A reverse transcriptase-polymerase chain reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities

Blood

Volumn 83, Issue 10, 1994, Pages 2912-2921

  Yamamoto, Kazuhito ^b   Seto, Masao ^a   Iida, Shinsuke ^b   Komatsu, Hirokazu ^b   Kamada, Nanao ^b   Kojima, Seiji ^b   Kodera, Yoshihisa ^b   Nakazawa, Shinpei ^b   Saito, Hidehiko ^b   Takahashi, Toshitada ^b   Ueda, Ryuzo ^b  

^a AICHI CANCER CENTER HOSPITAL   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA;

ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 11Q; CHROMOSOME 19; CHROMOSOME 4; CHROMOSOME 9; CHROMOSOME TRANSLOCATION 11; FEMALE; HUMAN; HUMAN TISSUE; INFANT; LABORATORY DIAGNOSIS; LEUKEMIA; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SECOND CANCER; SEQUENCE ANALYSIS; SOUTHERN BLOTTING;

EID: 0028325337     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v83.10.2912.2912     Document Type: Article

References (46)

1. Abe R, Sandberg AA: Significance of abnormalities involved chromosomal segment 11q22-25 in acute leukemia. Cancer Genet Cytogenet 13:121, 1984
2. Gibbons B, Katz FE, Ganly P, Chessells JM: Infant acute lymphoblastic leukemia with t(11; 19). Br J Haematol 74:264, 1990
3. Pui C-H, Frankel LS, Carroll AJ, Raimondi SC, Shuster JJ, Head DR, Crist WM, Land VJ, Pullen DJ, Steuber CP, Behm FG, Borowitz MJ: Clinical characteristics and treatment outcome of childhood acute lymphoblastic leukemia with the t(4; 11)(q21; q23): A collaborative study of 40 cases. Blood 77:440, 1991
4. Raimondi SC: Current status of cytogenetic research in childhood acute lymphoblastic leukemia. Blood 81:2237, 1993
5. Trent JM, Kaneko Y, Mitelman F: Report of the committee on structural chromosome changes in neoplasia. Cytogenet Cell Genet 51:533, 1989
6. Dewald GW, Morrison-DeLap SJ, Schuchard KA, Spurbeck JL, Pierre RV: A possible specific chromosome marker for monocytic leukemia: Three more patients with t(9; 11)(p22; q24) and another with t(11; 17)(q24; q21), each with acute monoblastic leukemia. Cancer Genet Cytogenet 8:203, 1983
7. Pui C-H, Behm FG, Raimondi SC, Dodge RK, George SL, Rivera GK, Mirro J Jr., Kalwinsky DK, Dahl GV, Murphy SB, Crist WM, Williams DL: Secondary acute myeloid leukemia in children treated for acute lymphoid leukemia. N Engl J Med 321:136, 1989
8. Prieto F, Palau F, Badia L, Beneyto M, Perez-Sirvent ML, Orts A, Castel V: 11q23 abnormalities in children with acute nonlymphocytic leukemia (M4-M5): Association with previous chemotherapy. Cancer Genet Cytogenet 45:1, 1990
9. Pui C-H, Ribeiro RC, Hancock ML, Rivera GK, Evans WE, Raimondi SC, Head DR, Behm FG, Mahmoud MH, Sandlund JT, Crist WM: Acute myeloid leukemia in children treated with epipodophyllotoxins for acute lymphoblastic leukemia. N Engl J Med 325:1682, 1991
10. Winick NJ, McKenna RW, Shuster JJ, Schneider NR, Borowitz MJ, Bowman WP, Jacaruso D, Kamen BA, Buchanan GR: Secondary acute myeloid leukemia in children with acute lymphoblastic leukemia treated with etoposide. J Clin Oncol 11:209, 1993
11. Sandoval C, Pui C-H, Bowman LC, Heaton D, Hurwitz CA, Raimondi SC, Behm FG, Head DR: Secondary acute myeloid leukemia in children previously treated with alkylating agents, intercalating topoisomerase II inhibitor, and irradiation. J Clin Oncol 11:1039, 1993
12. Hunger SP, Tkachuk DC, Amylon MD, Link MP, Carroll AJ, Welborn JL, Willman CL, Cleary ML: HRX involvement in de novo and secondary leukemias with diverse chromosome 11q23 abnormalities. Blood 81:3197, 1993
13. Ziemin-van der Poel S, McCabe NR, Gill HJ, Espinosa R III, Patel Y, Harden A, Rubinelli P, Smith SD, LeBeau MM, Rowly JD, Diaz MO: Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias. Proc Natl Acad Sci USA 88:10735, 1991
14. Yamamoto K, Seto M, Akao Y, Iida S, Nakazawa S, Oshimura M, Takahashi T, Ueda R: Gene rearrangement and truncated mRNA in cell lines with 11q23 translocation. Oncogene 8:479, 1993
