Chromosome translocations in breast cancer with breakpoints at 8p12

Genomics

Volumn 66, Issue 1, 2000, Pages 15-25

  Courtay Cahen, Celine ^a   Morris, Joanna S ^a   Edwards, Paul A W ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; CHROMOSOME BREAKAGE; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; GENE AMPLIFICATION; GENE DELETION; GENE MAPPING; HUMAN; PRIORITY JOURNAL; TELOMERE;

EID: 0034657347     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6178     Document Type: Article

References (48)

1. Adelaide J., Chaffanet M., Imbert A., Allione F., Geneix J., Popovici C., van Alewijk D., Trapman J., Zeillinger R., Borresen-Dale A.-L., Lidereau R., Birnbaum D., Pebusque M.-J. Chromosome region 8p11-p21: Refined mapping and molecular alterations in breast cancer. Genes Chromosomes Cancer. 22:1998;186-199.
2. Albertsen H. M., Abderrahim H., Cann H. M., Dausset J., Le Paslier D., Cohen D. Construction and characterization of a yeast artificial chromosome library containing seven haploid genome equivalents. Proc. Natl. Acad. Sci. USA. 87:1990;4256-4260.
3. Bautista S., Theillet C. CCND1 and FGFR1 coamplification results in the colocalisation of 11q13 and 8p12 sequences in breast tumor nuclei. Genes Chromosomes Cancer. 22:1998;268-277.
4. Bernardino J., Apiou F., Gerbault-Seureau M., Malfoy B., Dutrillaux B. Characterization of recurrent homogeneously staining regions in 72 breast carcinomas. Genes Chromosomes Cancer. 23:1998;100-108.
5. Carter N. P., Ferguson-Smith M. A., Perryman M. T., Telenius H., Pelmear A. H., Leversha M. A., Glancy M. T., Wood S. L., Cook K., Dyson H. M., Ferguson-Smith M. E., Willatt M. R. Reverse chromosome painting: A method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. J. Med. Genet. 29:1992;299-307.
6. Chaffanet M., Popovici C., Imbert A., Samson D., Birnbaum D., Pebusque M.-J. Novel sequence tagged sites from the human 8p12-p21 chromosomal region involved in breast cancer. Oncol. Rep. 4:1997;367-369.
7. Chumakov I. M., Rigault P., Le Gall I., Bellanné-Chantelot C., Billault A., Guillou S., Soularue P., Guasconi G., Poullier E., Gros I., Belova M., Sambucy J.-L., Susini L., Gervy P., Glibert F., Beaufils S., Bui H., Massart C., De Tand M.-F., Dukasz F., Lecoulant S., Ougen P., Perrot V., Saumier M., Soravito C., Bahouayila R., Cohen-Akenine A., Cohen D. A YAC contig map of the human genome. Nature. 377:1995;175-297.
8. Coquelle A., Toledo F., Stern S., Bieth A., Debatisse M. A new role for hypoxia in tumour progression: Induction of fragile site triggering genome rearrangements and formation of complex DMs and HSRs. Mol. Cell. 2:1998;259-265.
9. Courjal F., Cuny M., Simony-Lafontaine J., Louason G., Speiser P., Zeillinger R., Rodriguez C., Theillet C. Mapping of DNA amplifications at 15 chromosomal localisations in 1875 breast tumors: Definition of phenotypic groups. Cancer Res. 57:1997;4360-4367.
10. Dib A., Adelaide J., Chaffanet M., Imbert A., Le Paslier D., Jacquemier J., Gaudray P., Theillet C., Birnbaum D., Pebusque M.-J. Characterisation of the region of the short arm of chromosome 8 amplified in breast cancer. Oncogene. 10:1995;995-1001.
11. Dutrillaux B. Pathways of chromosome alteration in human epithelial cancers. Adv. Cancer Res. 67:1995;59-82.
12. Dutrillaux B., Gerbault-Seureau M., Zafrani B. Characterisation of chromosomal anomalies in human breast cancer. A comparison of 30 paradiploid cases with few chromosome changes. Cancer Genet. Cytogenet. 49:1990;203-217.
