Chromosome abnormalities and MLL rearrangements in acute myeloid leukemia of infants

Leukemia

Volumn 13, Issue 7, 1999, Pages 1013-1017

  Satake, N ^a   Maseki, N ^a   Nishiyama, M ^a   Kobayashi, H ^a   Sakurai, M ^a   Inaba, H ^b   Katano, N ^c   Horikoshi, Y ^d   Eguchi, H ^e   Miyake, M ^f   Seto, M ^g   Kaneko, Y ^a  

^a SAITAMA CANCER CENTER   (Japan)

^b MIE UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c AICHI UNIVERSITY   (Japan)

^d SHIZUOKA CHILDREN'S HOSPITAL   (Japan)

^e KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f OSAKA MEDICAL COLLEGE   (Japan)

^g AICHI CANCER CENTER HOSPITAL   (Japan)

Author keywords

11q23 translocations; Infant acute myeloid leukemia; MLL gene

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; CANCER SURVIVAL; CHILDHOOD LEUKEMIA; CHROMOSOME 11Q; CHROMOSOME 12P; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; CLASSIFICATION; CLINICAL ARTICLE; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE REARRANGEMENT; HUMAN; INFANT; INTRON; KARYOTYPE; MALE; PRIORITY JOURNAL; PROGNOSIS; TREATMENT OUTCOME;

EID: 0032814043     PISSN: 08876924     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.leu.2401439     Document Type: Article

References (34)

