80
Views
17
CrossRef citations to date
0
Altmetric
Original Article

Fish Analysis at Diagnosis in Acute Lymphoblastic Leukemia

Pages 441-449 | Accepted 01 Jul 1998, Published online: 01 Jul 2009

References

  • Rabbits T. H. Chromosomal translocations in human cancer. Nature 1994; 372: 143–149
  • Pui C. H., Crist W. M., Look A. T. Biology and clinical significance of cytogenetics abnormalities in childhood acute lymphoblastic leukemia. Blood 1990; 76: 1449–1463
  • Raimondi S. C. Current status of cytogenetic research in childhood acute lymphoblastic leukemia. Blood 1993; 82: 2237–2251
  • Copelan E. A., McGuire E. A. The biology and treatment of acute lymphoblastic leukemia in adults. Blood 1995; 85: 1151–1168
  • Pui C. H. Childhood leukemias. New Engl. J. Med. 1995; 332: 1618–1630
  • Crist W., Carroll A., Shuster J., Jackson J., Head D., Borowitz M., Behm F., Link M., Steuber P., Ragab A., Hirt A., Brock B., Land V., Pullen J. Philadelphia chromosome positive childhood acute lymphoblastic leukemia: Clinical and cytogenetic characteristics and treatment outcome. A Pediatric Oncology Group study. Blood 1990; 76: 489–495
  • Fletcher J. A., Lynch E. A., Kimball V. M., Donnelly M., Tantravahi R., Sallan S. E. Translocation (9;22) is associated with extremeiy poor prognosis in intensively treated children with acute lymphoblastic leukemia. Blood 1991; 77: 435–442
  • Groupe Francais de Cytogenetique Hematologique. Cytogenetic abnormalities in adult acute lymphoblastic leukemia: correlations with hematologic findings and outcome. A collaborative study of the Groupe Francais de Cytogenetique Hematologique. Blood 1996; 87: 3135–3142
  • Rieder H., Ludwig W. D., Gassman W., Maurer J., Janssen J. W. G., Gokbuget N., Schwartz S., Thiel E., Loffler H., Bartrani C. R., Hoelzer D., Fonatsch C. Prognostic significance of additional chromosome abnormalities in adult patients with Philadelphia chromosome positive acute lymphoblastic leukemia. Br. J. Haematol. 1996; 95: 678–691
  • Kantardjian H. M., Talpaz M., Dhingra K., Estey E., Keating M., Ku S., Trujillo J., Huh Y., Stass S., Kurzrock R. Significance of the P210 versus P190 molecular abnormalities in adults with Philadelphia chromosome‐positive acute leukemia. Blood 1991; 78: 2411–2417
  • Secker‐Walker L. M., Craig J. M., Hawkins J. M., Hoffbrand A. V. Philadelphia positive acute lymphoblastic lenkemia in adults: Age distribution, BCR breakpoint and prognostic significance. Leukemia 1991; 5: 196–202
  • Radich J. P., Kopecky K. J., Boldt D. H., Head D., Slovak M. L., Babu R., Kirk J., Lee A., Kessler P., Appelhaum F., Gehly G. Detection of BCR‐ABL fusion genes in adult acute lymphoblastic leukemia by the polymerase chain reaction. Leukemia 1994; 8: 1688–1694
  • Bentz M., Cahot G., Moos M., Speicher M. R., Gamer A., Lichter P., Dohner H. Detection of chimeric BCR‐ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization. Blood 1994; 83: 1922–1929
  • Seong D. C., Song M. Y., Henske E. P., Zimmerman S. O., Champlin R. E., Deisseroth A. B., Siciliano M. J. Analysis of interphase cells for the Philadelphia translocation using painting probe made by inter‐alu‐polymerase chain reaction from a radiation cell hybrid. Blood 1994; 83: 2268–2275
  • Sinclair P. B., Green A. R., Grace C., Nacheva E. P. Improved sensitivity of BCR‐ABL detection: A triple‐prohe three‐color fluorescence in situ hybridization system. Blood 1997; 90: 1395–1402
