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Erschienen in: Annals of Hematology 10/2017

05.08.2017 | Original Article

Molecular analysis of more than 140 gene fusion variants and aberrant activation of EVI1 and TLX1 in hematological malignancies

verfasst von: Faramarz Ghasemian Sorbeni, Soheila Montazersaheb, Atefeh Ansarin, Ali Esfahani, Azim Rezamand, Ebrahim Sakhinia

Erschienen in: Annals of Hematology | Ausgabe 10/2017

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Abstract

Gene fusions are observed in abnormal chromosomal rearrangements such as translocations in hematopoietic malignancies, especially leukemia subtypes. Hence, it is critical to obtain correct information about these rearrangements in order to apply proper treatment techniques. To identify abnormal molecular changes in patients with leukemia, we developed a multiplex reverse transcriptase polymerase chain reaction (MRT-PCR) protocol and investigated more than 140 gene fusions resulting from variations of 29 prevalent chromosomal rearrangements along with EVI1 and TLX1 oncogenic expression in the presence of optimized primers. The potential of the MRT-PCR method was approved by evaluating the available cell lines as positive control and confirmed by sequencing. Samples from 53 patients afflicted with hematopoiesis malignancies were analyzed. Results revealed at least one chromosomal rearrangement in 69% of acute myeloid leukemia subjects, 64% of acute lymphoblastic leukemia subjects, and 81% of chronic myeloid leukemia subjects, as well as a subject with hypereosinophilic syndrome. Also, five novel fusion variants were detected. Results of this study also showed that chromosomal rearrangements, both alone and in conjunction with other rearrangements, are involved in leukemogenesis. Moreover, it was found that EVI1 is a suitable hallmark for hematopoietic malignancies.
Literatur
3.
Zurück zum Zitat Pallisgaard N, Hokland P, Riishoj DC, Pedersen B, Jorgensen P (1998) Multiplex reverse transcription-polymerase chain reaction for simultaneous screening of 29 translocations and chromosomal aberrations in acute leukemia. Blood 92(2):574–588PubMed Pallisgaard N, Hokland P, Riishoj DC, Pedersen B, Jorgensen P (1998) Multiplex reverse transcription-polymerase chain reaction for simultaneous screening of 29 translocations and chromosomal aberrations in acute leukemia. Blood 92(2):574–588PubMed
4.
Zurück zum Zitat Liu PP, Hajra A, Wijmenga C, Collins FS (1995) Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia. Blood 85(9):2289–2302PubMed Liu PP, Hajra A, Wijmenga C, Collins FS (1995) Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia. Blood 85(9):2289–2302PubMed
5.
Zurück zum Zitat Pandolfi PP, Alcalay M, Fagioli M, Zangrilli D, Mencarelli A, Diverio D, Biondi A, Lo Coco F, Rambaldi A, Grignani F et al (1992) Genomic variability and alternative splicing generate multiple PML/RAR alpha transcripts that encode aberrant PML proteins and PML/RAR alpha isoforms in acute promyelocytic leukaemia. EMBO J 11(4):1397–1407PubMedPubMedCentral Pandolfi PP, Alcalay M, Fagioli M, Zangrilli D, Mencarelli A, Diverio D, Biondi A, Lo Coco F, Rambaldi A, Grignani F et al (1992) Genomic variability and alternative splicing generate multiple PML/RAR alpha transcripts that encode aberrant PML proteins and PML/RAR alpha isoforms in acute promyelocytic leukaemia. EMBO J 11(4):1397–1407PubMedPubMedCentral
6.
Zurück zum Zitat Meyer-Monard S, Parlier V, Passweg J, Muhlematter D, Hess U, Bargetzi M, Kuhne T, Cabrol C, Gratwohl A, Jotterand M, Tichelli A (2006) Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia. Leukemia 20(2):247–253. doi:10.1038/sj.leu.2404044 PubMedCrossRef Meyer-Monard S, Parlier V, Passweg J, Muhlematter D, Hess U, Bargetzi M, Kuhne T, Cabrol C, Gratwohl A, Jotterand M, Tichelli A (2006) Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia. Leukemia 20(2):247–253. doi:10.​1038/​sj.​leu.​2404044 PubMedCrossRef
7.
Zurück zum Zitat Bonomi R, Giordano H, del Pilar MM, Bodega E, Landoni AI, Gallagher R, del Rosario UM (2000) Simultaneous PML/RARalpha and AML1/ETO expression with t(15;17) at onset and relapse with only t(8;21) in an acute promyelocytic leukemia patient. Cancer Genet Cytogenet 123(1):41–43PubMedCrossRef Bonomi R, Giordano H, del Pilar MM, Bodega E, Landoni AI, Gallagher R, del Rosario UM (2000) Simultaneous PML/RARalpha and AML1/ETO expression with t(15;17) at onset and relapse with only t(8;21) in an acute promyelocytic leukemia patient. Cancer Genet Cytogenet 123(1):41–43PubMedCrossRef
8.
Zurück zum Zitat Berger R, Bernheim A, Daniel MT, Flandrin G (1983) t(15;17) in a promyelocytic form of chronic myeloid leukemia blastic crisis. Cancer Genet Cytogenet 8(2):149–152PubMedCrossRef Berger R, Bernheim A, Daniel MT, Flandrin G (1983) t(15;17) in a promyelocytic form of chronic myeloid leukemia blastic crisis. Cancer Genet Cytogenet 8(2):149–152PubMedCrossRef
10.
Zurück zum Zitat Elia L, Mancini M, Moleti L, Meloni G, Buffolino S, Krampera M, De Rossi G, Foa R, Cimino G (2003) A multiplex reverse transcriptase-polymerase chain reaction strategy for the diagnostic molecular screening of chimeric genes: a clinical evaluation on 170 patients with acute lymphoblastic leukemia. Haematologica 88(3):275–279PubMed Elia L, Mancini M, Moleti L, Meloni G, Buffolino S, Krampera M, De Rossi G, Foa R, Cimino G (2003) A multiplex reverse transcriptase-polymerase chain reaction strategy for the diagnostic molecular screening of chimeric genes: a clinical evaluation on 170 patients with acute lymphoblastic leukemia. Haematologica 88(3):275–279PubMed
11.
Zurück zum Zitat Geng Z, Zhang H, Wang D, Xiao Y, Wang N, Li C, Huang L, Zhou J (2012) Combination of cytogenetic analysis and molecular screening in patients with de novo acute myeloid leukemia. J Huazhong Univ Sci Technolog Med Sci 32(4):501–510. doi:10.1007/s11596-012-0087-6 PubMedCrossRef Geng Z, Zhang H, Wang D, Xiao Y, Wang N, Li C, Huang L, Zhou J (2012) Combination of cytogenetic analysis and molecular screening in patients with de novo acute myeloid leukemia. J Huazhong Univ Sci Technolog Med Sci 32(4):501–510. doi:10.​1007/​s11596-012-0087-6 PubMedCrossRef
12.
