A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias

Genes Chromosomes and Cancer

Volumn 28, Issue 1, 2000, Pages 14-22

  Von Bergh, Anne ^a   Emanuel, Betty ^b   Van Zelderen Bhola, Shama ^a   Smetsers, Toon ^c   Van Soest, Ronald ^a   Stul, Michel ^b   Vranckx, Hilde ^b   Schuuring, Ed ^a   Hagemeijer, Anne ^b   Kluin, Philip ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ARTICLE; CHROMOSOME 11Q; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 11; CONTROLLED STUDY; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INTERMETHOD COMPARISON; MALE; PRIORITY JOURNAL; SOUTHERN BLOTTING;

ACUTE DISEASE; ADOLESCENT; ADULT; AGED; BACTERIOPHAGE P1; CHILD, PRESCHOOL; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 11; CLONING, MOLECULAR; CONTIG MAPPING; DNA PROBES; DNA-BINDING PROTEINS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; KARYOTYPING; LEUKEMIA; MALE; MIDDLE AGED; MYELOID-LYMPHOID LEUKEMIA PROTEIN; PROTO-ONCOGENES; TRANSCRIPTION FACTORS; TRANSLOCATION, GENETIC;

EID: 6744221199     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(200005)28:1<14::AID-GCC2>3.0.CO;2-X     Document Type: Article

References (30)