  • Cox M. C., Maffei M., Buffolino S., Del Poeta G., Venditti A., Cantonetti M., Aronica G., Aquilina P., Masi M., Ama‐dori S. a comparative analysis of FISH, RT‐PCR, and cytogenetics for the diagnosis of BCR‐ABL‐positive leuke‐mias. Am. J. Clin. Pathol. 1998; 109: 24–31
  • Dewald G. W., Wyatt W. A., Juneau A. L., Carlson R. O., Zinsmeister A. R., Jalal S. M., Spurheck J. L., Silver R. T. Highly sensitive fluorescence in situ hybridization method to detect double BCR‐ABL fusion and monitor response to therapy in chronic myeloid leukemia. Blood 1998; 91: 3357–3365
  • Pui C. H., Frankel L. S., Carroll A. J., Raimondi S. C., Shuster J. J., Head D. R., Crist W. M., Land V. J., Pullen D. J., Steuher C. P. Clinical characteristics and treatment outcome of childhood acute lymphoblastic leukemia with the t(4;11)(q21;q23): A collaborative study of 40 cases. Blood 1991; 77: 440–447
  • Cimino G., Lo Coco F., Biondi A., Elia L., Luciano A., Croce C. M., Masera G., Mandelli F., Canaani E. ALL‐1 gene at chromosome 11q23 is consistently altered in acute leukemia of early infancy. Blood 1993; 82: 544–546
  • Behm F. G., Raimondi S. C., Frestedt J. L., Liu Q., Crist W. M., Downing J. R., Rivera G. K., Kersey J. H., Pui C. H. Rearrangement of the MLL gene confers a poor prognosis in childhood acute lymphoblastic leukemia, regardless of presenting age. Blood 1996; 87: 2870–2877
  • Bernard O. A., Berger R. Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations. Genes, Chromos. Cancer 1995; 13: 75–85
  • Ruhnitz J. E., Behm F. G., Downing J. R. 11q23 rearrangements in acute leukemia. Leikemia 1996; 10: 7442
  • Tkachuk D. C., Kohler S., Cleary M. L. Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 1992; 71: 691–698
  • Djabali M., Selleri L., Parry P., Bower M., Young B. D., Evans G. A. A trithorax‐like gene is interrupted by chromosome 11q23 translocations in acute leukemias. Nat. Genet. 1992; 2: 113–118
  • Keamey L., Bower M., Gibbons B., Das S., Chaplin T., Nacheva E., Chessells J. M., Reeves B., Riley J. H., Lister T. A., Young B. D. Chromosome 11q23 translocations in both infant and adult acute leukemias are detected by in situ hybridization with a yeast artificial chromosome. Blood 1992; 80: 1659–1665
  • Kobayashi H., Espinosa R., Thirman M. J., Davis E. M., Diaz M. O., Le Beau M. M., Rowley J. D. Variability of 11q23 rearrangements in hematopoietic cell lines identified with fluorescence in situ hybridization. Blood 1993; 81: 3027–3033
  • Caligiuri M. A., Strout M. P., Schichman S. A., Mrozek K., Arthur D. C., Herzig G. P., Baer M. R., Schiffer C. A., Heino‐nen K., Knuutika S., Nousiainen T., Ruutu T., Block A. M. W., Schulman P., Peersen‐Bjergaard J., Croce C. M., Bloomfield C. D. Partial tandem duplication of ALLI as a recurrent molecular defect in acute myeloid leukemia with trisomy 11. Cancer Rex 1996; 56: 1418–1425
  • Romana S. P., Le Coniat M., Berger R. A new recurrent translocation in acute lymphoblastic leukemia. Genes Chromosomes Cuncer 1994; 9: 186–191
  • Romana S. P., Mauchauffe M., Le Coniat M., Churnakov I., Le Paslier D., Berger R., Bernard O. A. The t( 12, 21) of acute lymphoblastic leukemia results in a TEL‐AMLl gene fusion. Blood 1995; 85: 3662–3670
  • Kobayashi H., Satake N., Maseki N., SakdShitd A., Kaneko Y. the der(21)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