Zurück zum Zitat Pruett SB, Obiri N, Kiel JL (1989) Involvement and relative importance of at least two distinct mechanisms in the effects of 2-mercaptoethanol on murine lymphocytes in culture. J Cell Physiol 141(1):40–45. doi:10.1002/jcp.1041410107 PubMedCrossRef Pruett SB, Obiri N, Kiel JL (1989) Involvement and relative importance of at least two distinct mechanisms in the effects of 2-mercaptoethanol on murine lymphocytes in culture. J Cell Physiol 141(1):40–45. doi:10.​1002/​jcp.​1041410107 PubMedCrossRef
14.
Zurück zum Zitat Sato T, Goyama S, Kataoka K, Nasu R, Tsuruta-Kishino T, Kagoya Y, Nukina A, Kumagai K, Kubota N, Nakagawa M, Arai S, Yoshimi A, Honda H, Kadowaki T, Kurokawa M (2014) Evi1 defines leukemia-initiating capacity and tyrosine kinase inhibitor resistance in chronic myeloid leukemia. Oncogene 33(42):5028–5038. doi:10.1038/onc.2014.108 PubMedPubMedCentralCrossRef Sato T, Goyama S, Kataoka K, Nasu R, Tsuruta-Kishino T, Kagoya Y, Nukina A, Kumagai K, Kubota N, Nakagawa M, Arai S, Yoshimi A, Honda H, Kadowaki T, Kurokawa M (2014) Evi1 defines leukemia-initiating capacity and tyrosine kinase inhibitor resistance in chronic myeloid leukemia. Oncogene 33(42):5028–5038. doi:10.​1038/​onc.​2014.​108 PubMedPubMedCentralCrossRef
15.
Zurück zum Zitat Raza A, Buonamici S, Lisak L, Tahir S, Li D, Imran M, Chaudary NI, Pervaiz H, Gallegos JA, Alvi MI, Mumtaz M, Gezer S, Venugopal P, Reddy P, Galili N, Candoni A, Singer J, Nucifora G (2004) Arsenic trioxide and thalidomide combination produces multi-lineage hematological responses in myelodysplastic syndromes patients, particularly in those with high pre-therapy EVI1 expression. Leuk Res 28(8):791–803. doi:10.1016/j.leukres.2003.11.018 PubMedCrossRef Raza A, Buonamici S, Lisak L, Tahir S, Li D, Imran M, Chaudary NI, Pervaiz H, Gallegos JA, Alvi MI, Mumtaz M, Gezer S, Venugopal P, Reddy P, Galili N, Candoni A, Singer J, Nucifora G (2004) Arsenic trioxide and thalidomide combination produces multi-lineage hematological responses in myelodysplastic syndromes patients, particularly in those with high pre-therapy EVI1 expression. Leuk Res 28(8):791–803. doi:10.​1016/​j.​leukres.​2003.​11.​018 PubMedCrossRef
16.
Zurück zum Zitat Smol T, Nibourel O, Marceau-Renaut A, Celli-Lebras K, Berthon C, Quesnel B, Boissel N, Terre C, Thomas X, Castaigne S, Dombret H, Preudhomme C, Renneville A (2015) Quantification of EVI1 transcript levels in acute myeloid leukemia by RT-qPCR analysis: a study by the ALFA Group. Leuk Res 39(12):1443–1447. doi:10.1016/j.leukres.2015.09.021 PubMedCrossRef Smol T, Nibourel O, Marceau-Renaut A, Celli-Lebras K, Berthon C, Quesnel B, Boissel N, Terre C, Thomas X, Castaigne S, Dombret H, Preudhomme C, Renneville A (2015) Quantification of EVI1 transcript levels in acute myeloid leukemia by RT-qPCR analysis: a study by the ALFA Group. Leuk Res 39(12):1443–1447. doi:10.​1016/​j.​leukres.​2015.​09.​021 PubMedCrossRef
17.
Zurück zum Zitat Stevens A, Hanson D, de Leonibus C, Whatmore A, Donn R, White DJ, Liu J, van den Heuvel-Eibrink MM, Saha V, Clayton PE, Meyer S (2014) EVI1 expression in childhood acute lymphoblastic leukaemia is not restricted to MLL and BCR/ABL rearrangements and is influenced by age. Blood Cancer J 4:e179. doi:10.1038/bcj.2013.76 PubMedPubMedCentralCrossRef Stevens A, Hanson D, de Leonibus C, Whatmore A, Donn R, White DJ, Liu J, van den Heuvel-Eibrink MM, Saha V, Clayton PE, Meyer S (2014) EVI1 expression in childhood acute lymphoblastic leukaemia is not restricted to MLL and BCR/ABL rearrangements and is influenced by age. Blood Cancer J 4:e179. doi:10.​1038/​bcj.​2013.​76 PubMedPubMedCentralCrossRef
18.
Zurück zum Zitat Kennedy MA, Gonzalez-Sarmiento R, Kees UR, Lampert F, Dear N, Boehm T, Rabbitts TH (1991) HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24. Proc Natl Acad Sci U S A 88(20):8900–8904PubMedPubMedCentralCrossRef Kennedy MA, Gonzalez-Sarmiento R, Kees UR, Lampert F, Dear N, Boehm T, Rabbitts TH (1991) HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24. Proc Natl Acad Sci U S A 88(20):8900–8904PubMedPubMedCentralCrossRef
19.
Zurück zum Zitat Aplan PD, Lombardi DP, Ginsberg AM, Cossman J, Bertness VL, Kirsch IR (1990) Disruption of the human SCL locus by “illegitimate” V-(D)-J recombinase activity. Science 250(4986):1426–1429PubMedCrossRef Aplan PD, Lombardi DP, Ginsberg AM, Cossman J, Bertness VL, Kirsch IR (1990) Disruption of the human SCL locus by “illegitimate” V-(D)-J recombinase activity. Science 250(4986):1426–1429PubMedCrossRef
20.
Zurück zum Zitat 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 trisomy 11. Cancer Res 56(6):1418–1425PubMed 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 trisomy 11. Cancer Res 56(6):1418–1425PubMed
21.
Zurück zum Zitat 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 M5. Blood 87(6):2496–2505PubMed 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 M5. Blood 87(6):2496–2505PubMed
22.
Zurück zum Zitat van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Muhlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH (1999) Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered. Oncogene 18(2):543–550. doi:10.1038/sj.onc.1202321 PubMedCrossRef van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Muhlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH (1999) Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered. Oncogene 18(2):543–550. doi:10.​1038/​sj.​onc.​1202321 PubMedCrossRef
24.
