinct regions involved in 1p deletion in human primary breast cancer. Cancer Res., 53: 1990-1994, 1993.
12. Bieche, I., Champeme, M., and Lindereau, R. Loss and gain of distinct regions of chromosome 1q in primary breast cancer. Clin. Cancer Res., I: 123-127, 1995.
13. Borg, A., Zhang, Q. X., Olsson, H., and Wenngren, E. Chromosome 1 alterations in breast cancer: allelic loss on 1p and 1q is related to lymphogenic metastases and poor prognosis Genes Chromosomes & Cancer, 5: 311-320, 1992.
14. Takita, K-i., Sato, T., Miyagi, M., Watatani, M., Akiyama, F., Sakamoto, G., Kasumi, F., Abe, R., and Nakamura, Y. Correlation of loss of alleles on the short arms of chromosomes 11 and 17 with metastasis of primary breast cancer to lymph nodes. Cancer Res., 52: 3914-3917, 1992.
15. Negrini, M., Rasio, D., Hampton, G. M., Sabbioni, S., Rattan, S., Carter, S. L., Rosenberg, A. L., Schwartz, G. F., Shiloh, Y., Cavanee, W. K., and Croce, C. M. Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer identification of a new region at 11q23.3. Cancer Res., 55: 3003-3007, 1995.
16. Sato, T., Akiyama, F., Sakamoto, G., Kasumi, F., and Nakamura, Y. Accumulation of genetic alterations and progression of primary breast cancer. Cancer Res., 51: 5794-5799, 1991
17. Cropp, C. S., Lidereau, R., and Campbell, G. Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma, two additional regions identified. Proc. Natl. Acad. Sci., 87: 7737-7741, 1990.
18. Cropp, C., Champeme, M., Lidereau, R., and Callahan, R. Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted. Cancer Res., 53: 5617-5619, 1993.
19. Futreal, P. A., Soderkvist, P., Marks, J. R., Iglehart, J. D., Cochran, C., Barren, J. C., and Wiseman, R. W. Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms Cancer Res., 52: 2624-2627, 1992.
20. Andersen, T. I., Gaustad, A., Ottestad, L., Farrants, G. W., Nesland, J. M., Tveit, K. M., and Borresen, A. L. Genetic alterations of the tumour suppressor gene regions 3p, 11p, 13q, 17p, and 17q in human breast carcinomas. Genes Chromosomes & Cancer, 4: 113-121, 1992.
21. Tsuda, H., Callen, D. F., Fukutomi, T., Nakamura, Y., and Hirohaski, S. Allele loss on chromosome 16q24 2-qter occurs frequently in breast cancers irrespectively of differences in phenotype and extent of spread. Cancer Res., 54: 513-517, 1994
22. Dorion-Bonnet, F., Mautalen, S., Hostein, I.. and Longy, M. Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers. Genes Chromosomes & Cancer, 14: 171-181, 1995.
23. Schott, D. R., Chang, J. N., Deng, G., Kurisu, W., Kuo, W-L., Gray, J., and Smith, H. S. A candidate tumor suppressor gene in human breast cancers. Cancer Res., 54: 1393-1396, 1994.
24. Armitage, P., and Berry, G. Statistical Methods in Medical Research Oxford: Blackwell Scientific Publications, 1987.
25. Mashal, R. D., Morgan, J., and Sklar, J. Clonal analysis by study of X-chromosome inactivation in formalin-fixed paraffin-embedded tissue Cancer Res., 53: 4676-4679, 1993
26. Devilee, P., Schuuring, E., van de Vijver, M. J., and Cornelisse, C. J. Recent developments in the molecular genetic understanding of breast cancer. Crit. Rev Oncog., 5: 247-270, 1995.
27. Bieche, I., and Lidereau, R. Genetic alterations in breast cancer. Genes Chromosomes & Cancer 14: 227-251, 1995
28. O'Connell, P., Pekkel, V., Fuqua, S., Osborne, C. K., and Allred, D. C. Molecular genetic studies of early breast cancer evolution Breast Cancer Res. Treat., 32: 5-12, 1994
29. Tsuda, H., Fukutomi, T., and Hirohashi, S. Pattern of gene alterations in intraductal breast neoplasms associated with histological type and grade. Clin. Cancer Res., 1: 261-267, 1995
30. Radford, D. M., Fair, K. L., Phillips, N. J., Ritter, J. H., Steinbrueck, T., Holt, M. S., and Donis-Keller, H. Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p, and 17q. Cancer Res., 55: 3399-3405, 1995
31. Aldaz, C. M., Chen, T., Sahin, A., Cunningham, J., and Bondy, N. Comparative allelotype of in situ and invasive human breast cancer: high frequency of microsatellite instability in lobular breast carcinomas. Cancer Res., 55: 3976-3981, 1995.
32. Munn, K. E., Walker, R. A., Varley, J. M. Frequent alterations on chromosome 1 in ductal carcinoma in situ of the breast. Oncogene, 10: 1653-1657, 1995.
33. Zhuang, Z., Merino, M. J., Chuaqui, R., LIotta, L. A., and Emmert-Buck, M. R. Identical allelic loss on chromosome 11q13 in microdissected in situ and invasive breast cancer. Cancer Res., 55: 467-471, 1995.
34. Fearon, E. R., and Vogelstein, B. A. A genetic model for colorectal tumongenesis. Cell, 61: 759-767, 1990.