Cell lineage specific involvement in acute promyelocytic leukaemia (APL) using a combination of May-Grunwald-Giemsa staining and fluorescence in situ hybridization techniques for the detection of the translocation t(15;17)(q22;q12)

British Journal of Haematology

Volumn 103, Issue 1, 1998, Pages 93-99

  Haferlach, Torsten ^a   Löffler, Helmut ^b   Nickenig, Christina ^b   Ramm Petersen, Lotte ^b   Meeder, Marlies ^b   Schoch, Robert ^b   Schlegelberger, Brigitte ^b   Schnittger, Susanne ^a   Schoch, Claudia ^a   Hiddemann, Wolfgang ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF KIEL   (Germany)

Author keywords

Acute promyelocytic leukaemia; Cell lineage involvement; FICTION; MGG and FISH

Indexed keywords

CD19 ANTIGEN; CD3 ANTIGEN; CD34 ANTIGEN;

ACUTE MYELOBLASTIC LEUKEMIA; ADULT; AGED; ANTIGEN EXPRESSION; ARTICLE; CELL LINE; CHROMOSOME TRANSLOCATION 15; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE REARRANGEMENT; GIEMSA STAIN; HUMAN; HUMAN CELL; IMMUNOPHENOTYPING; MALE; PRIORITY JOURNAL;

ADULT; AGED; AZURE STAINS; CELL LINEAGE; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; IMMUNOPHENOTYPING; IN SITU HYBRIDIZATION, FLUORESCENCE; LEUKEMIA, PROMYELOCYTIC, ACUTE; MALE; MIDDLE AGED; TRANSLOCATION, GENETIC;

EID: 7844251185     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1998.00959.x     Document Type: Article

References (30)