Zurück zum Zitat Rowe D, Strain L, Lowe C, Jones G (2007) A case of acute myeloid leukemia with inv(16)(p13q22) reveals a novel MYH11 breakpoint and a new CBF beta-MYH11 transcript variant. Haematologica 92(10):1433–1434. doi:10.3324/haematol.11536 PubMedCrossRef Rowe D, Strain L, Lowe C, Jones G (2007) A case of acute myeloid leukemia with inv(16)(p13q22) reveals a novel MYH11 breakpoint and a new CBF beta-MYH11 transcript variant. Haematologica 92(10):1433–1434. doi:10.​3324/​haematol.​11536 PubMedCrossRef
25.
Zurück zum Zitat Borkhardt A, Repp R, Haas OA, Leis T, Harbott J, Kreuder J, Hammermann J, Henn T, Lampert F (1997) Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23). Oncogene 14(2):195–202. doi:10.1038/sj.onc.1200814 PubMedCrossRef Borkhardt A, Repp R, Haas OA, Leis T, Harbott J, Kreuder J, Hammermann J, Henn T, Lampert F (1997) Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23). Oncogene 14(2):195–202. doi:10.​1038/​sj.​onc.​1200814 PubMedCrossRef
26.
Zurück zum Zitat Tse W, Zhu W, Chen HS, Cohen A (1995) A novel gene, AF1q, fused to MLL in t(1;11) (q21;q23), is specifically expressed in leukemic and immature hematopoietic cells. Blood 85(3):650–656PubMed Tse W, Zhu W, Chen HS, Cohen A (1995) A novel gene, AF1q, fused to MLL in t(1;11) (q21;q23), is specifically expressed in leukemic and immature hematopoietic cells. Blood 85(3):650–656PubMed
27.
Zurück zum Zitat Busson-Le Coniat M, Salomon-Nguyen F, Hillion J, Bernard OA, Berger R (1999) MLL-AF1q fusion resulting from t(1;11) in acute leukemia. Leukemia 13(2):302–306PubMedCrossRef Busson-Le Coniat M, Salomon-Nguyen F, Hillion J, Bernard OA, Berger R (1999) MLL-AF1q fusion resulting from t(1;11) in acute leukemia. Leukemia 13(2):302–306PubMedCrossRef
28.
Zurück zum Zitat Lee SG, Park TS, Yang JJ, Oh SH, Cho EH, Lee S, Oh D, Huh JY, Marschalek R, Meyer C (2012) Molecular identification of a new splicing variant of the MLL - MLLT11 fusion transcript in an adult with acute myeloid leukemia and t(1;11)(q21;q23). Acta Haematol 128(3):131–138. doi:10.1159/000338258 PubMedCrossRef Lee SG, Park TS, Yang JJ, Oh SH, Cho EH, Lee S, Oh D, Huh JY, Marschalek R, Meyer C (2012) Molecular identification of a new splicing variant of the MLL - MLLT11 fusion transcript in an adult with acute myeloid leukemia and t(1;11)(q21;q23). Acta Haematol 128(3):131–138. doi:10.​1159/​000338258 PubMedCrossRef
29.
Zurück zum Zitat Sagawa M, Shimizu T, Shimizu T, Awaya N, Mitsuhashi T, Ikeda Y, Okamoto S, Kizaki M (2006) Establishment of a new human acute monocytic leukemia cell line TZ-1 with t(1;11)(p32;q23) and fusion gene MLL-EPS15. Leukemia 20(9):1566–1571. doi:10.1038/sj.leu.2404305 PubMedCrossRef Sagawa M, Shimizu T, Shimizu T, Awaya N, Mitsuhashi T, Ikeda Y, Okamoto S, Kizaki M (2006) Establishment of a new human acute monocytic leukemia cell line TZ-1 with t(1;11)(p32;q23) and fusion gene MLL-EPS15. Leukemia 20(9):1566–1571. doi:10.​1038/​sj.​leu.​2404305 PubMedCrossRef
30.
Zurück zum Zitat Bernard OA, Mauchauffe M, Mecucci C, Van den Berghe H, Berger R (1994) A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL. Oncogene 9(4):1039–1045PubMed Bernard OA, Mauchauffe M, Mecucci C, Van den Berghe H, Berger R (1994) A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL. Oncogene 9(4):1039–1045PubMed
31.
Zurück zum Zitat Nourse J, Mellentin JD, Galili N, Wilkinson J, Stanbridge E, Smith SD, Cleary ML (1990) Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell 60(4):535–545PubMedCrossRef Nourse J, Mellentin JD, Galili N, Wilkinson J, Stanbridge E, Smith SD, Cleary ML (1990) Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell 60(4):535–545PubMedCrossRef
32.
Zurück zum Zitat Izraeli S, Kovar H, Gadner H, Lion T (1992) Unexpected heterogeneity in E2A/PBX1 fusion messenger RNA detected by the polymerase chain reaction in pediatric patients with acute lymphoblastic leukemia. Blood 80(6):1413–1417PubMed Izraeli S, Kovar H, Gadner H, Lion T (1992) Unexpected heterogeneity in E2A/PBX1 fusion messenger RNA detected by the polymerase chain reaction in pediatric patients with acute lymphoblastic leukemia. Blood 80(6):1413–1417PubMed
33.
Zurück zum Zitat Morris SW, Kirstein MN, Valentine MB, Dittmer KG, Shapiro DN, Saltman DL, Look AT (1994) Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma. Science 263(5151):1281–1284PubMedCrossRef Morris SW, Kirstein MN, Valentine MB, Dittmer KG, Shapiro DN, Saltman DL, Look AT (1994) Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma. Science 263(5151):1281–1284PubMedCrossRef
34.
Zurück zum Zitat Trumper L, Daus H, Merz H, von Bonin F, Loftin U, Cochlovius C, Moller P, Feller AC, Pfreundschuh M (1997) NPM/ALK fusion mRNA expression in Hodgkin and Reed-Sternberg cells is rare but does occur: results from single-cell cDNA analysis. Ann Oncol 8(Suppl 2):83–87PubMedCrossRef Trumper L, Daus H, Merz H, von Bonin F, Loftin U, Cochlovius C, Moller P, Feller AC, Pfreundschuh M (1997) NPM/ALK fusion mRNA expression in Hodgkin and Reed-Sternberg cells is rare but does occur: results from single-cell cDNA analysis. Ann Oncol 8(Suppl 2):83–87PubMedCrossRef
35.
Zurück zum Zitat Weisenburger DD, Gordon BG, Vose JM, Bast MA, Chan WC, Greiner TC, Anderson JR, Sanger WG (1996) Occurrence of the t(2;5)(p23;q35) in non-Hodgkin's lymphoma. Blood 87(9):3860–3868PubMed Weisenburger DD, Gordon BG, Vose JM, Bast MA, Chan WC, Greiner TC, Anderson JR, Sanger WG (1996) Occurrence of the t(2;5)(p23;q35) in non-Hodgkin's lymphoma. Blood 87(9):3860–3868PubMed
36.
