Loss of Heterozygosity at 11q22-q23 in Breast Cancer

Cancer Research

Volumn 54, Issue 23, 1994, Pages 6270-6274

  Carter, Stephen L ^a   Negrini, Massimo ^a   Baffa, Raffaele ^a   Gillum, Diane R ^a   Rosenberg, Anne L ^a   Schwartz, Gordon F ^a   Croce, Carlo M ^a  

^a THOMAS JEFFERSON UNIVERSITY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; BREAST CARCINOGENESIS; CHROMOSOME 11Q; CHROMOSOME LOSS; GENE FREQUENCY; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ATAXIA TELANGIECTASIA; BREAST NEOPLASMS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 11; DNA, NEOPLASM; FEMALE; GENE AMPLIFICATION; HUMAN; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027945323     PISSN: 00085472     EISSN: 15387445     Source Type: Journal    
DOI: None     Document Type: Article

References (32)

1. Lasko, D., Cavenee, W., and Nordenskjold, M. Loss of constitutional heterozygosity in human cancer. Annu. Rev. Genet., 25: 281-314, 1991.
2. Genuardi, M., Tsihira, H., Anderson, D. E., and Sanders, G. F. Distal deletion of chromosome 1p in ductal carcinoma of the breast. Am. J. Hum. Genet., 45: 73-82, 1989.
3. Chen, L. C., Dollbaum, C., and Smith, H. Loss of heterozygosity on chromosome 1q in human breast cancer. Proc. Natl. Acad. Sci. USA, 86: 7204-7207, 1989.
4. Devilee, P., Van den Broek, M., Kuiper-Dijkshoorn, N., Kolluri, R., Meera Khan, P., Pearson, P. L., and Cornelisse, C. J. At least four different chromosomal regions are involved in loss of heterozygosity in human breast cancer. Genomics, 5: 554-560, 1989.
5. Devilee, P., van Vliet, M., van Sloun, P., Kuipers-Dijkshoorn, N., Hermans, J., Pearson, P. L., and Cornelisse, C. J. Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q. Oncogene, 6: 1705-1711, 1991.
6. Bieche, I., Champeme, C. H., Matifas, F., Hacene, K., Callahan, R., and Lidereau, R. Loss of heterozygosity on chromosome 7q and aggressive primary breast cancer. Lancet, 339: 139-143, 1992.
7. Ali, I. U., Lidereau, R., Theillet, C., and Callahan, R. Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia. Science (Washington DC), 238: 185-188, 1987.
8. Lundberg, C., Skoog, L., Cavenee, W. K., and Nordenskjold, M. Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13. Proc. Natl. Acad. Sci. USA, 84: 2372-2376, 1987.
9. Mackay, J., Steel, C. M., Elder, P. A., Forrest, A. P. M., and Evans, H. J. Allele loss on short arm of chromosome 17 in breast cancers. Lancet, 2: 1384-1385, 1988.
10. Futreal, P. A., Soderkvist, P., Marks, J. R., Iglehart, J. D., Cochran, C., Barrett, 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.
11. Devilee, P., van Vliet, M., van Sloun, P., Kuipers-Dijkshoora, N., Hermans, J., Pearson, P. L., and Cornelisse, C. J. Somatic genetic changes on chromosome 18 in breast carcinomas: is the DCC gene involved? Oncogene, 6: 311-315, 1991.
12. Ferti-Passantonopoulou, A., Panani, A. D., and Raptis, S. Preferential involvement of 11q23-24 and 11p15 in breast cancer. Cancer Genet. Cytogenet., 51: 183-188, 1991.
13. Negrini, M., Sabbioni, S., Possati, L., Rattan, S., Corallini, A., Barbanti-Brodano, G., and Croce, C. M. Suppression of tumorigenicity of breast cancer cells by microcell-mediated chromosome transfer: studies on chromosomes 6 and 11. Cancer Res., 54: 1331-1336, 1994.
14. Larsson, C., Skogseid, B., Oberg, K., Nakamura, Y., and Noerdenskjold, M. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature (Lond.), 332: 85-87, 1988.