13. Engel L. W., Young N. A., Tralka T. S., Lippman M. E., O'Brien S. J., Joyce M. J. Establishment and characterisation of three new continuous cell lines derived from human breast carcinomas. Cancer Res. 38:1978;3352-3364.
14. Gosden C. M., Davidson C., Robertson M. Lymphocyte culture. Ronney D. E., Czepulkowski B. H. Human Cytogenetics. 1992;IRL Press, Oxford.
15. Guan X.-Y., Meltzer P. S., Dalton W. S., Trent J. M. Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection. Nat. Genet. 8:1994;155-161.
16. Huang H., Qian J., Proffit J., Wilber K., Jenkins R., Smith D. FRA7G extends over a broad region: Coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites. Oncogene. 16:1998;2311-2319.
17. Hudson T. J. An STS-based map of the human genome. Science. 270:1995;1945-1954.
18. Ioannou P. A., de Jong P. J. Construction of bacterial artificial chromosome libraries using the modified P1 (PAC) system. Dracopoli. Current Protocols in Human Genetics. 1996;Wiley, New York.
19. James L. A., Mitchell E. L. D., Menasce L., Varley J. M. Comparative genomic hybridisation of ductal carcinoma in situ of the breast: Identification of regions of DNA amplification and deletion in common with invasive breast carcinoma. Oncogene. 14:1997;1059-1065.
20. Jin Y., Jin C., Wennerberg J., Mertens F., Hoglund M. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13. Cancer Res. 58:1998;5859-5865.
21. Keydar I., Chen L., Karby S., Weiss F. R., Delarea J., Radu M., Chaitcik S., Brenner H. J. Establishment and characterisation of a cell line of human breast carcinoma origin. Eur. J. Cancer. 15:1979;659-670.
22. Levy A., Dang U.-C., Bookstein R. High-density screen of human tumour cell lines for homozygous deletions of loci on chromosome arm 8p. Genes Chromosomes Cancer. 24:1999;42-47.
23. Lin C. C., Sasi R., Lee C., Fan Y. S., Court D. Isolation and identification of a tandemly repeated DNA sequence in the centromeric region of human chromosome 8. Chromosoma. 102:1993;333-339.
24. Martins C., Jin Y., Jin C., Wennerberg J., Hoglund M., Mertens F. Fluorescent in situ hybridisation (FISH) characterisation of pericentromeric breakpoints on chromosome 5 in head and neck squamous cell carcinomas. Eur. J. Cancer. 35:1999;498-501.
25. Mathias N., Bayes M., Tyler-Smith C. Highly informative compound haplotypes for the human Y chromosome. Hum. Mol. Genet. 3:1994;115-123.
26. Morris J. S., Carter N. P., Ferguson-Smith M. A., Edwards P. A. W. Cytogenetic analysis of three breast carcinoma cell lines using reverse chromosome painting. Genes Chromosomes Cancer. 20:1997;120-139.
27. Muleris M., Salmon R. J., Dutrillaux B. Existence of two distinct processes of chromosomal evolution in near-diploid colorectal tumors. Cancer Genet. Cytogenet. 32:1988;43-50.
28. Muleris M., Almeida A., Gerbault-Seureau M., Malfoy B., Dutrillaux B. Identification of amplified DNA sequences in breast cancer and their organisation within homogeneously staining regions. Genes Chromosomes Cancer. 14:1995;155-163.
29. Nishizaki T., De Vries S., Chew K., Goodson W. H. III, Ljung B.-M., Thor A., Waldman F. M. Genetic alterations in primary breast cancers and their metastases: Direct comparison using modified comparative genomic hybridisation. Genes Chromosomes Cancer. 19:1997;267-272.
30. Pandis N., Jin Y., Gorunova L., Petersson C., Bardi G., Idvall I., Johansson B., Ingvar C., Mandahl N., Mitelman F., Heim S. Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups. Genes Chromosomes Cancer. 12:1995;173-185.
31. Parada L. A., Hallen M., Tranberg K.-G., Hagerstrand I., Bondeson L., Mitelman F., Johansson B. Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer. Genes Chromosomes Cancer. 23:1998;26-35.