Zurück zum Zitat Yoneda-Kato N, Look AT, Kirstein MN, Valentine MB, Raimondi SC, Cohen KJ, Carroll AJ, Morris SW (1996) The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1. Oncogene 12(2):265–275PubMed Yoneda-Kato N, Look AT, Kirstein MN, Valentine MB, Raimondi SC, Cohen KJ, Carroll AJ, Morris SW (1996) The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1. Oncogene 12(2):265–275PubMed
37.
Zurück zum Zitat Mitani K, Ogawa S, Tanaka T, Miyoshi H, Kurokawa M, Mano H, Yazaki Y, Ohki M, Hirai H (1994) Generation of the AML1-EVI-1 fusion gene in the t(3;21)(q26;q22) causes blastic crisis in chronic myelocytic leukemia. EMBO J 13(3):504–510PubMedPubMedCentral Mitani K, Ogawa S, Tanaka T, Miyoshi H, Kurokawa M, Mano H, Yazaki Y, Ohki M, Hirai H (1994) Generation of the AML1-EVI-1 fusion gene in the t(3;21)(q26;q22) causes blastic crisis in chronic myelocytic leukemia. EMBO J 13(3):504–510PubMedPubMedCentral
38.
Zurück zum Zitat Nucifora G, Begy CR, Kobayashi H, Roulston D, Claxton D, Pedersen-Bjergaard J, Parganas E, Ihle JN, Rowley JD (1994) Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations. Proc Natl Acad Sci U S A 91(9):4004–4008PubMedPubMedCentralCrossRef Nucifora G, Begy CR, Kobayashi H, Roulston D, Claxton D, Pedersen-Bjergaard J, Parganas E, Ihle JN, Rowley JD (1994) Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations. Proc Natl Acad Sci U S A 91(9):4004–4008PubMedPubMedCentralCrossRef
39.
Zurück zum Zitat Yamamoto K, Seto M, Iida S, Komatsu H, Kamada N, Kojima S, Kodera Y, Nakazawa S, Saito H, Takahashi T et al (1994) A reverse transcriptase-polymerase chain reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities. Blood 83(10):2912–2921PubMed Yamamoto K, Seto M, Iida S, Komatsu H, Kamada N, Kojima S, Kodera Y, Nakazawa S, Saito H, Takahashi T et al (1994) A reverse transcriptase-polymerase chain reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities. Blood 83(10):2912–2921PubMed
40.
Zurück zum Zitat Downing JR, Head DR, Raimondi SC, Carroll AJ, Curcio-Brint AM, Motroni TA, Hulshof MG, Pullen DJ, Domer PH (1994) The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia. Blood 83(2):330–335PubMed Downing JR, Head DR, Raimondi SC, Carroll AJ, Curcio-Brint AM, Motroni TA, Hulshof MG, Pullen DJ, Domer PH (1994) The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia. Blood 83(2):330–335PubMed
41.
Zurück zum Zitat Ivanov IC, Jitaru D, Grigore GE, Zlei M, Ivanov AV, Dumitras S, Carasevici E, Miron IC (2013) Infant acute leukemia with lineage switch at relapse expressing a novel t(4;11)(q21;q23) MLL-AF4 fusion transcript. Revista Româd de Medicin de Laborator 21:47–58. doi:10.2478/rrlm-2013-0017 Ivanov IC, Jitaru D, Grigore GE, Zlei M, Ivanov AV, Dumitras S, Carasevici E, Miron IC (2013) Infant acute leukemia with lineage switch at relapse expressing a novel t(4;11)(q21;q23) MLL-AF4 fusion transcript. Revista Româd de Medicin de Laborator 21:47–58. doi:10.​2478/​rrlm-2013-0017
42.
Zurück zum Zitat Corral J, Forster A, Thompson S, Lampert F, Kaneko Y, Slater R, Kroes WG, van der Schoot CE, Ludwig WD, Karpas A et al (1993) Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation. Proc Natl Acad Sci U S A 90(18):8538–8542PubMedPubMedCentralCrossRef Corral J, Forster A, Thompson S, Lampert F, Kaneko Y, Slater R, Kroes WG, van der Schoot CE, Ludwig WD, Karpas A et al (1993) Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation. Proc Natl Acad Sci U S A 90(18):8538–8542PubMedPubMedCentralCrossRef
44.
Zurück zum Zitat Curtis CE, Grand FH, Waghorn K, Sahoo TP, George J, Cross NC (2007) A novel ETV6-PDGFRB fusion transcript missed by standard screening in a patient with an imatinib responsive chronic myeloproliferative disease. Leukemia 21(8):1839–1841. doi:10.1038/sj.leu.2404728 PubMedCrossRef Curtis CE, Grand FH, Waghorn K, Sahoo TP, George J, Cross NC (2007) A novel ETV6-PDGFRB fusion transcript missed by standard screening in a patient with an imatinib responsive chronic myeloproliferative disease. Leukemia 21(8):1839–1841. doi:10.​1038/​sj.​leu.​2404728 PubMedCrossRef
45.
Zurück zum Zitat Golub TR, Barker GF, Lovett M, Gilliland DG (1994) Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77(2):307–316PubMedCrossRef Golub TR, Barker GF, Lovett M, Gilliland DG (1994) Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77(2):307–316PubMedCrossRef
46.
Zurück zum Zitat Redner RL, Rush EA, Faas S, Rudert WA, Corey SJ (1996) The t(5;17) variant of acute promyelocytic leukemia expresses a nucleophosmin-retinoic acid receptor fusion. Blood 87(3):882–886PubMed Redner RL, Rush EA, Faas S, Rudert WA, Corey SJ (1996) The t(5;17) variant of acute promyelocytic leukemia expresses a nucleophosmin-retinoic acid receptor fusion. Blood 87(3):882–886PubMed
47.
Zurück zum Zitat Hamaguchi H, Nagata K, Yamamoto K, Fujikawa I, Kobayashi M, Eguchi M (1998) Establishment of a novel human myeloid leukaemia cell line (FKH-1) with t(6;9)(p23;q34) and the expression of dek-can chimaeric transcript. Br J Haematol 102(5):1249–1256PubMedCrossRef Hamaguchi H, Nagata K, Yamamoto K, Fujikawa I, Kobayashi M, Eguchi M (1998) Establishment of a novel human myeloid leukaemia cell line (FKH-1) with t(6;9)(p23;q34) and the expression of dek-can chimaeric transcript. Br J Haematol 102(5):1249–1256PubMedCrossRef
48.
Zurück zum Zitat Chen S, Xue Y, Zhang X, Wu Y, Pan J, Wang Y, Ceng J (2005) A new human acute monocytic leukemia cell line SHI-1 with t(6;11)(q27;q23), p53 gene alterations and high tumorigenicity in nude mice. Haematologica 90(6):766–775PubMed Chen S, Xue Y, Zhang X, Wu Y, Pan J, Wang Y, Ceng J (2005) A new human acute monocytic leukemia cell line SHI-1 with t(6;11)(q27;q23), p53 gene alterations and high tumorigenicity in nude mice. Haematologica 90(6):766–775PubMed
49.
