Detailed genome-wide screening for inter- and intrachromosomal abnormalities by sequential G-banding and RxFISH color banding of the same metaphase cells

Cancer Genetics and Cytogenetics

Volumn 119, Issue 2, 2000, Pages 94-101

  Teixeira, Manuel R ^a   Micci, Francesca ^a   Dietrich, Claudia U ^a   Heim, Sverre ^a  

^a INSTITUTE OF CANCER RESEARCH   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BONE MARROW CELL; CANCER; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HEMATOLOGIC DISEASE; HUMAN; MALE; MARKER CHROMOSOME; METAPHASE; METHODOLOGY; PRIORITY JOURNAL;

ADOLESCENT; AGED; ANEUPLOIDY; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN; FEMALE; GENOME; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; METAPHASE; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES; NEOPLASMS; SPECIMEN HANDLING;

EID: 0034091604     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00220-4     Document Type: Article

References (27)

1. Schröck E., du Manoir S., Veldman T., Schoell B., Wienberg J., Ferguson-Smith M.A., Ning Y., Ledbetter D.H., Bar-Am I., Soenksen D., Garini Y., Ried T. Multicolor spectral karyotyping of human chromosomes. Science. 273:1996;494-497.
2. Speicher M.R., Gwyn Ballard S., Ward D.C. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genet. 12:1996;368-375.
3. Müller S., O'Brien P.C., Ferguson-Smith M.A., Wienberg J. Cross-species colour segmenting. a novel tool in human karyotype analysis Cytometry. 33:1998;445-452.
4. Veldman T., Vignon C., Schröck E., Rowley J.D., Ried T. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping. Nature Genet. 15:1997;406-410.
5. Rao P.H., Cigudosa J.C., Ning Y., Calasanz M.J., Iida S., Tagawa S., Michaeli J., Klein B., Dalla-Favera R., Jhanwar S.C., Ried T., Chaganti R.S. Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma. Blood. 92:1998;1743-1748.
6. Sawyer J.R., Lukacs J.L., Munshi N., Desikan K.R., Singhal S., Mehta J., Siegel D., Shaughnessy J., Barlogie B. Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping. Blood. 92:1998;4269-4278.
7. Rowley J.D., Reshmi S., Carlson K., Roulston D. Spectral karyotype analysis of T-cell acute leukemia. Blood. 93:1999;2038-2042.
8. Teixeira M.R., Micci F., Dietrich C.U., Heim S. Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes. Genes Chromosom Cancer. 26:1999;13-19.
9. Micci F., Teixeira M.R., Dietrich C.U., Heim S. Combined RxFISH/G-banding allows refined karyotyping of solid tumors. Hum Genet. 104:1999;370-375.
10. Pandis N., Bardi G., Heim S. Interrelationship between methodological choices and conceptual models in solid tumor cytogenetics. Cancer Genet Cytogenet. 76:1994;77-84.
11. An International System for Human Cytogenetic Nomenclature. 1995;S. Karger, Basel.
12. Smit V.T., Wessels J.W., Mollevanger P., Schrier P.I., Raap A.K., Beverstock G.C., Cornelisse C.J. Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes. Cytogenet Cell Genet. 54:1990;20-23.
13. Babu V.R., Wiktor A. A fluorescence in situ hybridization technique for retrospective cytogenetic analysis. Cytogenet Cell Genet. 57:1991;16-17.
14. Dubinsky R., Amiel A., Manor Y., Radnay Y., Fejgin M., Ravid M., Lishner M. Fluorescence in situ hybridization (FISH) for retrospective detection of trisomies 3 and 7 in multiple myeloma. Cancer Genet Cytogenet. 83:1995;115-118.
15. Wiktor A., Puskorius R., Zubrickas K., Van Dyke D.L. Sequential G-banding and fluorescent in situ hybridization on peripheral blood, bone marrow, and amniotic fluid samples. Am J Med Genet. 79:1998;38-41.
16. Shi G., Weh H.J., Hossfeld D.K. Reinterpretation of G-banded complex karyotypes by fluorescence in situ hybridization with chromosome-specific DNA painting probes and alpha-satellite centromere-specific DNA probes in malignant hematological disorders. Am J Hematol. 55:1997;69-76.
17. Jalal S.M., Law M.E., Christensen E.R., Spurbeck J.L., Dewald G.W. Method for sequential staining of GTL-banded metaphases with fluorescent-labeled chromosome-specific paint probes. Am J Med Genet. 46:1993;98-103.
18. Zhao L., Hayes K., Glassman A. A simple efficient method of sequential G-banding and fluorescence in situ hybridization. Cancer Genet Cytogenet. 103:1998;62-64.
19. Colls P., Templado C., Martínez-Pasarell O., Darroudi F., Natarajan A.T. Sequential G-banding FISH on human sperm chromosomes. Chromosome Res. 5:1997;457-461.
20. Klever M., Grond-Ginsbach C., Scherthan H., Schroeder-Kurth T.M. Chromosomal in situ suppression hybridization after Giemsa banding. Hum Genet. 86:1991;484-486.
21. El-Rifai W., Knuutila S. Fluorescent in situ hybridization on archival G-banded slides. Cytogenet Cell Genet. 73:1996;322-324.
22. Liehr T., Kirsch M., Trautmann U., Gebhart E. Fluorescence in situ hybridization on G-banded chromosome preparations mounted with Eukitt in a retrospective study and in routine diagnostics. Cancer Genet Cytogenet. 107:1998;85-86.
23. Gerdes A.M., Pandis N., Bomme L., Dietrich C.U., Teixeira M.R., Bardi G., Heim S. Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations. Cancer Genet Cytogenet. 98:1997;9-15.
24. Mitelman F. Catalog of Chromosome Aberrations in Cancer, CD-ROM version 1. 1998;Wiley-Liss, New York.
25. Romana S.P., Le C.M., Berger R. t(12;21). a new recurrent translocation in acute lymphoblastic leukemia Genes Chromosom Cancer. 9:1994;186-191.
26. Romana S.P., Poirel H., Leconiat M., Flexor M.A., Mauchauffe M., Jonveaux P., Macintyre E.A., Berger R., Bernard O.A. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood. 86:1995;4263-4269.
27. Amor D.J., Algar E.M., Slater H.R., Smith P.J. High frequency of t(12;21) in childhood acute lymphoblastic leukemia detected by RT-PCR. Pathology. 30:1998;381-385.