1. Akao Y, Seto M, Yamamoto K, Iida S, Nakazawa S, Inazawa J, Abe T, Takahashi T, Ueda R. 1992. The RCK gene associated with t(11;14) translocation is distinct from the MLL/ALL-1 gene with t(4;11) and t(11;19) translocations. Cancer Res 52:6083-6087.
2. Bain BJ, Moorman AV, Johansson B, Mehta AB, Seeker Walker LM. 1998. Myelodysplastic syndromes associated with 11q23 abnormalities. European 11q23 Workshop participants. Leukemia 12: 834-839.
3. Biondi A, Rambaldi A, Rossi V, Elia L, Caslini C, Basso G, Battista R, Barbui T, Mandelli F, Masera G, et al., 1993. Detection of ALL-1/AF4 fusion transcript by reverse transcription-polymerase chain reaction for diagnosis and monitoring of acute leukemias with the t(4;11) translocation. Blood 82:2943-2947.
4. Caligiuri MA, Strout MP, Oberkircher AR, Yu F, de la Chapelle A, Bloomfield CD. 1997. The partial tandem duplication of ALL1 in acute myeloid leukemia with normal cytogenetics or trisomy 11 is restricted to one chromosome. Proc Natl Acad Sci USA 94:3899-3902.
5. Caligiuri MA, Strout MP, Schichman SA, Mrozek K, Arthur DC, Herzig GP, Baer MR, Schiffer CA, Heinonen K, Knuutila S, Nousiainen T, Ruutu T, Block AW, Schulman P, Pedersen Bjergaard J, Croce CM, Bloomfield CD. 1996. Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with rrisomy 11. Cancer Res 56:1418-1425.
6. Chen SJ, Zelent A, Tong JH, Yu HQ, Wang ZY, Derre J, Berger R, Waxman S, Chen Z. 1993. Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia. J Clin Invest 91:2260-2267.
7. Cimino G, Lo Coco F, Biondi A, Elia L, Luciano A, Croce CM, Masera G, Mandelli F, Canaani E. 1993. ALL-1 gene at chromosome 11q23 is consistently altered in acute leukemia of early infancy. Blood 82:544-546.
8. de Boer CJ, Loyson S, Kluin PM, Kluin Nelemans HC, Schuuring E, van Krieken JH. 1993. Multiple breakpoints within the BCL-1 locus in B-cell lymphoma: Rearrangements of the cyclin D1 gene. Cancer Res 53:4148-4152.
9. de Greef GE, Hagemeijer A. 1996. Molecular and cytogenetic abnormalities in acute mycloid leukaemia and myelodysplastic syndromes. Baill Clin Haematol 9:1-18.
10. Djabali M, Selleri L, Parry P, Bower M, Young B, Evans GA. 1993. A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias. Nature Genet 2:113-118.
11. Grimwade D, Walker H, Oliver F, Wheatley K, Harrison C, Harrison G, Rees J, Hann I, Stevens R, Burnett A, Goldstone A on behalf of the Medical Research Council Adult and Children's Leukaemia Working Parties. 1998. The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1,612 patients entered into the MRC AML 10 Trial. Blood 92:2332-2333.
12. Gu Y, Nakamura T, Alder H, Prasad R, Canaani O, Cimino G, Croce CM, Canaani E. 1992. The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene. Cell 71:701-708.
13. Gu Y, Alder H, Nakamura T, Schichman SA, Prasad R, Canaani O, Saito H, Croce CM, Canaani E. 1994. Sequence analysis of the breakpoint cluster region in the ALL-1 gene involved in acute leukemia. Cancer Res 54:2326-2330.
14. Harbott J, Mancini M, Verellen Dumoulin C, Moorman AV, Secker Walker LM. 1998. Hematological malignancies with a deletion of 11q23: Cytogenctic and clinical aspects. European 11q23 Workshop participants. Leukemia 12:823-827.
15. Harrison CJ, Cuneo A, Clark R, Johansson B, Lafage Pochitaloff M, Mugneret F, Moorman AV, Secker Walker LM. 1998a. Ten novel 11q23 chromosomal partner sites. European 11q23 Workshop participants. Leukemia 12:811-822.
16. Harrison CJ, Seeker Walker LM. 1998b. The importance of cytogenetics and associated molecular techniques in the management of patients with leukaemia. Clin Oncol R Coll Radiol 10:255-261.
17. Hunger SP, Tkachuk DC, Amylon MD, Link MP, Carroll AJ, Welborn JL, Willman CL, Cleary ML. 1993. HRX involvement in de novo and secondary leukemias with diverse chromosome 11q23 abnormalities [see comments]. Blood 81:3197-3203.
18. Kobayashi H, Espinosa R, 3d, Thirman MJ, Fernald AA, Shannon K, Diaz MO, Le Beau MM, Rowley JD. 1993a. Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization. Genes Chromosomes Cancer 7:204-208.
19. Kobayashi H, Espinosa R, 3d, Thirman MJ, Gill HJ, Fernald AA, Diaz MO, Le Beau MM, Rowley JD. 1993b. Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization. Blood 82:547-551.
20. Martineau M, Berger R, Lillington DM, Moorman AV, Secker Walker LM. 1998. The t(6;11)(q27;q23) translocation in acute leukemia: a laboratory and clinical study of 30 cases. EU Concerted Action 11q23 Workshop participants. Leukemia 12:788-791.
21. Poirel H, Rack K, Delabesse E, Radford Weiss I, Troussard X, Debert C, Leboeuf D, Bastard C, Picard F, Veil Buzyn A, Flandrin G, Bernard O, Macintyre E. 1996. Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and MS. Blood 87:2496-2505.
22. Rowley JD. 1993. Rearrangements involving chromosome band 11Q23 in acute leukaemia. Semin Cancer Biol 4:377-385.
23. Rowley JD, Diaz MO, Espinosa R, 3d, Patel YD, van Melle E, Ziemin S, Taillon Miller P, Lichter P, Evans GA, Kersey JH, et al., 1990. Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome. Proc Natl Acad Sci USA 87:9358-9362.
24. Rowley JD, Reshmi S, Sobulo O, Musvee T, Anastasi J, Raimondi S, Schneider NR, Barredo JC, Cantu ES, Schlegelberger B, Behm F, Doggett NA, Borrow J, Zeleznik Le N. 1997. All patients with the t(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders. Blood 90: 535-541.
25. Sinclair PB, Green AR, Grace C, Nacheva EP. 1997. Improved sensitivity of BCR-ABL detection: a triple-probe three-color fluorescence in situ hybridization system. Blood 90:1395-1402.
26. Sorensen PH, Chen CS, Smith FO, Arthur DC, Domer PH, Bernstein ID, Korsmeyer SJ, Hammond GD, Kersey JH. 1994. Molecular rearrangements of the MLL gene are present in most cases of infant acute myeloid leukemia and are strongly correlated with monocytic or myelomonocytic phenotypes. J Clin Invest 93:429-437.
27. Strout MP, Marcucci G, Bloomfield CD, Caligiuri MA. 1998. The partial tandem duplication of ALL1 (MLL) is consistently generated by Alu-mediated homologous recombination in acute myeloid leukemia. Proc Natl Acad Sci USA 95:2390-2395.
28. Vaandrager JW, Schuuring E, Zwikstra E, de Boer CJ, Kleiverda KK, van Krieken JH, Kluin Nelemans HC, van Ommen GJ, Raap AK, Kluin PM. 1996. Direct visualization of dispersed 11q13 chromosomal translocations in mantle cell lymphoma by multicolor DNA fiber fluorescence in situ hybridization. Blood 88:1177-1182.
29. Yamamoto K, Seto M, Iida S, Komatsu H, Kamada N, Kojima S, Kodera Y, Nakazawa S, Saito H, Takahashi T, Ueda R. 1994. A reverse transcriptase-polymerase chain reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities. Blood 83:2912-2921.
30. Ziemin van der Poel S, McCabe NR, Gill HJ, Espinosa R, III, Patel Y, Harden A, Rubinelli P, Smith SD, Le Beau MM, Rowley JD, et al., 1991. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias [published erratum appears in Proc Natl Acad Sci USA 1992 (May 1);89:4220]. Proc Natl Acad Sci USA 88:10735-10739.