Zurück zum Zitat Kakuda H, Sato T, Hayashi Y, Enomoto Y, Takayama J, Ohira M, Seto M, Ueda R, Fuse A, Niimi H (1996) A novel human leukaemic cell line, CTS, has a t(6;11) chromosomal translocation and characteristics of pluripotent stem cells. Br J Haematol 95(2):306–318PubMedCrossRef Kakuda H, Sato T, Hayashi Y, Enomoto Y, Takayama J, Ohira M, Seto M, Ueda R, Fuse A, Niimi H (1996) A novel human leukaemic cell line, CTS, has a t(6;11) chromosomal translocation and characteristics of pluripotent stem cells. Br J Haematol 95(2):306–318PubMedCrossRef
50.
Zurück zum Zitat Miyoshi H, Kozu T, Shimizu K, Enomoto K, Maseki N, Kaneko Y, Kamada N, Ohki M (1993) The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript. EMBO J 12(7):2715–2721PubMedPubMedCentral Miyoshi H, Kozu T, Shimizu K, Enomoto K, Maseki N, Kaneko Y, Kamada N, Ohki M (1993) The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript. EMBO J 12(7):2715–2721PubMedPubMedCentral
51.
Zurück zum Zitat Matozaki S, Nakagawa T, Kawaguchi R, Aozaki R, Tsutsumi M, Murayama T, Koizumi T, Nishimura R, Isobe T, Chihara K (1995) Establishment of a myeloid leukaemic cell line (SKNO-1) from a patient with t(8;21) who acquired monosomy 17 during disease progression. Br J Haematol 89(4):805–811PubMedCrossRef Matozaki S, Nakagawa T, Kawaguchi R, Aozaki R, Tsutsumi M, Murayama T, Koizumi T, Nishimura R, Isobe T, Chihara K (1995) Establishment of a myeloid leukaemic cell line (SKNO-1) from a patient with t(8;21) who acquired monosomy 17 during disease progression. Br J Haematol 89(4):805–811PubMedCrossRef
53.
Zurück zum Zitat Van Vlierberghe P, van Grotel M, Tchinda J, Lee C, Beverloo HB, van der Spek PJ, Stubbs A, Cools J, Nagata K, Fornerod M, Buijs-Gladdines J, Horstmann M, van Wering ER, Soulier J, Pieters R, Meijerink JP (2008) The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia. Blood 111(9):4668–4680. doi:10.1182/blood-2007-09-111872 PubMedPubMedCentralCrossRef Van Vlierberghe P, van Grotel M, Tchinda J, Lee C, Beverloo HB, van der Spek PJ, Stubbs A, Cools J, Nagata K, Fornerod M, Buijs-Gladdines J, Horstmann M, van Wering ER, Soulier J, Pieters R, Meijerink JP (2008) The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia. Blood 111(9):4668–4680. doi:10.​1182/​blood-2007-09-111872 PubMedPubMedCentralCrossRef
54.
Zurück zum Zitat Rosati R, La Starza R, Barba G, Gorello P, Pierini V, Matteucci C, Roti G, Crescenzi B, Aloisi T, Aversa F, Martelli MF, Mecucci C (2007) Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. Haematologica 92(2):232–235PubMedCrossRef Rosati R, La Starza R, Barba G, Gorello P, Pierini V, Matteucci C, Roti G, Crescenzi B, Aloisi T, Aversa F, Martelli MF, Mecucci C (2007) Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. Haematologica 92(2):232–235PubMedCrossRef
55.
Zurück zum Zitat Pession A, Martino V, Tonelli R, Beltramini C, Locatelli F, Biserni G, Franzoni M, Freccero F, Montemurro L, Pattacini L, Paolucci G (2003) MLL-AF9 oncogene expression affects cell growth but not terminal differentiation and is downregulated during monocyte-macrophage maturation in AML-M5 THP-1 cells. Oncogene 22(54):8671–8676. doi:10.1038/sj.onc.1207125 PubMedCrossRef Pession A, Martino V, Tonelli R, Beltramini C, Locatelli F, Biserni G, Franzoni M, Freccero F, Montemurro L, Pattacini L, Paolucci G (2003) MLL-AF9 oncogene expression affects cell growth but not terminal differentiation and is downregulated during monocyte-macrophage maturation in AML-M5 THP-1 cells. Oncogene 22(54):8671–8676. doi:10.​1038/​sj.​onc.​1207125 PubMedCrossRef
57.
58.
Zurück zum Zitat Nakamura T, Alder H, Gu Y, Prasad R, Canaani O, Kamada N, Gale RP, Lange B, Crist WM, Nowell PC et al (1993) 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 U S A 90(10):4631–4635PubMedPubMedCentralCrossRef Nakamura T, Alder H, Gu Y, Prasad R, Canaani O, Kamada N, Gale RP, Lange B, Crist WM, Nowell PC et al (1993) 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 U S A 90(10):4631–4635PubMedPubMedCentralCrossRef
59.
Zurück zum Zitat Mitterbauer G, Zimmer C, Fonatsch C, Haas O, Thalhammer-Scherrer R, Schwarzinger I, Kalhs P, Jaeger U, Lechner K, Mannhalter C (1999) Monitoring of minimal residual leukemia in patients with MLL-AF9 positive acute myeloid leukemia by RT-PCR. Leukemia 13(10):1519–1524PubMedCrossRef Mitterbauer G, Zimmer C, Fonatsch C, Haas O, Thalhammer-Scherrer R, Schwarzinger I, Kalhs P, Jaeger U, Lechner K, Mannhalter C (1999) Monitoring of minimal residual leukemia in patients with MLL-AF9 positive acute myeloid leukemia by RT-PCR. Leukemia 13(10):1519–1524PubMedCrossRef
60.
61.
Zurück zum Zitat Park J, Kim M, Lim J, Kim Y, Han K, Kim JS, Lee S, Kim HJ, Min WS (2013) Variant of ETV6/ABL1 gene is associated with leukemia phenotype. Acta Haematol 129(2):78–82. doi:10.1159/000342490 PubMedCrossRef Park J, Kim M, Lim J, Kim Y, Han K, Kim JS, Lee S, Kim HJ, Min WS (2013) Variant of ETV6/ABL1 gene is associated with leukemia phenotype. Acta Haematol 129(2):78–82. doi:10.​1159/​000342490 PubMedCrossRef
62.
63.
