Technical approach for the study of the genetic evolution of breast cancer from paraffin-embedded tissue sections

Breast Cancer Research and Treatment

Volumn 39, Issue 2, 1996, Pages 177-185

  Chen, Taiping ^a   Dhingra, Kapil ^b   Sahin, Aysegul ^b   Sneige, Nour ^b   Hortobagyri, Gabriel ^b   Aldaz, C Marcelo ^a  

^a UNIVERSITY OF TEXAS   (United States)

^b UNIVERSITY OF TEXAS   (United States)

Author keywords

Allelotype; Breast cancer; In situ hybridization; Paraffin sections

Indexed keywords

PARAFFIN;

ARTICLE; BREAST CANCER; BREAST CARCINOGENESIS; CANCER GENETICS; CHROMOSOME 17; CHROMOSOME ANALYSIS; DISSOCIATION; FEMALE; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; INTERPHASE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; TUMOR SUPPRESSOR GENE;

EID: 0029832277     PISSN: 01676806     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01806184     Document Type: Article

References (22)

1. Callahan R, Campbell G: Mutations in human breast cancer: an overview. J Natl Cancer Inst 81: 1780-1786, 1989
2. McGuire WL, Naylor SL: Loss of heterozygosity in breast cancer: cause or effect? J Natl Cancer Inst 81: 1764-1765, 1989
3. Chen-L-C, Kurisu W, Ljung BM, Goldman ES, Moore II D, Smith HS: Heterogeneity for allelic loss in human breast cancer. J Natl Cancer Inst 84: 506-510, 1992
4. Weber JL, May PE: Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J Hum Genet 44: 388-396, 1989
5. Futreal PA, Soderkvist P, Marks JR, Iglehart JD, Cochran C, Barrett JC, Wiseman RW: Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms. Cancer Res 52: 2624-2627, 1992
6. Jones MH, Nakamura Y: Deletion mapping of chromosome 3p in female genital tract malignancies using microsatellite polymorphism. Oncogene 7: 1631-1634, 1992
7. Aaltonen LA, Peltomäki P, Leach FS, Sistonen P, Pylkkänen L, Mecklin J-P, Järvinen H, Powell SM, Jen J, Hamilton SR, Petersen GM, Kinzler KW, Vogelstein B, de la Chappelle A: Clues to the pathogenesis of familial colorectal cancer. Science 260: 812-816, 1993
8. Hopman AHN, Moesker O, Smeets AWGB, Pauwels RP, Vooijs GP, Ramaekers FC: Numerical chromosome 1, 7, 9 and 11 aberrations in bladder cancer detected by in situ hybridization. Cancer Res 51: 644-651, 1991
9. Devilee P, Thierry RF, Kievits T, Kolluri R, Hopman AHN, Willard HF, Pearson PL, Cornelisse CJ: Detection of chromosome aneuploidy in interphase nucleic from human primary breast tumors using chromosome-specific repetitive DNA probes. Cancer Res 58: 5825-5830, 1988
10. Emmerich P, Jauch A, Hofmann M-C, Cremer T, Walt H: Interphase cytogenetics in paraffin embedded sections from human testicular germ cell tumor xenografts and in corresponding cultured cells. Laboratory Investigation 61: 235-242, 1989
11. Walt H, Emmerich P, Cremer T, Hofmann M-C, Bannwart F: Supernumerary chromosome 1 in interphase nuclei of atypical germ cells in paraffin-embedded human seminiferous tubules. Laboratory Investigation 61: 527-531, 1989
12. Dhingra K, Sahin A, Supak J, Kin SY, Hortobagyi G, Hittelman WN: Chromosome in situ hybridization on formalin-fixed mammary tissue using non-isotopic, non-fluorescent probes: technical considerations and biological implications. Breast Cancer Res and Treatment 23: 201-210, 1992
13. Oliphant AR, Wright EC, Swensen J, Gruis NA, Goldgar D, Skolnick MH: Dinucleotide repeat polymorphism at the D17S513 locus. Nucleic Acids Res 19: 4794, 1991
14. Hall JM, Friedman L, Guenther C, Lee MK, Weber JL, Black DM, King MC: Closing in on a breast cancer gene on chromosome 17q. Am J Hum Genet 50: 1235-1242, 1992
15. Polymeropoulos MH, Xiao H, Rath DS, Merril CR: Dinucleotide repeat polymorphism at the human gene of the light and heavy chains of myeloperoxidase glycoprotein (MPO). Nucleic Acids Res 19: 1961, 1991
16. Weissenhach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M: A second-generation linkage map of the human genome. Nature 359: 794-801, 1992
17. Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA, Tunnacliffe A: Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13: 718-725, 1992
18. Orita M, Iwahana H, Kanazawa H, Hayashi K, Seklye T: Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphism. Proc Natl Acad Sci USA 86: 2766-2770, 1989
19. Dhingra K, Sneige N, Pandita TK, Johnston DA, Lee JS, Emami K, Hortobagyi GN, Hittelman WN: Quantitative analysis of chromosome in situ hybridization signal in paraffin-embedded tissue sections. Cytometry 16: 100-112, 1994
20. O'Connell P, Pekkel V, Fuqua S, Osborne CK, Allred DC: Molecular genetic studies of early breast cancer evolution. Breast Cancer Research Treatment 32: 5-12, 1994
21. Radford DM, Fair K, Thompson AM, Ritter JH, Holt M, Steinbrueck T, Wallace M, Wells SA, Donis-Keller HR: Allelic loss on chromosome 17 in ductal carcinoma in situ of the breast. Cancer Res 53: 2947-2950, 1993
22. Deng G, Chen L-C, Schott DR, Thor A, Bhargava V, Ljung B-M, Chew K, Smith HS: Loss of heterozygosity and p53 gene mutations in breast cancer. Cancer Research 54: 499-505, 1994