32. Paradee W., Wilkie C. M., Wang L., Shridhar R., Mullins C. M., Hoge A., Glover T. W., Smith D. I. A 350 kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints. Genomics. 35:1996;87-93.
33. Prasad M. A., Trybus T. M., Wojno K. J., Macoska J. A. Homozygous and frequent deletion of proximal 8p sequences in human prostate cancers: Identification of a potential tumor suppressor gene site. Genes Chromosomes Cancer. 23:1998;255-262.
34. Saint-Ruf C., Gerbault-Seureau M., Viegas-Pequignot E., Zafrani B., Malfoy B., Dutrillaux B. Recurrent homogeneously staining regions in 8p1 in breast cancer and lack of amplification of POLB, LHRH, and PLAT genes. Cancer Genet. Cytogenet. 52:1991;27-35.
35. Satya-Prakash K. L., Pathak S., Hsu T. C., Olive M., Cailleau R. Cytogenetic analysis on eight human breast tumor cell lines: High frequencies of 1q, 11q, and HeLa-like marker chromosomes. Cancer Genet. Cytogenet. 3:1981;61-73.
36. Schuler G. D. A gene map of the human genome. Science. 274:1996;540-546.
37. Schwab M. Amplification of oncogenes in human cancer cells. BioEssays. 20:1998;473-479.
38. Seitz S., Rohde K., Bender E., Nothnagel A., Kolble K., Schlag P. M., Scherneck S. Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: Linkage analysis in German breast cancer families. Oncogene. 14:1997;741-743.
39. Smedley D., Hamoudi R., Clark J., Warren W., Abdul-Rauf M., Somers G., Venter D., Fagan K., Cooper C., Shipley J. The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP. Human Mol. Genet. 7:1998;637-642.
40. Sunwoo J. B., Holt M. S., Radford D. M., Deeker C., Scholnick S. B. Evidence for multiple tumor suppressor genes on chromosome arm 8p in supraglottic laryngeal cancer. Genes Chromosomes Cancer. 16:1996;164-169.
41. Sutherland G. R., Richards R. I. The molecular basis of fragile sites in human chromosomes. Curr. Opin. Genet. Dev. 5:1995;323-327.
42. Takle L. A., Knowles M. A. Deletion mapping indicates two tumour suppressor genes on chromosome 8p in the development of bladder cancer. Oncogene. 12:1996;1083-1087.
43. Thompson F., Emerson J., Dalton W., Yang J.-M., McGee D., Villar H., Knox S., Massey K., Weinstein R., Bhattacharyya A., Trent J. Clonal chromosome abnormalities in human breast carcinomas. I. Twenty-eight cases with primary disease. Genes Chromosomes Cancer. 7:1993;185-193.
44. Tirkkonen M., Tanner M., Karhu R., Kallioniemi A., Isola J., Kallioniemi O. Molecular cytogenetics of primary breast cancer by CGH. Genes Chromosomes Cancer. 21:1998;177-184.
45. van Alewijk D. C., van der Weiden M. M., Eussen B. J., van den Andel-Thijssen L. D., Ehren-van Eekelen C. C., Konig J. J., van Steenbrugge G. J., Dinjens W. N., Trapman J. Identification of a homozygous deletion at 8p12-21 in a human prostate cancer xenograft. Genes Chromosomes Cancer. 24:1999;119-126.
46. Wang X.-Z., Jolicoeur E. M., Conte M., Chaffanet M., Zhang Y., Mozziconacci M.-J., Feiner H., Birnbaum D., Pebusque M.-J., Ron D. γ-Heregulin is the product of a chromosomal translocation fusing the DOC4 and HGL/NRG1 genes in the MDA-MB-175 breast cancer cell line. Oncogene. 18:1999;5718-5721.
47. Wright K., Wilson P. J., Kerr J., Do K., Hurst T., Khoo S.-K., Ward B., Chenevix-Trench G. Frequent loss of heterozygosity and three critical regions on the short arm of chromosome 8 in ovarian adenocarcinomas. Oncogene. 17:1998;1185-1188.
48. Yaremko M. L., Kutza C., Lyzak J., Mick R., Recant W. M., Westbrook C. A. Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behaviour in breast cancer. Genes Chromosomes Cancer. 16:1996;189-195.