Zurück zum Zitat Yamamoto K, Yakushijin K, Nakamachi Y, Miyata Y, Sanada Y, Tanaka Y, Okamura A, Kawano S, Hayashi Y, Matsuoka H, Minami H (2014) Extramedullary T-lymphoid blast crisis of an ETV6/ABL1-positive myeloproliferative neoplasm with t(9;12)(q34;p13) and t(7;14)(p13;q11.2). Ann Hematol 93(8):1435–1438. doi:10.1007/s00277-013-1975-y PubMedCrossRef Yamamoto K, Yakushijin K, Nakamachi Y, Miyata Y, Sanada Y, Tanaka Y, Okamura A, Kawano S, Hayashi Y, Matsuoka H, Minami H (2014) Extramedullary T-lymphoid blast crisis of an ETV6/ABL1-positive myeloproliferative neoplasm with t(9;12)(q34;p13) and t(7;14)(p13;q11.2). Ann Hematol 93(8):1435–1438. doi:10.​1007/​s00277-013-1975-y PubMedCrossRef
64.
Zurück zum Zitat Matsuo Y, Drexler HG, Takeuchi M, Orita K (1999) A novel biphenotypic B-cell precursor leukemia cell line (NALM-29) carrying t(9;22)(q34;q11) established from a patient with acute leukemia. Leuk Res 23(8):731–740PubMedCrossRef Matsuo Y, Drexler HG, Takeuchi M, Orita K (1999) A novel biphenotypic B-cell precursor leukemia cell line (NALM-29) carrying t(9;22)(q34;q11) established from a patient with acute leukemia. Leuk Res 23(8):731–740PubMedCrossRef
65.
Zurück zum Zitat Hermans A, Heisterkamp N, von Linden M, van Baal S, Meijer D, van der Plas D, Wiedemann LM, Groffen J, Bootsma D, Grosveld G (1987) Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia. Cell 51(1):33–40PubMedCrossRef Hermans A, Heisterkamp N, von Linden M, van Baal S, Meijer D, van der Plas D, Wiedemann LM, Groffen J, Bootsma D, Grosveld G (1987) Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia. Cell 51(1):33–40PubMedCrossRef
66.
Zurück zum Zitat Chaplin T, Bernard O, Beverloo HB, Saha V, Hagemeijer A, Berger R, Young BD (1995) The t(10;11) translocation in acute myeloid leukemia (M5) consistently fuses the leucine zipper motif of AF10 onto the HRX gene. Blood 86(6):2073–2076PubMed Chaplin T, Bernard O, Beverloo HB, Saha V, Hagemeijer A, Berger R, Young BD (1995) The t(10;11) translocation in acute myeloid leukemia (M5) consistently fuses the leucine zipper motif of AF10 onto the HRX gene. Blood 86(6):2073–2076PubMed
67.
Zurück zum Zitat Prasad R, Leshkowitz D, Gu Y, Alder H, Nakamura T, Saito H, Huebner K, Berger R, Croce CM, Canaani E (1994) Leucine-zipper dimerization motif encoded by the AF17 gene fused to ALL-1 (MLL) in acute leukemia. Proc Natl Acad Sci U S A 91(17):8107–8111PubMedPubMedCentralCrossRef Prasad R, Leshkowitz D, Gu Y, Alder H, Nakamura T, Saito H, Huebner K, Berger R, Croce CM, Canaani E (1994) Leucine-zipper dimerization motif encoded by the AF17 gene fused to ALL-1 (MLL) in acute leukemia. Proc Natl Acad Sci U S A 91(17):8107–8111PubMedPubMedCentralCrossRef
68.
Zurück zum Zitat Strehl S, Konig M, Meyer C, Schneider B, Harbott J, Jager U, von Bergh AR, Loncarevic IF, Jarosova M, Schmidt HH, Moore SD, Marschalek R, Haas OA (2006) Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants. Genes Chromosomes Cancer 45(11):1041–1049. doi:10.1002/gcc.20372 PubMedCrossRef Strehl S, Konig M, Meyer C, Schneider B, Harbott J, Jager U, von Bergh AR, Loncarevic IF, Jarosova M, Schmidt HH, Moore SD, Marschalek R, Haas OA (2006) Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants. Genes Chromosomes Cancer 45(11):1041–1049. doi:10.​1002/​gcc.​20372 PubMedCrossRef
69.
Zurück zum Zitat Licht JD, Chomienne C, Goy A, Chen A, Scott AA, Head DR, Michaux JL, Wu Y, DeBlasio A, Miller WH Jr et al (1995) Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17). Blood 85(4):1083–1094PubMed Licht JD, Chomienne C, Goy A, Chen A, Scott AA, Head DR, Michaux JL, Wu Y, DeBlasio A, Miller WH Jr et al (1995) Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17). Blood 85(4):1083–1094PubMed
70.
Zurück zum Zitat Mitani K, Kanda Y, Ogawa S, Tanaka T, Inazawa J, Yazaki Y, Hirai H (1995) Cloning of several species of MLL/MEN chimeric cDNAs in myeloid leukemia with t(11;19)(q23;p13.1) translocation. Blood 85(8):2017–2024PubMed Mitani K, Kanda Y, Ogawa S, Tanaka T, Inazawa J, Yazaki Y, Hirai H (1995) Cloning of several species of MLL/MEN chimeric cDNAs in myeloid leukemia with t(11;19)(q23;p13.1) translocation. Blood 85(8):2017–2024PubMed
71.
Zurück zum Zitat Kakihana K, Kubo F, Wakabayashi S, Kurosu T, Miki T, Murakami N, Miura O (2008) A novel variant form of MLL-ELL fusion transcript with t(11;19)(q23;p13.1) in chronic myelomonocytic leukemia transforming to acute myeloid leukemia. Cancer Genet Cytogenet 184(2):109–112. doi:10.1016/j.cancergencyto.2008.04.001 PubMedCrossRef Kakihana K, Kubo F, Wakabayashi S, Kurosu T, Miki T, Murakami N, Miura O (2008) A novel variant form of MLL-ELL fusion transcript with t(11;19)(q23;p13.1) in chronic myelomonocytic leukemia transforming to acute myeloid leukemia. Cancer Genet Cytogenet 184(2):109–112. doi:10.​1016/​j.​cancergencyto.​2008.​04.​001 PubMedCrossRef
72.
Zurück zum Zitat Uphoff CC, MacLeod RA, Denkmann SA, Golub TR, Borkhardt A, Janssen JW, Drexler HG (1997) Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines. Leukemia 11(3):441–447PubMedCrossRef Uphoff CC, MacLeod RA, Denkmann SA, Golub TR, Borkhardt A, Janssen JW, Drexler HG (1997) Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines. Leukemia 11(3):441–447PubMedCrossRef
73.
Zurück zum Zitat Romana SP, Mauchauffe M, Le Coniat M, Chumakov I, Le Paslier D, Berger R, Bernard OA (1995) The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood 85(12):3662–3670PubMed Romana SP, Mauchauffe M, Le Coniat M, Chumakov I, Le Paslier D, Berger R, Bernard OA (1995) The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood 85(12):3662–3670PubMed
74.