  • Raynaud S., Cave H., Baens M., Bastard C., Cacheux V., Grosgeorge J., Guidal‐Giroux C., Gno C., Vilmer E., Marynen P., Grandchamp B. The 12;21 trabslocation involving TEL and deletion of the other TEL allele: Two frequently associated alterations found in childhood acute lymphohlastic leukemia. Blood 1996; 87: 2891–2899
  • Borkhardt A., Cazzaniga G., Viehmann S., Vdlsecchi M. G., Ludwig W. D., Burci L., Mangioni S., Schrappe M., Riehm H., Lampert F., Basso G., Masera G., Harbott J., Biondi A. Incidence and clinical relevance of TEL/AMLl fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Bloud 1997; 90: 571–577
  • Rubnitz J. E., Downing J. R., Pui C. H., Shurtleff S. A., Raimondi S. C., Evans W. E., Head D. R., Crist W. M., Rivera G. K., Hancock M. L., Boyett J. M., Buijs A., Grosveld G., Behm F. G. TEL gene rearrangement in acute lymphoblastic leukemia: A new genetic marker with prognostic significance. J. Clin. Oncol. 1997; 15: 1150–1157
  • Harbott J., Viehmann S., Borkhardt A., Henze G., Lampert F. Incidence of TEL/AMLl fusion gene analyzed consecutively in children with acute lymphoblastic leukemia in relapse. Blood 1998; 90: 4933–4937
  • Seeger K., Adams H. P., Buchwald D., Beyermann B., Kre‐mens B., Niemeyer C., Ritter J., Schwabe D., Harms D., Schrappe M., Henze G. TEL‐AMLI fusion transcript in relapsed childhood acute lymphoblastic leukemia. Blood 1998; 91: 1716–1722
  • Secker‐Walker L. M., Prentice H. G., Durrant J., Richards S., Hall E., Harrison G. Cytogenetics adds independent prognostic information in adults with acute lymphoblastic leukaemia on MRC trial UKALL XA. Br. J. Haematol. 1997; 96: 601–610
  • Jackson J. F., Boyett J., Pullen J., Brock B., Patterson R., Land V., Borowitz M., Head D., Crist W. Favorable prognosis associated with hyperdiploidy in children with acute lymphoblastic leukemia correlates with extra chromosome 6. Cancer 1990; 66: 1183–1189
  • Harris M. B., Shuster J. J., Carroll A., Look A. T., Borowitz M. J., Crist W. M., Nitschke R., Pullen J., Steuber C. P., Land V. J. Trisomy of leukemic cell chromosomes 4 and 10 identifies children with B‐progenitor cell acute lym‐phoblastic leukemia with a very low risk of treatment failure: a Pediatric Oncology Group study. Blood 1992; 79: 3316–3324
  • Moorman A. V., Clark C., Farrell D. M., Hawkins J. M., Martineau M., Secker‐Walker L. M. Probes for hidden hyperdiploidy in acute lymphoblastic leukaemia. Genes Chromosomes Cancer 1996; 16: 40–45
  • Ritterbach J., Hiddemann W., Beck J. D., Schrappe M., Janka‐Schaub G., Ludwig W. D., Harbott J., Lampert F. Detection of hyperdiploid karyotypes (50 chromosomes) in childhood acute lymphohlastic leukemia (ALL) using fluorescence in situ hybridization (FISH). Leukemia 1998; 12: 427–433
  • Kahru R., Siitonen S., Tanner M., Keinanen M., Makiper‐naa A., Lehtinen M., Vilpo J. A., Isola J. Genetic aberrations in pediatric acute lymphoblastic leukemia by comparative genomic hybridization. Cancer Genet. Cyrogenet. 1997; 95: 123–129
  • Paszek‐Vigier M., Talmant P., Mechinaud F., Garand R., Harousseau J. L., Bataille R., Avet‐Loiseau H. Comparative genomic hybridization is a powerful tool, complementary to cytogenetics, to identify chromosomal abnormalities in childhood acute lymphoblastic leukaemia. Br. J. Haematol. 1997; 99: 589–596
  • Haas O. A., Henn T., Romanakis K., du Manoir S., Len‐gauer C. Comparative genomic hybridization as part of a new diagnostic strategy in childhood hyperdiploid acute lymphoblastic leukemia. Leukemia 1998; 12: 474–481

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.