Instability of chromosomes 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization

Cancer Genetics and Cytogenetics

Volumn 88, Issue 1, 1996, Pages 1-7

  Anamthawat Jónsson, Kesara ^a   Eyfjörd, Jórunn E ^b   Ögmundsdöttir, Helga M ^b   Pétursdóttir, Ingibjörg ^b   Steinarsdóttir, Margrét ^c  

^a Agricultural Research Institute Reykjavik   (Iceland)

^b ICELANDIC CANCER SOCIETY   (Iceland)

^c UNIVERSITY OF ICELAND   (Iceland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CARCINOMA; CHROMOSOME 1; CHROMOSOME 16; CHROMOSOME 17; CHROMOSOME 3; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOME LOSS; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INTERPHASE; KARYOTYPE; METAPHASE CHROMOSOME; PRIORITY JOURNAL;

EID: 0342313449     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(95)00203-0     Document Type: Article

References (20)

1. Hainsworth PJ, Garson OM (1990): Breast cancer cytogenetics and beyond. Aust N Z J Surg 60:327-336.
2. Gray JW, Pinkel D (1992): Molecular cytogenetics in human cancer diagnosis. Cancer 69:1539-1542.
3. Buckle VJ, Kearney L (1994): New methods in cytogenetics. Current Opn Genet Dev 4:374-382.
4. Berger R (1993) Non-radioactive in situ hybridization to metaphase and interphase nuclei of malignant cells. In: Sumner AT, Chandley AC (eds.): Chromosomes Today, vol. 11. Chapman & Hall, London. ISBN 0 412 47670 3, pp. 171-180.
5. Devilee P, Thierry RF, Kievits T, Kolluri R, Hopman AHN, Willard HF, Pearson PL, Cornelisse CJ (1988): Detection of chromosome aneuploidy in interphase nuclei from primary breast tumors using chromosome specific repetitive DNA probes. Cancer Res 48:5825-5830.
6. Kallioneimi A, Kallioniemi O-P, Sudar D, Rutovitz D, Gray JW, Waldman F, Dinkel D (1992): Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821.
7. Steinarsdóttir M, Snorradóttir S, Pétursdóttir I, Eyfjörd JE, Ögmundsdóttir HM (1995): Cytogenetic studies of breast carcinomas: different karyotypic profiles detected by direct harvesting and short term culture. Genes Chrom Cancer 13:239-248.
8. Manuelidis L (1985): Individual interphase chromosome domains revealed by in situ hybridization. Hum Genet 71:288-293.
9. Pandis N, Jin Y, Gorunova L, Petersson C, Bardi G, Idvall I, Johansson B, Ingvar C, Mamdahl N, Mitelman F, Heim S (1995): Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups. Genes Chrom Cancer 12:173-185.
10. Dutrillaux B, Gerbault-Seureau M, Zafrani B (1990): Characterization of chromosomal anomalies in human breast cancer. Cancer Genet Cytogenet 49:203-217.
11. Rodgers CS, Hill SM, Hultén MA (1984): Cytogenetic analysis in human breast carcinoma. I. Nine cases in the diploid range investigated using direct preparations. Cancer Genet Cytogenet 13:95-119.
12. Pandis N, Jin Y, Limon J, Bardi G, Idvall I, Mandahl N, Mitelman F, Heim S (1993): Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast. Genes Chrom Cancer 6:151-155.
13. Lu Y-J, Xiao S, Yan Y-S, Fu S-B, Liu Q-Z, Li P (1993): Direct chromosome analysis of 50 primary breast carcinomas. Cancer Genet Cytogenet 69:91-99.
14. Mitchell ELD, Santibanez-Koref MF (1990): 1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer. Genes Chrom Cancer 2:278-289.
15. Hall JM, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, King M-C (1990): Linkage of early-onset familial breast cancer to chromosome 17q12-q21. Science 250:684-689.
16. Slamon DJ, Godophin W, Jones LA, Holt JA, Wong SG, Keith SE, Levin WJ, Stuart SG, Udove J, Ullrich A, Press MF (1989): Studies of the HER-2 neu protooncogene in human breast and ovarian cancer. Science 244:707-712.
17. Maikin D, Li FP, Strong LC, Fraumeni JF, Nelson CE, Kim DH, Kassel J, Gryka MA, Bischoff FZ, Tiansky MA, Friend SH (1990): Germ-line p53 mutations in a familial syndrome of breast cancer, sarcomas and other neoplasms. Science 250: 1233-1238.
18. Thorlacius S, Börresen A-L, Eyfjörd JE (1993): Somatic p53 mutations in human breast carcinomas in an Icelandic population: a prognostic factor. Cancer Res 53:1637-1641.
19. Eyfjörd JE, Thoflacius S, Steinarsdóttir M, Valgardsdóttir R, Ögmundsdóttir HM, Anamthawat-Jónsson K (1995): P53 abnormalities and genomic instability in primary breast carcinomas. Cancer Res 25:646-651.
20. Dauwerse JG, Wiegant J, Raap AK, Breuning MH, van Ommen GJB (1992): Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype. Hum Mol Genet 1:593-598.