75.
Zurück zum Zitat Park TS, Kim JS, Song J, Lee KA, Yoon S, Suh B, Lee JH, Lee HJ, Kim JK, Choi JR (2009) Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis. Cancer Genet Cytogenet 188(2):103–107. doi:10.1016/j.cancergencyto.2008.09.002 PubMedCrossRef Park TS, Kim JS, Song J, Lee KA, Yoon S, Suh B, Lee JH, Lee HJ, Kim JK, Choi JR (2009) Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis. Cancer Genet Cytogenet 188(2):103–107. doi:10.​1016/​j.​cancergencyto.​2008.​09.​002 PubMedCrossRef
76.
77.
Zurück zum Zitat Hiorns LR, Min T, Swansbury GJ, Zelent A, Dyer MJ, Catovsky D (1994) Interstitial insertion of retinoic acid receptor-alpha gene in acute promyelocytic leukemia with normal chromosomes 15 and 17. Blood 83(10):2946–2951PubMed Hiorns LR, Min T, Swansbury GJ, Zelent A, Dyer MJ, Catovsky D (1994) Interstitial insertion of retinoic acid receptor-alpha gene in acute promyelocytic leukemia with normal chromosomes 15 and 17. Blood 83(10):2946–2951PubMed
78.
Zurück zum Zitat Vizmanos JL, Larrrayoz MJ, Odero MD, Lasa R, Gonzalez M, Novo FJ, Calasanz MJ (2002) Two new molecular PML-RARalpha variants: implications for the molecular diagnosis of APL. Haematologica 87(8):ELT37PubMed Vizmanos JL, Larrrayoz MJ, Odero MD, Lasa R, Gonzalez M, Novo FJ, Calasanz MJ (2002) Two new molecular PML-RARalpha variants: implications for the molecular diagnosis of APL. Haematologica 87(8):ELT37PubMed
79.
Zurück zum Zitat Zayed A, Couban S, Hayne O, Sparavalo N, Shawwa A, Sadek I, Greer W (2007) Acute promyelocytic leukemia: a novel PML/RARalpha fusion that generates a frameshift in the RARalpha transcript and ATRA resistance. Leuk Lymphoma 48(3):489–496. doi:10.1080/10428190601136163 PubMedCrossRef Zayed A, Couban S, Hayne O, Sparavalo N, Shawwa A, Sadek I, Greer W (2007) Acute promyelocytic leukemia: a novel PML/RARalpha fusion that generates a frameshift in the RARalpha transcript and ATRA resistance. Leuk Lymphoma 48(3):489–496. doi:10.​1080/​1042819060113616​3 PubMedCrossRef
80.
Zurück zum Zitat Oh SJ, Park TS, Lee JY, Mun YC, Seong CM, Marschalek R, Meyer C, Chung WS, Huh J (2013) Acute promyelocytic leukemia with a rare PML exon 4/ RARA exon 3 fusion transcript variant. Acta Haematol 130(3):176–180. doi:10.1159/000348551 PubMedCrossRef Oh SJ, Park TS, Lee JY, Mun YC, Seong CM, Marschalek R, Meyer C, Chung WS, Huh J (2013) Acute promyelocytic leukemia with a rare PML exon 4/ RARA exon 3 fusion transcript variant. Acta Haematol 130(3):176–180. doi:10.​1159/​000348551 PubMedCrossRef
81.
Zurück zum Zitat Jeziskova I, Razga F, Gazdova J, Doubek M, Jurcek T, Koristek Z, Mayer J, Dvorakova D (2010) A case of a novel PML/RARA short fusion transcript with truncated transcription variant 2 of the RARA gene. Mol Diagn Ther 14(2):113–117. doi:10.2165/11317400-000000000-00000 PubMedCrossRef Jeziskova I, Razga F, Gazdova J, Doubek M, Jurcek T, Koristek Z, Mayer J, Dvorakova D (2010) A case of a novel PML/RARA short fusion transcript with truncated transcription variant 2 of the RARA gene. Mol Diagn Ther 14(2):113–117. doi:10.​2165/​11317400-000000000-00000 PubMedCrossRef
82.
Zurück zum Zitat Kong XT, Ida K, Ichikawa H, Shimizu K, Ohki M, Maseki N, Kaneko Y, Sako M, Kobayashi Y, Tojou A, Miura I, Kakuda H, Funabiki T, Horibe K, Hamaguchi H, Akiyama Y, Bessho F, Yanagisawa M, Hayashi Y (1997) Consistent detection of TLS/FUS-ERG chimeric transcripts in acute myeloid leukemia with t(16;21)(p11;q22) and identification of a novel transcript. Blood 90(3):1192–1199PubMed Kong XT, Ida K, Ichikawa H, Shimizu K, Ohki M, Maseki N, Kaneko Y, Sako M, Kobayashi Y, Tojou A, Miura I, Kakuda H, Funabiki T, Horibe K, Hamaguchi H, Akiyama Y, Bessho F, Yanagisawa M, Hayashi Y (1997) Consistent detection of TLS/FUS-ERG chimeric transcripts in acute myeloid leukemia with t(16;21)(p11;q22) and identification of a novel transcript. Blood 90(3):1192–1199PubMed
84.
Zurück zum Zitat Ichikawa H, Shimizu K, Hayashi Y, Ohki M (1994) An RNA-binding protein gene, TLS/FUS, is fused to ERG in human myeloid leukemia with t(16;21) chromosomal translocation. Cancer Res 54(11):2865–2868PubMed Ichikawa H, Shimizu K, Hayashi Y, Ohki M (1994) An RNA-binding protein gene, TLS/FUS, is fused to ERG in human myeloid leukemia with t(16;21) chromosomal translocation. Cancer Res 54(11):2865–2868PubMed
85.
Zurück zum Zitat Jiang H, Qiu H, Xue Y, Pan J, Wu Y, Zhang J, Zheng J, Wang Q, Liang J, Chen S (2011) Establishment and characterization of a novel acute myeloid leukemia cell line, JIH-4, carrying a t(16;21)(p11.2;q22) and expressing the FUS-ERG fusion. Cancer Genet 204(4):219–223. doi:10.1016/j.cancergen.2011.02.005 PubMedCrossRef Jiang H, Qiu H, Xue Y, Pan J, Wu Y, Zhang J, Zheng J, Wang Q, Liang J, Chen S (2011) Establishment and characterization of a novel acute myeloid leukemia cell line, JIH-4, carrying a t(16;21)(p11.2;q22) and expressing the FUS-ERG fusion. Cancer Genet 204(4):219–223. doi:10.​1016/​j.​cancergen.​2011.​02.​005 PubMedCrossRef
86.