15. Tomlinson, I. P. M., Gammack, A. J., Stickland, J. E., Mann, G. J., MacKie, R. M., Kefford, R. F., and McGee, J. O'D. Loss of heterozygosity in malignant melanoma at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers. Genes Chromosomes Cancer, 7: 169-172, 1993.
16. Foulkes, W. D., Campbell, I. G., Stamp, G. W., and Trowsdale, J. Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer. Br. J. Cancer, 67: 268-273, 1993.
17. Keldysh, P. L., Dragani, T. A., Fleischman, E. W., Konstantinove, L. N., Perevos-chikov, A. G., Pierotti, M. A., Della Porta, G., and Kopnin, B. P. 11q deletions in human colorectal carcinomas: cytogenetic and restriction fragment length polymorphism analysis. Genes Chromosomes Cancer, 6: 45-50, 1993.
18. Hampton, G. M., Penny, L. A., Baergen, R. N., Larson, A., Brewer, C., Liao, S., Busby-Earle, R. M. C., Williams, A. W. R., Steel, C. M., Bird, C. C., Stanbridge, E. J., and Evans, G. A. Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24. Proc. Natl. Acad. Sci. USA, 91: 6953-6957, 1994.
19. Winqvist, R., Mannermaa, A., Alavaikko, M., Blanco, G., Taskinen, P., Kiviniemi, I. N., and Cavenee, W. Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors. Cancer Res., 53: 4486-4488, 1993.
20. Maniatis, T., Fritsch, E. F., and Sambrook, J. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory, 1982.
21. Genome Data Base (GDB), Baltimore, MD: Johns Hopkins University, William H. Welch Library, 1994.
22. Gu, Y., Nakamuta, T., Alder, H., Prasad, R., Canaani, O., Cimino, G., Croce, C. M., and Canaani, E. The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene. Cell, 71: 701-708, 1992.
23. Dutrillaux, B., Gerbault-Seureau, M., and Zafrani, B. Characterization of chromosomal anomalies in human breast cancer. Cancer Genet. Cytogenet., 49: 203-217, 1990.
24. Stickland, J. E., Tomlinson, I. P. M., Lee, A. S. G., Evans, M. F., and McGee, J. O. Allelic loss on chromosome 11q is a frequent event in breast cancer. Br. J. Cancer, 66 (Suppl. XVII): 3, 1992.
25. Vogclstein, B., Fearon, E. R., Hamilton, S. R., Kern, S. E., Preisinger, A. C., Leppert, M., Nakamura, Y., White, R., Smits, A. M. M., and Bos, J. L. Genetic alterations during colorectal-tumor development. N. Engl. J. Med., 319: 525-532, 1988.
26. Nagayama, K., and Watatani, M. Analysis of genetic alterations related to the development and progression of breast cancer. Jpn. J. Cancer Res., 84: 1159-1164, 1993.
27. Sato, T., Tanigami, A., Yamakawa, K., Akiyama, F., Kasumi, F., Sakamoto, G., and Nakamura, Y. Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer. Cancer Res., 50: 7184-7189, 1990.
28. 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.
29. Swift, M., Morrell, D., Massey, R. B., and Chase, C. L. Incidence of cancer in 161 families affected by ataxia-telangiectasia. N. Engl. J. Med., 325: 1831-1836, 1991.
30. Cortessis, B., Ingles, S., Millikan, R., Diep, A., Gatti, R. A., Richardson, L., Thompson, W. D., Paganini-Hill, A., Sparkes, R. S., and Haile, R. W. Linkage analysis of DRD2, a marker linked to the ataxia-telangiectasia gene, in 64 families with premenopausal bilateral breast cancer. Cancer Res., 53: 5083-5086, 1993.
31. Wooster, R., Ford, D., Mangian, J., Ponder, B. A., Pcto, J., Easton, D. F., and Stratton, M. R. Absence of linkage to the ataxia-telangiectasia locus in familial breast cancer. Hum. Genet., 92: 91-94, 1993.
32. Hampton, G. M., Mannermaa, A., Winquist, R., Alavaikko, M., Blanco, G., Taskinen, P. J., Kiviniemi, H., Newsham, I., Cavenee, W. K., and Evans, G. A. Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3. Cancer Res., 54: 4586-4589, 1994.