1. Bennett, J.M., Catovsky, D., Daniel, M.-T., Flandrin, G., Galton, D.A.G., Gralnick, H.R. & Sultan, C. (1976) Proposals for the classification of the acute leukaemias. British Joural of Haematology, 33, 451-458.
2. Bennett, J.M., Catovsky, D., Daniel, M.-T., Flandrin, G., Galton, D.A.G., Gralnick, H.R. & Sultan, C. (1980) A variant form of acute hypergranular promyelocytic leukaemia (M3). British Journal of Haematology, 44, 169-170.
3. Bennett, J.M., Catovsky, D., Daniel, M.-T., Flandrin, G., Galton, D.A.G., Gralnick, H.R. & Sultan, C. (1985) Proposed revised criteria for the classification of acute myeloid leukemia: a report of the French-American-British Cooperative Group. Annals of Internal Medicine, 103, 626-629.
4. Bernell, P., Arvidsson, I., Hast, R., Jacobsson, B. & Stenke, L. (1997) Differences in cell lineage involvement between MDS-AML and de novo AML studied by fluorescence in situ hybridization in combination with morphology. European Journal of Haematology, 58, 241-245.
5. Biondi, A., Rambaldi, A., Pandolli, P.P., Rossi, V., Giudici, G., Alcalay, M., Lo Coco, F., Diverio, D., Pogliani, E.M., Lanzi, E.M., Mandelli, F., Masera, G., Barbui, T. & Pelicci, P.G. (1992) Molecular monitoring of the myl/retinoic acid receptor-alpha fusion gene in acute promyelocytic leukemia by polymerase chain reaction. Blood, 80, 492-497.
6. Borrow, J., Goddard, A.D., Gibbons, B., Katz, F., Swirsky, D., Fioretos, T., Dube, I., Winfield, D., Kingston, J., Hagemeijer, A., Rees, J.K.H., Lister, T.A. & Solomon, E. (1992) Diagnosis of acute promyelocytic leukaemia by RT-PCR: detection of PML-RARA and RARA-PML fusion transcripts. British Journal of Haematology, 82, 529-540.
7. Chen, Z., Morgan, R., Stone, J.F. & Sandberg, A.A. (1994) Identification of complex t(15:17) in APL by FISH. Cancer Genetics and Cytogenetics, 72, 73-74.
8. + subpopulations. Blood, 86, 1139-1147.
9. Haferlach, T., Winkemann, M., Löffler, H., Schoch, R., Gassmann, W., Fonatsch, C., Schoch, C., Poetsch, M., Weber-Matthiesen, K. & Schlegelberger, B. (1996) The abnormal eosinophils are part of the leukemic cell population in AML M4Eo and carry the pericentric inversion 16: a combination of May-Grünwald-Giemsa staining and fluorescence in situ hybridization. Blood, 87, 2459-2463.
10. Haferlach, T., Winkemann, M., Nickenig, C., Meeder, M., Ramm-Petersen, L., Schoch, R., Nickelsen, M., Weber-Matthiesen, K., Schlegelberger, B., Schoch, C., Gassmann, W. & Löffler, H. (1997a) Which compartments are involved in Philadelphia-chromosome positive chronic myeloid leukaemia? An answer at the single cell level by combining May-Grünwald-Giemsa staining and fluorescence in situ hybridization techniques. British Journal of Haematology, 97, 99-106.
11. Haferlach, T., Winkemann, M., Ramm-Petersen, L., Meeder, M., Schoch, R., Weber-Matthiesen, K., Schlegelberger, B., Schoch, C., Ludwig, W.-D., Hiddemann, W. & Löffler, H. (1997b) New insights into the biology of Philadelphia-chromosome-positive acute lymphoblastic leukaemia using a combination of May-Grünwald-Giemsa staining and fluorescence in situ hybridization techniques at the single cell level. British Journal of Haematology, 99, 452-459.
12. ISCN (1995) An International System for Human Cytogenetic Nomenclature (ed. by F. Mitelman). Karger, Basel.
13. Keinänen, M., Griffin, J.D., Bloomfield, C.D., Machnicki, J. & de la Chapelle, A. (1988) Clonal chromosomal abnormalities showing multi-cell-lineage involvement in acute myeloid leukemia. New England Journal of Medicine, 318, 1153-1158.
14. Knuutila, S. (1997) Lineage specificity in haematological neoplasms. British Journal of Haematology, 96, 2-11.
15. Knuutila, S., Majander, P. & Ruutu, T. (1994a) 8;21 and 15;17 translocations: abnormalities in a single cell lineage in acute myeloid leukemia. Acta Haematoloaica, 92, 88-90.
16. Knuutila, S., Teerenhovi, L., Larramendy, M.L., Elonen, E., Franssila, K.O., Nylund, S.J., Timonen, T., Heinonen, K., Mahlamäki, E., Winqvist, R. & Ruutu, T. (1994b) Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms. Genes, Chromosomes and Cancer, 10, 95-102.
17. Lengfelder, E., Reichert, A., Hehlmann, R., Löffler, H., Fonatsch, C., Schoch, C., Staib, P., Seifarth, W., Sauerland, M.C., Heinecke, A., Wörmann, B., Hiddemann, W. & Büchner, T. (1997) Effects of high dose cytarabin (HD-ara-C) as part of double induction strategy in acute promyelocytic leukemia (APL) and results of combination with all-trans retinoic acid (ATRA). Blood, 90, 330a.
18. Löffler, H. (1991) Zytochemische Methoden. Praktische Blutzelldiagnostik (ed. by I. Boll and S. Heller), p. 187. Berlin.
19. Ludwig, W.-D., Teichmann, J.V. & Thiel, E. (1991) Immunzytologie. Praktische Blutzelldiagnostik (ed. by I. Boll and S. Heller), p. 212. Berlin.
20. Naoe, T., Kudo, K., Yoshida, H., Horibe, K. & Ohno, R. (1997) Molecular analysis of the t(15:17) translocation in de novo and secondary acute promyelocytic leukemia. Leukemia, 11, 287-288.
21. Paietta, E., Andersen, J., Gallagher, R., Bennett, J.M., Yunis, J., Cassileth, P., Rowe, J. & Wiernik, P.H. (1994) The immunophenotype of acute promyelocytic leukemia (APL): an ECOG study. Leukemia, 8, 1108-1112.
22. Rowley, J.D., Colomb, H.M. & Dougherty, C. (1977) 15;17 translocation: a consistent chromosomal change in acute promyelocytic leukaemia. Lancet, i, 549-550.
23. Schad, C.R., Hanson, C.A., Paietta, E., Casper, J., Jalal, S.M. & Dewald, G.W. (1994) Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemia. Mayo Clinic Proceedings, 69, 1047-1053.
24. Schoch, R., Jenisch, S., Haferlach, T., Müller-Ruchholtz, W., Gassmann, W. & Löffler, H. (1996) Glass slide smears are a suitable source for RT-PCR-based analysis of chromosomal aberrations in leukaemias. British Journal of Haematology, 92, 140-142.
25. Takatsuki, H., Sadamura, S., Umemura, T., Abe, Y., Goto, T., Yufu, Y., Katsuno, M., Hirata, J., Nishimura, J. & Nawata, H. (1993) PML/ RARA fusion gene is expressed in both granuloid/macrophage and erythroid colonies in acute promyelocytic leukaemia. British Journal of Haematology, 85, 477-482.
26. Turhan, A.G., Lemoine, F.M., Debert, C., Bonnet, M.L., Baillou, C., Picard, F., Macintyre, E.A. & Varet, B. (1995) Highly purified primitive hematopoietic stem cells are PML-RARA negative and generate nonclonal progenitors in acute promyelocytic leukemia. Blood, 85, 2154-2161.
27. van Lom, K., Hagemeijer, A., Vandekerckhove, F., de Greef, G.E., Sacchi, N. & Löwenberg, B. (1997) Clonality analysis of hematopoietic cell lineages in acute myeloid leukemia and translocation (8;21): only the myeloid cells are part of the malignant clone. Leukemia, 11, 202-205.
28. Vyas, R.C., Frankel, S.R., Agbor, P., Miller, W.H., Jr, Warrell, R.P., Jr & Hittelman, W.N. (1996) Probing the pathobiology of response to all-trans retinoic acid in acute promyelocytic leukemia: Premature chromosome condensation/fluorescence in situ hybridization analysis. Blood, 87, 218-226.
29. + Hodgkin and Reed-Sternberg cells in 100% of analysed cases of Hodgkins disease. Blood, 86, 1464-1468.
30. Weber-Matthiesen, K., Winkemann, M., Müller-Hermelink, A., Schlegelberger, B. & Grote, W. (1992) Simultaneous fluorescence immunophenotyping and interphase cytogenetics: a contribution to the characterization of tumor cells. Journal of Histochemistry and Cytochemistry, 40, 171-175.