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The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia

Abstract

We applied multicolor spectral karyotyping (SKY) to a panel of 29 newly diagnosed pediatric pre B-cell ALLs with normal and abnormal G-banded karyotypes to identify cryptic translocations and define complex chromosomal rearrangements. By this method, it was possible to define all add chromosomes in six cases, a cryptic t(12;21)(p13;q11) translocation in six cases, marker chromosomes in two cases and refine the misidentified aberrations by G-banding in two cases. In addition, we identified five novel non-recurrent translocations – t(2;9)(p11.2;p13), t(2;22) (p11.2;q11.2), t(6;8)(p12;p11), t(12;14)(p13;q32) and t(X;8)(p22.3;q?). Of these translocations, t(2;9), t(2;22) and t(12;14) were identified by G-banding analysis and confirmed by SKY. We characterized a t(12;14)(p13;q32) translocation by FISH, and identified a fusion of TEL with IGH for the first time in ALL. We identified a rearrangement of PAX5 locus in a case with t(2;9)(p11.2;p13) by FISH and defined the breakpoint telomeric to PAX5 in der(9)t(3;9)(?;p13). These studies demonstrate the utility of using SKY in combination with G-banding and FISH to augment the precision with which chromosomal aberrations may be identified in tumor cells.

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References

  1. Greaves M . Molecular genetics, natural history and the demise of childhood leukemia Eur J Cancer 1999 35: 173–185

    Article  CAS  PubMed  Google Scholar 

  2. Sallan SE, Golub TR, Pui CH, Campana D, Evans WE, Behm FG, Billett A . Acute lymphoblastic leukemia. In: McArthur JR, Schechter GP, Platt OS, Bafus JL (eds) Hematology – Education Program American Society of Hematology: Washington DC 1997 103–119

    Google Scholar 

  3. Margolin JF, Poplack DG . Acute lymphoblastic leukemia. In: Pizzo PA, Poplack DG (eds) Principles and Practice of Pediatric Oncology, 3rd edn Lippincott-Raven: Philadelphia 1997 409–462

    Google Scholar 

  4. Romana SP, Le Coniat M, Berger R . t(12;21). A new recurrent translocation in acute lymphoblastic leukemia Genes Chromosomes Cancer 1994 9: 186–191

    Article  CAS  PubMed  Google Scholar 

  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 lymphoblastic leukemia Proc Natl Acad Sci USA 1995 92: 4917–4921

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Romana SP, Mauchauffe M, Le Coniat M, Chumakov I, Le Paslier D, Berger R, Bernard OA . The t(12;21) of acute lymphoblastic leukemia results in a Tel-AML1 gene fusion Blood 1995 85: 3662–3670

    CAS  PubMed  Google Scholar 

  7. Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenkensen D, Garini Y, Ried T . Muticolor spectral karyotyping of human chromosomes Science 1996 273: 494–497

    Article  PubMed  Google Scholar 

  8. Speicher MR, Ballard SG, Ward DC . Karyotyping human chromosomes by combinatorial multi-fluor FISH Nat Genet 1996 12: 368–375

    Article  CAS  PubMed  Google Scholar 

  9. Van Limbergen H, Poppe B, Michaux L, Herens C, Brown J, Noens L, Berneman Z, De Bock R, De Paepe A, Speleman F . Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using m-FISH Genes Chromosomes Cancer 2002 33: 66–72

    Article  Google Scholar 

  10. Brown J, Jawad M, Twigg SR, Saracoglu K, Sauerbrey A, Thomas AE, Elis R, Harbott, Kearney L . A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay Blood 2002 99: 2526–2531

    Article  CAS  PubMed  Google Scholar 

  11. Mitelman F (ed). ISCN (1995).An International System for Human Cytogenetic Nomenclature Karger: Basel 1995

  12. Rao PH, Cigudosa JC, Ning Y, Calasanz MJ, Iida S, Tagawa S, Michaeli J, Klein B, Dalla-Favera R, Jhanwar SC, Ried T, Chaganti RSK . Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma Blood 1998 92: 1743–1748