15. Cimino G, Moir DT, Canaani O, Williams K, Crist WM, Katzav S, Cannizzaro L, Lange B, Nowell PC, Croce CM, Canaani E: Cloning of ALL-1, the locus involved in leukemias with the t(4; 11)(q21; q23), t(9; 11)(p22; q23), and t(11; 19)(q23; p13) chromosome translocations. Cancer Res 51:6712, 1991
16. Tkachuk DC, Kohler S, Cleary ML: Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 71:691, 1992
17. Djabali M, Selleri L, Parry P, Bower M, Young BD, Evans GA: A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukemias. Nature Genet 2:113, 1992
18. Gu Y, Nakamura T, Alder H, Prasad R, Canaani O, Cimino G, Croce CM, Canaani E: 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, 1992
19. 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 8:2617, 1993
20. Morgan GJ, Cotter F, Katz FE, Ridge SA, Domer P, Korsmeyer S, Wiedemann LM: Breakpoints at 11q23 in infant leukemias with the t(11; 19)(q23; p13) are clustered. Blood 80:2172, 1992
21. Gu Y, Cimino G, Alder H, Nakamura T, Prasad R, Canaani O, Moir DT, Jones C, Nowell PC, Croce CM, Canaani E: The (4; 11) (q21; q23) chromosome translocations in acute leukemias involve the VDJ recombinase. Proc Natl Acad Sci USA 89:10464, 1992
22. Iida S, Seto M, Yamamoto K, Komatsu H, Akao Y, Nakazawa S, Ariyoshi Y, Takahashi T, Ueda R: Molecular cloning of 19p13 breakpoint region in infantile leukemia with t(11; 19)(q23; p13) translocation. Jpn J Cancer Res 84:532, 1993
23. Morrissey J, Tkachuk DC, Milatovich A, Francke U, Link M, Cleary ML: A serine/proline-rich protein is fused to HRX in t(4; 11) acute leukemias. Blood 81:1124, 1993
24. Nakamura T, Alder H, Gu Y, Prasad R, Canaani O, Kamada N, Gale RP, Lange B, Crist WM, Nowell PC, Canaani E: Genes on chromosome 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs. Proc Natl Acad Sci USA 90:4631, 1993
25. Iida S, Seto M, Yamamoto K, Komatsu H, Tojo A, Asano S, Kamada N, Ariyoshi Y, Takahashi T, Ueda R: MLLT3 gene on 9p22 involved in t(9;11) leukemia encodes a serine/proline rich protein homologous to MLLT1 on 19p13. Oncogene 8:3085, 1993
26. Iida S, Saito M, Okazaki T, Seto M, Yamamoto K, Akao Y, Ogura M, Suzuki H, Ariyoshi Y, Koike K, Niita M, Takahashi T, Ueda R, Nakazawa S: Phenorypic and genotypic characterization of 14 leukemia and lymphoma cell lines with 11q23 translocations. Leuk Res 16:1155, 1992
27. Seto M, Jeager U, Hockett RD, Graninger W, Bennett S, Goldman P, Korsmeyer SJ: Alternative promoters and exons, somatic mutation and dereguration of Bcl-2-Ig fusion gene in lymphoma. EMBO J 7:123, 1988
28. Seto M, Yamamoto K, Iida S, Akao Y, Utsumi KR, Kubonishi I, Miyoshi I, Ohtsuki T, Yawata Y, Mamba M, Motokura T, Arnold A, Takahashi T, Ueda R: Gene rearrangement and overexpression of PRAD1 in Iymphoid malignancy with t(11;14)(q13;q32) translocation. Oncogene 7:1401, 1992
29. Corral J, Forster A, Thompson S, Lampert F, Kaneko Y, Slater R, Kroes WG, van der Schoot CE, Ludwig W-D, Karpas A, Pocock C, Cotter F, Rabbitts TH: Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation. Proc Natl Acad Sci USA 90:8538, 1993
30. Lee M-S, Chang K-S, Cabanillas F, Freireich EJ, Trujillo JM, Stass SA: Detection of minimal residual cells carrying the t(14; 18) by DNA sequence amplification. Science 237:175, 1987
31. Kawasaki ES, Clark SS, Coyne MY, Smith SD, Champlin R, Witte ON, McCormick FP: Diagnosis of chronic myeloid and acute lymphoblastic leukemias by detection of leukemia-specific mRNA sequences amplified in vitro. Proc Natl Acad Sci USA 85:5698, 1988
32. Miyamura K, Tanimoto M, Morishima Y, Horibe K, Yamamoto K, Akatsuka Y, Kodera Y, Kojima S, Matsuyama T, Hirabayashi N, Yazaki M, Imai K, Onozawa Y, Kanamaru A, Mizutani S, Saito H: Detection of Philadelphia chromosome-positive acute lymphoblastic leukemia by polymerase chain reaction: Possible eradication of minimal residual disease by marrow transplantation. Blood 79:1366, 1992
