Abstract
During the last decade strong evidence has been accumulated for a causal relationship between specific genetic alterations and the abnormal differentiation state and growth behaviour of malignant cells. Such alterations can be observed at different levels ranging from chromosome mutations to point mutations of certain genes and may arise in a given cell either spontaneously or due to the effect of mutagenic environmental factors.
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References
Alitalo K, Schwab M (1986) Oncogene amplification in tumor cells. In: Advances in Cancer Research. Academic Press, Orlando, Florida
Bellané-Chantelot C, Lacroix B, Ougen P, Billault A, Beaufils S, Bertrand S, Georges I, Glibert F, Gros I, Lucotte G, Susini L, Codani J-J, Gesnouin P, Pook S, Vaysseix G, Lu-Kuo J, Ried T, Ward D, Chumaskov I, Le Paslier D, Barrillot E, Cohen D (1992) Mapping the whole human genome ba fingerprinting yeast artificial chromosomes. Cell 70: 1059–1068
Caspersson T, Farber S, Foley GE, Kudynowski J, Modest EJ, Simonsson E, Wagh U, Zech L (1968) Chemical differentiation along metaphase chromosomes. Exp Cell Res 49: 219–226
Chumakov, I., Rigault, P., Guillou, S., Ougen, P., Billaut, A., Guasconi, G., Gervy, P., LeGall, I., Soularue, P., Grinas, L., Bougueleret, L., BellanneChantelot, C., Lacroix, B., Barillot, E., Gesnouin, P., Pook, S., Vaysseix, G., Frelat, G., Schmitz, A., Sambucy, J.-L., Bosch, A., Estivill, X., Weissenbach, J., Vignal, A., Riethman, H., Cox, D., Patterson, D., Gardiner, K., Hattori, M., Sakaki, Y., Ichikawa, H., Ohki, M., Le Paslier, D., Heilig, H., Antonarakis, S., and Cohen, D. (1992) Continuum of overlapping clones spanning the entire human chromosome 21q. Nature 359: 380–387
Collins S, Groudine M (1982) Amplification of endogeneous myc-related DNA sequences in a human myeloid leukaemia cell line. Nature 298: 679–681
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.
du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T (1993) Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet
Joos S, Scherthan H, Speicher MR, Schlegel J, Cremer T, Lichter P (1993) Detection of amplified DNA sequences by reserve chromosome painting using genomic tumor DNA as probe. Hum Genet.
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D (1992) Comparative genomic in situ hybridization for molecular cytogenetic analysis of solid tumors. Science 258: 818–821
Lengauer C, Green ED, Cremer T (1992a) Fluorescence in situ hybridization of YAC Clones after Alu-PCR Amplification. Genomics 13: 286–289
Lengauer C, Riethman HC, Speicher MR, Taniwaki M, Konecki D, Green ED, Becher R, Olson MV, Cremer T (1992b) Metaphase and interphase cytogenetics with Alu-PCR amplified YAC clones containing the BCR-gene and the protooncogenes c-raf-1, c-fms, c-erbB-2. Cancer Res 52: 2590–2596
Lengauer C, Speicher MR, Popp S, Jauch A, Taniwaki M, Ramaiah Nagaraja M, Riethman HC, Donis-Keller H, D’Urso M, Schlessinger D, Cremer T (1993) Chromosomal bar codes constructed by fluorescence in situ hybridization with multiple ALU-PCR products of multiple YAC clones. Submitted
Lichter P, Tang CJC, Call K, Hermanson G, Evans GA, Housman D, Ward DC (1990) High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science 247: 64–68
Nederlof PM, van der Flier S, Wiegant J, Raap AK, Tanke HJ, Ploem JS, van der Ploeg M (1990) Multiple fluorescence in situ hybridization. Cytometry 11: 126–131
Nederlof PM, van der Flier S, Vrolijk J, Tanke HJ, Raap AK (1992) Fluorescence ratio measurements of double-labeled probes for multiple in situ hybridization by digital imaging microscopy. Cytometry 13: 839–845
Ried T, Baldini A, Rand TC, Ward DC (1992a) Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy. Proc Natl Acad Sci USA 89: 1388–1392
Ried T, Lengauer C, Cremer T, Wiegant J, Raap AK, van der Ploeg M, Groitl P, Lipp M (1992b) Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization. Genes Chrom Cancer 4: 1–6
Rowley JD (1990) Molecular cytogenetics: Rosetta Stone for understanding Cancer-twenty-ninth GHA Clowes memorial award lecture. Cancer Research 50: 3816–3825
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© 1994 Springer-Verlag Berlin Heidelberg
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Cremer, T. et al. (1994). Detection of Genetic Imbalances in Tumor Genomes by Fluorescence in situ Hybridization with Tumor Genomic DNA and Subregional DNA Probes. In: Obe, G., Natarajan, A.T. (eds) Chromosomal Alterations. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78887-1_5
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DOI: https://doi.org/10.1007/978-3-642-78887-1_5
Publisher Name: Springer, Berlin, Heidelberg
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