1. Kaneko Y, Shikano T, Maseki N, Sakurai Ma, Sakurai Mi, Takeda T, Hiyoshi Y, Mimaya J, Fujimoto T. Clinical characteristics of infant acute leukemia with or without 11q23 translocations. Leukemia 1988; 2: 672-676.
2. Bernard OA, Berger R. Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations. Genes Chromosomes Cancer 1995; 13: 75-85.
3. Greaves MF. Infant leukemia biology, aetiology and treatment. Leukemia 1996; 10: 372-377.
4. Chen C-S, Sorensen PHB, Domer PH, Reaman GH, Korsmeyer SJ, Heerema NA, Hammond GD, Kersey JH. Molecular rearrangements on chromosome 11q23 predominate in infant acute lymphoblastic leukemia and are associated with specific biologic variables and poor outcome. Blood 1993; 81: 2386-2393.
5. Rubnitz JE, Link MP, Shuster JJ, Carroll AJ, Hakami N, Frankel LS, Pullen DJ, Cleary ML. Frequency and prognostic significance of HRX rearrangements in infant acute lymphoblastic leukemia: a pediatric oncology group study. Blood 1994; 84: 570-573.
6. Cimino G, Rapanotti MC, Rivolta A, Coco FL, D'Arcangelo E, Rondelli R, Basso G, Barisone E, Rosanda C, Santostasi T, Canaani E, Masera G, Mandelli F, Biondi A. Prognostic relevance of ALL-1 gene rearrangement in infant acute leukemias. Leukemia 1995; 9: 391-395.
7. Pui C-H, Ribeiro RC, Campana D, Raimondi SC, Hancock ML, Behm FG, Sandlund JT, Rivera GK, Evans WE, Crist WM, Krance R. Prognostic factors in the acute lymphoid and myeloid leukemias of infants. Leukemia 1996; 10: 952-956.
8. Taki T, Ida K, Bessho F, Hanada R, Kikuchi A, Yamamoto K, Sako M, Tsuchida M, Seto M, Ueda R, Hayashi Y. Frequency and clinical significance of the MLL gene rearrangements in infant acute leukemia. Leukemia 1996; 10: 1303-1307.
9. Hilden JM, Smith FO, Frestedt JL, McGlennen R, Howells WB, Sorensen PHB, Arthur DC, Woods WG, Buckley J, Bernstein ID, Kersey JH. MLL gene rearrangement, cytogenetic 11q23 abnormalities, and expression of the NG2 molecule in infant acute myeloid leukemia. Blood 1997; 89: 3801-3805.
10. Carroll A, Civin C, Schneider N, Dahl G, Pappo A, Bowman P, Emami A, Gross S, Alvarado C, Phillips C, Krischer J, Crist W, Head D, Gresik M, Ravindranath Y, Weinstein H. The t(1;22)(p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: a Pediatric Oncology Group study. Blood 1991; 78: 748-752.
11. Martinez-Climent JA. Molecular cytogenetics of childhood hematological malignancies. Leukemia 1997; 11: 1999-2021.
12. Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick HR, Sultan C. Proposed revised criteria for the classification of acute myeloid leukemia. A report of the French-American-British Cooperative Group. Ann Intern Med 1985; 103: 626-629.
13. Tsurusawa M, Katano N, Hirota T, Mimaya J, Horikoshi Y, Kawamura N, Yanai M, Kamitamari A, Tsuji Y, Fujimoto T. Treatment results in childhood acute myeloblastic leukemia - a report of clinical trials of a past decade from the Japanese Children's Cancer and Leukemia Study Group (CCLSG). Jpn J Clin Hematol 1997; 38: 505-512.
14. Bessho F, Kigasawa H, Tsuchida M, Tsukimoto I, Nakazawa S, Yamamoto M, Tsunematu Y, Yamada K, Sugita K, Ohkawa Y, Kaneko T, Kaku H, Inana I, Wada E, Kaneko M, Ito K, Shidara T. Improved prognosis of acute nonlymphocytic leukemia in children: results of the 12th ANLL protocol of Tokyo Children's Cancer Study Group. Acta Paediatr Jpn 1991; 33: 533-539.
15. Nagao T. Footprints of the Children's Leukemia Study Group of Japan. Jpn J Pediatr Hematol 1995; 9: 332-340.
16. Kobayashi H, Maseki N, Homma C, Sakurai M, Kaneko Y. Clinical significance of chromosome abnormalities in childhood acute lymphoblastic leukemia in Japan. Leukemia 1994; 8: 1944-1950.
17. ISCN 1995. An International System for Human Cytogenetic Nomenclature. Mitelman F (ed). Karger: Basel 1995.
18. Yamamoto K, Seto M, Komatsu H, Iida S, Akao Y, Kojima S, Kodera Y, Nakazawa S, Ariyoshi Y, Takahashi T, Ueda R. Two distinct portions of LTG19/ENL are involved in t(11;19) leukemia. Oncogene 1993; 8: 2617-2625.
19. Kobayashi H, Satake N, Maseki N, Sakashita A, Kaneko Y. The der(12)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia. Br J Haematol 1996; 94: 105-111.
20. Wlodarska I, La Starza R, Baens M, Dierlamm J, Uyttebroeck A, Selleslag D, Francine A, Mecucci C, Hagemeijer A, Van den Berghe H, Marynen P. Fluorescence in situ hybridization characterization of new translocations involving TEL(ETV6) in a wide spectrum of human of hematologic malignancies. Blood 1998; 91: 1399-1406.
21. Kaplan EL, Meier P. Nonparametric estimation for incomplete observations. J Am Stat Assoc 1958; 53: 457-481.
22. Peto R, Peto J. Asymptotically efficient rank invariant test procedures. J R Stat Soc (A) 1972; 135: 185-206.
23. Martinez-Climent JA, Thirman MJ, Espinosa III R, LeBeau MM, Rowley JD. Deletion of 11q23/MLL rearrangements in infants leukemia with fluorescence in situ hybridization and molecular analysis. Leukemia 1995; 9: 1299-1304.
24. Sorensen PHB, Chen CS, Smith FO, Arthur DC, Domer PH, Bernstein ID, Korsmeyer SJ, Hammond GD, Kersey JH. 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 1994; 93: 429-437.
25. Bower M, Parry P, Carter M, Lillington DM, Amess J, Lister TA, Evans G, Young BD. Prevalence and clinical correlations of MLL gene rearrangements in AML-M4/5. Blood 1994; 84: 3776-3780.
26. Moorman AV, Hagemeijer A, Charrin C, Rieder H, Sacker-Walker LM on behalf of the European 11q23 workshop participants. The translocations, t(11;19)(q23;p13.1) and t(11;19)(q23;p13.3): a cytogenetic and clinical profile of 53 patients. Leukemia 1998; 12: 805-810.
27. Kalwinsky D, Raimondi SC, Schell MJ, Mirro J Jr, Santana VM, Behm F, Dahl GV, Williams D. Prognostic importance of cytogenetic subgroups in de novo pediatric acute nonlymphocytic leukemia. J Clin Oncol 1990; 8: 75-83.
28. Martinez-Climent JA, Espinosa R III, Thirman MJ, LeBeau MM, Rowley JD. Abnormalities of chromosome band 11q23 and the MLL gene in pediatric myelomonocytic and monoblastic leukemias. Identification of the t(9;11) as an indicator of long survival. J Pediatr Hematol Oncol 1995; 17: 277-283.
29. Leblanc T, Auvrignon A, Michel G, Ansoborlo S, van den Akker J, Nelken B, Capodano A-M, Landman-Parker J, Baruchel A, Berger R, Schaison G, Leverger G. Prognostic value of cytogenetics in 250 children with acute myeloblastic leukemia treated in the LAME 89/91 protocol. Blood 1996; 88: (Suppl. 1): 634a.
30. Mrozek K, Heinonen K, Lawrence D, Carroll AJ, Koduru PRK, Rao KW, Strout MP, Hutchison RE, Moore JO, Mayer RJ, Schiffer CA, Bloomfield CD. Adult patients with de novo acute myeloid leukemia and t(9;11)(p22;q23) have a superior outcome to patients with other translocations involving band 11q23: a Cancer and Leukemia Group B study. Blood 1997; 90: 4532-4538.
31. Nakamura T, Alder H, Gu Y, Prasad R, Canaani O, Kamada N, Gale RP, Lange B, Crist WM, Nowell PC, Croce CM, Canaani E. Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs. Proc Natl Acad Sci USA 1993; 90: 4361-4365.
32. The Fourth International Workshop on Chromosomes in Leukemia: a prospective study of acute nonlymphocytic leukemia. Cancer Genet Cytogenet 1984; 11: 284-313.
33. Pui CH, Raimondi SC, Murphy SB, Ribeiro RC, Kalwinsky DK, Dahl GV, Crist WM, Williams DL. An analysis of leukemic cell chromosomal features in infants. Blood 1987; 69: 1289-1293.
34. Slater RM, Behrendt H, De Waal FC. Chromosome studies on acute nonlymphocytic leukemia in children. Pediatr Res 1983; 17: 398-405.