Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies

Blood

Volumn 91, Issue 4, 1998, Pages 1399-1406

  Wlodarska, Iwona ^b   La Starza, Roberta ^b   Baens, Mathijs ^b   Dierlamm, Judith ^b   Uyttebroeck, Ann ^b   Selleslag, Dominik ^b   Francine, Adrien ^b   Mecucci, Cristina ^b   Hagemeijer, Anne ^b   Van Den Berghe, Herman ^b   Marynen, Peter ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

HELIX LOOP HELIX PROTEIN;

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 12P; CHROMOSOME TRANSLOCATION; CHRONIC MYELOID LEUKEMIA; CLINICAL ARTICLE; CYTOGENETICS; DIMERIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE REARRANGEMENT; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; NONHODGKIN LYMPHOMA; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0032520176     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v91.4.1399     Document Type: Article

References (27)

1. Golub TR, Barker GF, Lovett M, Gilliland DG: Fusion of PDGF receptor b to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77:307, 1994
2. Peeters P, Wlodarska I, Baens M, Criel A, Selleslag D, Hagemeijer A, Van den Berghe H, Marynen P: Fusion of ETV6 to MDS/ETV1 as a result of t(3;12)(q26;p13) in myeloproliferative disorders.Cancer Res 57:564, 1997
3. Papadopoulos P, Ridge SA, Boucher CA, Stocking C, Wiedemann LM: The novel activation of ABL by fusion to an ets-related gene, TEL. Cancer Res 55:34, 1995
4. Romana SP, Mauchauffé M, Leconiat M, Chumakov I, Le Paslier D, Berger R, Bernard OA: The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion1 Blood 85:3662, 1995
5. Golub TR, Barker GF, Bohlander SK, Hiebert SW, Ward DC, Bray-Ward P, Morgan E, Raimondi SC, Rowley JD, Gilliland DG: Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute 1 lymphoblastic leukemia. Proc Natl Acad Sci USA 92:4917, 1995
6. Buijs A, Sherr S, van Baal S, van Bezouw S, van der Plas D, Geurts van Kessel A, Riegman P, Lekanne R, Deprez R, Zwarthoff E, Hagemeijer A, Grosveld G: Translocation (12;22)(p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MNI gene in 22q11.Oncogene 10:1511, 1995
7. Bohlander SK, Yohsimasa S, Sato T, Smith SD, Rowley JD: A t(6;12)(q23:p13) results in the fusion of ETV6 to a novel gene, STL, in a B-cell ALL cell line. Leukemia 10:2002, 1996
8. ISCN: Supplement to an International System for Human Cytogenetic Nomenclature, in Mitelman F (ed): Guidelines for Cancer Cytogenetics. Basel, Switzerland, Karger, 1995
9. Dierlamm J, Wlodarska I, Michaux L, La Starza R, Zeller W, Mecucci C, Van den Berghe H: Successful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. Genes Chromosom Cancer 16:216, 1996
10. Baens M, Peeters P, Guo C, Aerssens J, Marynen P: Genomic organisation of TEL: The human ETS variant gene 6 (ETV6). Genome Res 6:404, 1996
11. Green ED, Idol JR, Mohr-Tidwell RM, Braden VV, Peluso DC, Fulton RS, Massa HF, Magness CL, Wilson AM, Kimura J, Weissenbach J, Trask B: Integration of physical, genetic and cytogenetic maps of human chromosome 7: Isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. Hum Mol Genet 3:489, 1994
12. Keen TJ, Inglehearn CF, Green ED, Cunningham AF, Patel RJ, Peacock RE, Gerken S, White R, Weissenbach J, Bhattacharya SS: A YAC contig spanning the dominant Retinitis pigmentosa locus (RP9) on chromosome 7p. Genomics 28:383, 1995