Zurück zum Zitat Takahashi H, Goto H, Eunabiki T, Fujii H, Yamazaki S, Fujioka K, Ikuta K, Kai S (2001) Expression of two types of E2A-HLF fusion proteins in YCUB-2, a novel cell line established from B-lineage leukemia with t(17;19). Leukemia 15(6):995–997PubMedCrossRef Takahashi H, Goto H, Eunabiki T, Fujii H, Yamazaki S, Fujioka K, Ikuta K, Kai S (2001) Expression of two types of E2A-HLF fusion proteins in YCUB-2, a novel cell line established from B-lineage leukemia with t(17;19). Leukemia 15(6):995–997PubMedCrossRef
87.
Zurück zum Zitat Hunger SP, Devaraj PE, Foroni L, Secker-Walker LM, Cleary ML (1994) Two types of genomic rearrangements create alternative E2A-HLF fusion proteins in t(17;19)-ALL. Blood 83(10):2970–2977PubMed Hunger SP, Devaraj PE, Foroni L, Secker-Walker LM, Cleary ML (1994) Two types of genomic rearrangements create alternative E2A-HLF fusion proteins in t(17;19)-ALL. Blood 83(10):2970–2977PubMed
89.
Zurück zum Zitat Pui C-H (2006) Childhood leukemias, 2nd edn. Cambridge University Press, CambridgeCrossRef Pui C-H (2006) Childhood leukemias, 2nd edn. Cambridge University Press, CambridgeCrossRef
90.
Zurück zum Zitat Steinleitner K, Rampetsreiter P, Koffel R, Ramanathan G, Mannhalter C, Strobl H, Wieser R (2012) EVI1 and MDS1/EVI1 expression during primary human hematopoietic progenitor cell differentiation into various myeloid lineages. Anticancer Res 32(11):4883–4889PubMedPubMedCentral Steinleitner K, Rampetsreiter P, Koffel R, Ramanathan G, Mannhalter C, Strobl H, Wieser R (2012) EVI1 and MDS1/EVI1 expression during primary human hematopoietic progenitor cell differentiation into various myeloid lineages. Anticancer Res 32(11):4883–4889PubMedPubMedCentral
91.
Zurück zum Zitat Kustikova OS, Schwarzer A, Stahlhut M, Brugman MH, Neumann T, Yang M, Li Z, Schambach A, Heinz N, Gerdes S, Roeder I, Ha TC, Steinemann D, Schlegelberger B, Baum C (2013) Activation of Evi1 inhibits cell cycle progression and differentiation of hematopoietic progenitor cells. Leukemia 27(5):1127–1138. doi:10.1038/leu.2012.355 PubMedCrossRef Kustikova OS, Schwarzer A, Stahlhut M, Brugman MH, Neumann T, Yang M, Li Z, Schambach A, Heinz N, Gerdes S, Roeder I, Ha TC, Steinemann D, Schlegelberger B, Baum C (2013) Activation of Evi1 inhibits cell cycle progression and differentiation of hematopoietic progenitor cells. Leukemia 27(5):1127–1138. doi:10.​1038/​leu.​2012.​355 PubMedCrossRef
92.
Zurück zum Zitat Barjesteh van Waalwijk van Doorn-Khosrovani S, Erpelinck C, van Putten WL, Valk PJ, van der Poel-van de Luytgaarde S, Hack R, Slater R, Smit EM, Beverloo HB, Verhoef G, Verdonck LF, Ossenkoppele GJ, Sonneveld P, de Greef GE, Lowenberg B, Delwel R (2003) High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients. Blood 101(3):837–845. doi:10.1182/blood-2002-05-1459 PubMedCrossRef Barjesteh van Waalwijk van Doorn-Khosrovani S, Erpelinck C, van Putten WL, Valk PJ, van der Poel-van de Luytgaarde S, Hack R, Slater R, Smit EM, Beverloo HB, Verhoef G, Verdonck LF, Ossenkoppele GJ, Sonneveld P, de Greef GE, Lowenberg B, Delwel R (2003) High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients. Blood 101(3):837–845. doi:10.​1182/​blood-2002-05-1459 PubMedCrossRef
93.
94.
Zurück zum Zitat Russell M, List A, Greenberg P, Woodward S, Glinsmann B, Parganas E, Ihle J, Taetle R (1994) Expression of EVI1 in myelodysplastic syndromes and other hematologic malignancies without 3q26 translocations. Blood 84(4):1243–1248PubMed Russell M, List A, Greenberg P, Woodward S, Glinsmann B, Parganas E, Ihle J, Taetle R (1994) Expression of EVI1 in myelodysplastic syndromes and other hematologic malignancies without 3q26 translocations. Blood 84(4):1243–1248PubMed
95.
Zurück zum Zitat Ferrando AA, Neuberg DS, Staunton J, Loh ML, Huard C, Raimondi SC, Behm FG, Pui CH, Downing JR, Gilliland DG, Lander ES, Golub TR, Look AT (2002) Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia. Cancer Cell 1(1):75–87PubMedCrossRef Ferrando AA, Neuberg DS, Staunton J, Loh ML, Huard C, Raimondi SC, Behm FG, Pui CH, Downing JR, Gilliland DG, Lander ES, Golub TR, Look AT (2002) Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia. Cancer Cell 1(1):75–87PubMedCrossRef
96.
Zurück zum Zitat Hatano M, Roberts CW, Minden M, Crist WM, Korsmeyer SJ (1991) Deregulation of a homeobox gene, HOX11, by the t(10;14) in T cell leukemia. Science 253(5015):79–82PubMedCrossRef Hatano M, Roberts CW, Minden M, Crist WM, Korsmeyer SJ (1991) Deregulation of a homeobox gene, HOX11, by the t(10;14) in T cell leukemia. Science 253(5015):79–82PubMedCrossRef
98.
Zurück zum Zitat Lichty BD, Ackland-Snow J, Noble L, Kamel-Reid S, Dube ID (1995) Dysregulation of HOX11 by chromosome translocations in T-cell acute lymphoblastic leukemia: a paradigm for homeobox gene involvement in human cancer. Leuk Lymphoma 16(3–4):209–215. doi:10.3109/10428199509049759 PubMedCrossRef Lichty BD, Ackland-Snow J, Noble L, Kamel-Reid S, Dube ID (1995) Dysregulation of HOX11 by chromosome translocations in T-cell acute lymphoblastic leukemia: a paradigm for homeobox gene involvement in human cancer. Leuk Lymphoma 16(3–4):209–215. doi:10.​3109/​1042819950904975​9 PubMedCrossRef
Metadaten
Titel
Molecular analysis of more than 140 gene fusion variants and aberrant activation of EVI1 and TLX1 in hematological malignancies
verfasst von
Faramarz Ghasemian Sorbeni
Soheila Montazersaheb
Atefeh Ansarin
Ali Esfahani
Azim Rezamand
Ebrahim Sakhinia
Publikationsdatum
05.08.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
Annals of Hematology / Ausgabe 10/2017
Print ISSN: 0939-5555
Elektronische ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-017-3075-x

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