    CAS  PubMed  Google Scholar 

  13. Salomon-Nguyen F, Della-Valle V, Mauchauffe M, Busson-Le Coniat M, Ghysdael J, Berger R, Bernard O . The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion Proc Natl Acad Sci USA 2000 97: 6757–6762

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Cazzaniga G, Tosi S, Aloisi A, Giudici G, Daniotti M, Pioltelli P, Kearney L, Biondi A . The tyrosine kinase Abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): molecular cloning of both reciprocal transcripts Blood 1999 94: 4370–4373

    CAS  PubMed  Google Scholar 

  15. Peeters P, Wlodarska I, Baens M, Criel A, Selleslag D, Hagemeijer A, Van den Berghe H, Marynen P . Fusion of ETV6 to MDS/EVI1 as a result of t(3;12)(q26;p13) in myeloproliferative disorders Cancer Res 1997 57: 564–569

    CAS  PubMed  Google Scholar 

  16. Cools J, Bilhou-Nabera C, Wlodarska I, Cabrol C, Talmant P, Bernard P, Hagemeijer A, Marynen P . Fusion of a novel gene, BTL, to ETV6 in acute myeloid leukemias with a t(4;12)(q11-q12;p13) Blood 1999 94: 1820–1824

    CAS  PubMed  Google Scholar 

  17. Yagasaki F, Jinnai I, Yoshida S, Yokoyama Y, Matsuda A, Kusumoto S, Kobayashi H, Terasaki H, Ohyashiki K, Asou N, Murohashi I, Bessho M, Hirashima K . Fusion of TEL/ETV6 to a novel ACS2 in myelodysplastic syndrome and acute myelogenous leukemia with t(5;12)(q31;p13) Genes Chromosomes Cancer 1999 26: 192–202

    Article  CAS  PubMed  Google Scholar 

  18. Golub TR, Barker GF, Lovett M, Gilliland DG . Fusion of PDGF receptor to a novel ets-like, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation Cell 1994 77: 307–316

    Article  CAS  PubMed  Google Scholar 

  19. Suto Y, Sato Y, Smith SD, Rowley JD, Bohlander SK . A t(6;12)(q23;p13) results in the fusion of ETV6 to a novel gene, STL, in a B-cell ALL cell line Genes Chromosomes Cancer 1997 18: 254–268

    Article  CAS  PubMed  Google Scholar 

  20. Lacronique V, Boureux A, Valle VD, Poirel H, Quang CT, Mauchauffe M, Berthou C, Lessard M, Berger R, Ghysdael J, Bernard OA . A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia Science 1997 278: 1309–1312

    Article  CAS  PubMed  Google Scholar 

  21. 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 1995 55: 34–38

    CAS  PubMed  Google Scholar 

  22. Chase A, Reiter A, Burci L, Cazzaniga G, Biondi A, Pickard J, Roberts IAG, Goldman JM, Cross NCP . Fusion of ETV6 to the caudal-related homeobox gene CDX2 in acute myeloid leukemia with the t(12;13)(p13;q12) Blood 1999 93: 1025–1031

    CAS  PubMed  Google Scholar 

  23. Knezevich SR, McFadden DE, Tao W, Lim JF, Sorensen PHB . A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma Nat Genet 1998 18: 184–187

    Article  CAS  PubMed  Google Scholar 

  24. Buijs A, Sherr S, van Baal S, van Bezouw S, van der Plas D, Geurts van Kessel A, Riegman P, Lekanne 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 MN1 gene on 22q11 Oncogene 1995 10: 1511–1519

    CAS  PubMed  Google Scholar 

  25. Tosi S, Jochen H, Teigler-Schlegel, Haas OA, Pirc-Danoewwunta HP, Harrison CJ, Biondi A, Cazzaniga G, Kempski H, Scherer SW, Kearney L . t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia Genes Chromosomes Cancer 2000 29: 325–332