33. Hunger SP, Galili N, Carroll AJ, Crist WM, Link MP, Cleary ML: The t(1; 19)(q23; p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias. Blood 77:687, 1991
34. Privitera E, Kamps MM, Hayashi Y, Inaba T, Shapiro LH, Raimondi SC, Behm F, Hendershot L, Carroll AJ, Baltimore D, Look AT: Different molecular consequences of the 1; 19 chromosomal translocation in childhood B-cell precursor acute lymphoblastic leukemia. Blood 79:1781, 1992
35. Yokota S, Hansen-Hagge TE, Ludwig W-D, Reiter A, Raghavachar A, Kleihauer E, Bartram CR: Use of polymerase chain reactions to monitor minimal residual disease in acute lymphoblastic leukemia patients. Blood 77:331, 1991
36. Neale GAM, Menarguez J, Kitchingman GR, Fitzgerald TJ, Koehler M, Mirro J Jr, Goorha RM: Detection of minimal residual disease in T-cell acute lymphoblastic leukemia using polymerase chain reaction predicts impending relapse. Blood 78:739, 1991
37. Miller WH Jr., Kakizuka A, Frankel SR, Warrell RP Jr, De-Blasio A, Levine K, Evans RM, Dmitrovsky E: Reverse transcription polymerase chain reaction for the rearranged retinoic acid receptor α clarifies diagnosis and detects minimal residual disease in acute promyelocytic leukemia. Proc Natl Acad Sci USA 89:2694, 1992
38. Chang K-S, Lu J, Wang G, Trujillo JM, Estey E, Cork A, Chu D-T, Freireich EJ, Stass SA: The t(15; 17) breakpoint in acute promyelocytic leukemia cluster within two different sites of myl gene: Targets for the detection of minimal residual disease by polymerase chain reaction. Blood 79:554, 1992
39. Chen S-J, Chen Z, Chen A, Tong J-H, Dong S, Wang Z-Y, Waxman S, Zelent A: Occurrence of distant PML-RAR-α fuion gene isoforms in patients with acute promyelocytic leukemia detected by reverse transcriptase/polymerase chain reaction. Oncogene 7:1223, 1992
40. Castaigne S, Balitrand N, de Thé H, Dejean A, Degos L, Chomienne C: A PML/retinoic acid receptor α fusion transcript is constantly detected by RNA-based polymerase chain reaction in acute promyelocytic leukemia. Blood 79:3110, 1992
41. Biondi A, Rambaldi A, Pandolfi PP, Rossi V, Giudici G, Alcalay M, Coco FL, Diverio D, Pogliani EM, Lanzi EM, Mandelli F, Masera G, Barbui T, Pelicci PG: Molecular monitoring of the myl/retinoic acid receptor-α fusion gene in acute promyelocytic leukemia by polymerase chain reaction. Blood 80:492, 1992
42. Downing JR, Head DR, Curcio-Brint AM, Hulshof MG, Motroni TA, Raimondi SC, Carroll AJ, Drabkin HA, Willman C, Theil KS, Civin CI, Erickson P: An AML1/ETO fusion transcript is consistently detected by RNA-based polymerase chain reaction in acute myelogenous leukemia containing the (8; 21)(q22; q22) translocation. Blood 81:2860, 1993
43. Domer PH, Fakharzadeh SS, Chen C-S, Jockel J, Johansen L, Silverman GA, Kersey JH, Korsmeyer SJ: Acute mixed-lineage leukemia t(4; 11)(q21; q23) generates an MLL-AF4 fusion product. Proc Natl Acad Sci USA 90:7884, 1993
44. Kobayashi H, Espinosa R III, Thirman MJ, Fernald AA, Shannon K, Diaz MO, Le Beau MM, Rowley JD: Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization. Genes Chromosom Cancer 7:204, 1993
45. Chen C-S, Sorensen PHB, Domer PH, Reaman GH, Korsmeyer SJ, Heerema NA, Hammond D, Kersey JH: Molecular rearrangements on chromosome 11q23 predominate in infant acute lymphoblastic leukemia and are associated with specific biologic variables and poor outcome. Blood 81:2386, 1993
46. Mitani K, Sato Y, Kobayashi Y, Shibasaki Y, Kasuga M, Inaba T, Hayashi Y, Miura Y, Miyazono K, Hirai H, Urabe A, Takaku F: Heterogeneity in the breakpoints of chromosome 19 among acute leukemic patients with the t(11; 19)(q23; p13) translocation. Am J Hematol 31:253, 1989