13. Chumakov IM, Rigault P, Le Gall I, Bellanne-Chantelot C, Billafult A, Guillou S, Soularue P, Guasconi G, Poullier E, Gros I, Belova M, Sambucy J-L, Susini L, Gervy P, Gilbert F, Beaufils S, Bui H, Massart C, De Tand M-F, Dukasz F, Lecoulant S, Ougen P, Perrot V, Saumier M, Soravito C, Bahouayila R, Cohen-Akenine A, Barillot EM, Bertrand S, Codani J-J, Caterina D, Georges I, Lacroix B, Lucotte G, Sahbatou M, Schmit C, Sangouard M, Nguyen S, Muselet D, Vignal A, Morissette J, Menninger J, Lieman J, Desai T, Banks A, Bray-Ward P, Ward D, Hudson T, Gerety S, Foote S, Stein L, Page DC, Lander ES, Weissenbach J, Le Paslier D, Cohen D: A YAC contig map of the human genome. Nature 377:175, 1995
14. Morris SW, Foust JT, Valentine MB, Roberts WM, Shapiro DN, Look AT: Sublocalization of the chromosome 5 breakpoint of the 3;5 translocation in myelodysplastic syndromes and acute myeloid leukemia. Genes Chromosom Cancer 5:385-391, 1992
15. Taniwaki M, Matsuda F, Jauch A, Nishida K, Takashima T, Tagawa S, Sugiyama H, Misawa S, Abe T, Kashima K: Detection of 14q32 translocations in B-cell malignancies by in situ hybridization with yeast artificial chromosome clones containing the human IgH gene locus. Blood 83:2962, 1994
16. Wlodarska I, Mecucci C, Marynen P, Quo C, Franckx D, La Starza R, Aventin A, Bosly MF, Martelli JJ, Cassiman JJ, Van den Berghe H: TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) or its variant t(10;12)(q24;p13). Blood 85:2848, 1995
17. Billson AL, Latham M, Jalihal S, Martin K, Walker DA: Balanced 7;12 translocation associated with minimally differentiated acute myeloid leukemia. Cancer Genet Cytogenet 73:171, 1994
18. Cuneo A, Ferrant A, Michaux JL, Boogaerts M, Demuynck H, Van Orshoven A, Criel A, Stul M. Dal Cin P, Hernandez J, Chatelain B, Doyen C, Louwagie A, Castoldi G, Cassiman JJ, Van den Berghe H: Cytogenetic profile of minimally differentiated (FAB MO) acute myeloid leukemia: Correlation with clinicobiologic findings. Blood 85:3688, 1995
19. FujimuraT, Ohyashiki K, Ohyashiki JH, Kawakubo K, Iwabuchi A, Kodama A, Toyama K: Two additional cases of acute myeloid leukemia with t(7;11)(p15;p15) having low neutrophil alkaline phosphatase scores. Cancer Genet Cytogenet 68:143, 1993
20. Mecucci C, Van Orshoven A, Boogaerts M, Michaux JL, Van den Berghe H: Characterization of deletions of chromosome 7 short arm occurring as primary karyotypic anomaly in acute myeloid leukemia. Br J Haematol 71:13, 1989
21. Keene P, Mendelow B, Pinto MR, Bezwoda W, MacDougall L, Falkson G, Ruff P, Bernstein R: Abnormalities of chromosome 12p13 and malignant proliferation of eosinophils: A nonrandom association. Br J Haematol67:25, 1987
22. Uckun FM, Gajl-Peczalska KJ, Provisor AJ, Heerema NA: Immunophenotype-karyotype associations in human acute lymphoblastic leukemia. Blood 73:271, 1989
23. Raimondi SC, Privitera E, Williams DL, Look AT, Behm F, Rivera GK, Crist WM, Pui C-H: New recurring chromosomal translocations in childhood acute lymphoblastic leukemia. Blood 77:2016, 1991
24. Romana SP, Poirel H, Leconiat M, Flexor M-A, Mauchauffé M, Jonveaux P, Macintyre EA, Berger R, Bernard OA: High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood 86:4263, 1995
25. Raynaud S, Cavé H, Baens M, Bastard C, Cacheux V, Grosgeorge J, Guidal-Giroux C, Guo C, Vilmer E, Marynen P, Grandchamp B: The 12;21 translocation involving TEL and deletion of the other TEL allele: Two frequently associated alterations found in childhood acute lymphoblastic leukemia. Blood 87:2891, 1996
26. Wlodarska I, Baens M, Peeters P, Aerssens J, Mecucci C, Brock P, Marynen P, Van den Berghe H: Biallelic alterations of both ETV6 and CDKN1B genes in a t( 12;21 ) childhood ALL case Cancer Res 56:2655, 1996
27. Golub TR, Goga A, Barker G, Afar DEH, McLaughlin J, Bohlander SK, Rowley JD, Witte ON, Gilliland AG: Oligomerization of the ABL tyrosine kinase by the Ets protein TEL in Human leukemia. Mol Cell Biol 16:4107, 1996