    Article  CAS  PubMed  Google Scholar 

  26. Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, Lynch SA, Lindsay S, Custard E, Belloni E, Wilson DI, Wadey R, Goodman F, Orstavik KH, Monclair T, Robson S, Reardon W, Burn J, Scambler P, Strachan T . A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis Nat Genet 1998 20: 358–361

    Article  CAS  PubMed  Google Scholar 

  27. Veldman T, Vignon C, Schrock E, Rowley JD, Ried T . Hidden chromosome abnormalities in hematological malignancies detected by multicolor spectral karyotyping Nat Genet 1997 15: 406–410

    Article  CAS  PubMed  Google Scholar 

  28. Rowley JD, Reshmi S, Carlson K, Roulston D . Spectral karyotype analysis of T-cell acute leukemia Blood 1999 93: 2038–2042

    CAS  PubMed  Google Scholar 

  29. Mohr B, Bornhauser M, Thiede C, Schakel U, Schaich M, Illmer T, Pascheberg U, Ehninger G . Comparison of spectral karyotyping and conventional cytogenetics in 39 patients with acute myeloid leukemia and myelodysplastic syndrome Leukemia 2000 14: 1031–1038

    Article  CAS  PubMed  Google Scholar 

  30. Kakazu N, Taniwaki M, Horiike S, Nishida K, Tatekawa T, Nagai M, Takayuki T, Akaogi T, Inazawa J, Ohki M, Abe T . Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome Genes Chromosomes Cancer 1999 26: 336–345

    Article  CAS  PubMed  Google Scholar 

  31. Zhang FF, Murata-Collins JL, Gaytan P, Forman SJ, Kopecky KJ, Willman CL, Appelbaum FR, Slovak ML . Twenty-Four-Color spectral karyotyping reveals chromosome aberrations in cytogenetically normal acute myeloid leukemia Genes Chromosomes Cancer 2000 28: 318–328

    Article  CAS  PubMed  Google Scholar 

  32. Pan Y, Kytola S, Farnebo F, Wang N, Liu WO, Nupponen N, Isola J, Visakorpi T, Bergerheim US, Larsson C . Characterization of chromosomal abnormalities in prostate cancer cell lines by spectral karyotyping Cytogenet Cell Genet 1999 87: 225–232

    Article  CAS  PubMed  Google Scholar 

  33. Kytola S, Rummukainen J, Nordgren A, Karhu R, Farnebo F, Isola J, Larsson C . Chromosomal alterations in 15 breast cancer cell lines by comparative genomic hybridization and spectral karyotyping Genes Chromosomes Cancer 2000 28: 308–317

    Article  CAS  PubMed  Google Scholar 

  34. Mathew S, Rao PH, Dalton J, Downing JR, Raimondi SC . Multicolor spectral karyotyping identifies novel translocations in childhood acute lymphoblastic leukemia Leukemia 2001 15: 468–472

    Article  CAS  PubMed  Google Scholar 

  35. Iida S, Rao PH, Nallasivam P, Hibshoosh H, Butler M, Louie D . C, Dyomin V, Ohno H, Chaganti R.S.K, Dalla-Favera R. The t(9;14)(p25;q32) chromosomal translocation associated with lymphoplasmacytoid lymphoma involves the PAX-5 gene Blood 1996 88: 4110–4117

    CAS  PubMed  Google Scholar 

  36. Czerny T, Schaffner G, Busslinger M . DNA sequence recognition by Pax proteins: bipartite structure of the paired domain and its binding site Genes Dev 1993 7: 2048–2061

    Article  CAS  PubMed  Google Scholar 

  37. Admas B, Dorfer P, Aguzzi A, Kozmik, Urabanek P, Maurer-fogy I, Busslinger M . Pax-5 encodes the translocation factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis Genes Dev 1992 6: 1589–1607

    Article  Google Scholar 

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Acknowledgements

This study was partially supported by a research grant from the Fleming-Davenport Foundation.

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Lu, X., Harris, C., Cooley, L. et al. The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia. Leukemia 16, 2222–2227 (2002). https://doi.org/10.1038/sj.leu.2402662

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