Fluorescent in situ hybridization (FISH) for the detection of trisomy 8 in acute myeloblastic leukemia

Leukemia and Lymphoma

Volumn 23, Issue 5-6, 1996, Pages 603-607

  Amiel, Aliza ^a   Elis, Avishay ^a   Manor, Yosef ^a   Tangi, Ilana ^a   Fejgin, Moshe ^a   Lishner, Michael ^a  

^a MEIR MEDICAL CENTER   (Israel)

Author keywords

Acute myeloblastic leukemia; AML; FISH; Trisomy 8

Indexed keywords

ACUTE MYELOBLASTIC LEUKEMIA; ADULT; AGED; ARTICLE; BLOOD DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; METAPHASE; PRIORITY JOURNAL; PROGNOSIS; TRISOMY 8;

EID: 0030447575     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.3109/10428199609054870     Document Type: Article

References (19)

1. Rowley, J. D. (1990) Recurring chromosome abnormalities in leukemia and lymphoma. Semin. Hematol., 27, 122-136.
2. Yunis, J. J., Brunning, R. D., Howe, R. B. and Lobell, M. (1984) High resolution chromosomes as an independent prognostic indicator in adult acute nonlymphocytic leukemia. N. Eng. J. Med., 311, 812-818.
3. Keating, M. J., Smith, T. L., Kantarjian, H., Cork, R., Walters, R., Trujillo, J. M , McCredie, B., Gehan, E. A. and Freireich, E. J. (1988) Cytogenetic pattern in acute myelogenous leukemia: A major reproducible determinant of outcome Leukemia, 2, 403-412.
4. Yunis, J. J. (1984) Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia. Cancer Genet. Cytogenet., 11, 125-137.
5. Walker, H., Smith, F. J. and Betts, D. R. (1994) Cytogenetics in acute myeloid leukemia. Blood Reviews, 8, 30-36.
6. Schiffer, C. A., Lee, E. T., Tomiyasu, T., Wiernik, P. H. and Testa, J. R. (1989) Prognostic impact of cytogenetic abnormalities in patients with denovo acute nonlymphocytic leukemia. Blood, 73, 263-270.
7. Stasi, R , Poeta, G., Masi, M., Tribalto, M., Venditti, A., Paper, G., Nicoletti, B., Vernole, P., Tedeschi, B , Delaroche, I., Mingairelli, R and Dollapiccola, B. (1993) Incidence of chromosome abnormalities and clinical significance of karyotype in denovo acute myeloid leukemia. Cancer Genet. Cytogenet , 67, 28-34.
8. Jenkins, R. B , LaBeau, M. M., Kraker, W. J , Borell, T. J., Stalborger, P. G., Davis, E. M , Penland, L., Fernuld, A., Espinosa, III R., Schaid, D. J., Noel, P. and DeWald, G. D. (1992) Fluorescent in situ hybridization: A sensitive method for trisomy 8 detection in bone marrow specimens. Blood, 79, 3307-3315.
9. McConnell, J. S., Duncan, M. H. and Foncar, K. (1991) Southwestern Oncology Group Leukemia Subcommittee. Do random (non-clonal) chromosome abnormalities in bone marrow predict a clone to come? Cancer Genet. Cytogenet, 53, 257-262.
10. Lalkin, A., Lishner, M., Gaber, E., Manor, Y., Fejgin, M., Ravid, M. and Amiel, A. (1993) In situ hybridization: A simple and sensitive method for detection of trisomy 12 in chronic lymphocytic leukemia. Cancer Genet. Cytogenet., 70, 21-24.
11. Amiel, A., Gaber, E., Manor, Y., Fejgin, M., Joseph-Lerner, N , Ravid, M. and Lishner, M. (1995) Fluorescent in situ hybridization for the detection of trisomy 8 and 9 in polycythemia vera. Cancer Genet. Cytogenet., 79, 153-156.
12. Anastasi, J., Le Beau, M. M., Vardiman, J. W., Fernald, A. A., Larson, E. A. and Rowley, J. D. (1992) Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescent in situ hybridization: a simple and sensitive method. Blood, 79, 1790-1801.
13. Rege-Cambrin, G., Mecucci, C., Tricot, G., Michanx, J. L., Louwagie, A., Van Hove, W., Francart, H. and Van den-Berghe, H. (1987) A chromosomal profile of polycythemia vera. Cancer Genet. Cytogenet., 25, 233-245.
14. Najean, Y., Deschamps, A., Dresch, C., Daniel, M. T., Rain, J. D. and Arrago, J. P. (1985) Acute leukemia and myelodysplasia in polycythemia vera. Cancer, 61, 89-95.
15. Diez-Martin, J. L., Graham, D. L., Petitt, R. M. and Dewald, G. W. (1991) Chromosome studies in 104 patients with polycythemia vera. Mayo Clin Proc., 66, 287-299.
16. Bagby, G. C. (1988) The preleukemic syndromes. Blood, 2, 194-205.
17. Hagenmeijer, A. (1987) Chromosome abnormalities in chronic myeloid leukemia. In: Bailliere's Clinical Hematology. Edited by Goldman JM. pp. 963-981. London: Bailliere Tindall.
18. Kibbelaar, R. E., Mulder, J. W. R., Dreef, E. J., Van Kamp, H., Fibbe, W. E., Wessels, J. W., Beverstock, G. C., Haak, H. L. and Kluin, M. (1993) Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: A comparison of banding and fluoresence in situ hybridization. Blood, 82, 904-913.
19. Kibbelaar, R. E., Van Kamp, H., Dreef, E J., Wessels, J. W., Beverstock, G. C., Roap, A. K., Fibbe, W E., Den Ottolander, G. J. and Kluin, PhM. (1991) Detection of trisomy 8 in hematological disorders by in situ hybridization. Cytogenet. Cell Genet., 56, 132-136.