84
Views
8
CrossRef citations to date
0
Altmetric
Original

Diagnostic Application of FISH to Hematological Malignancies

The Journal as a University—pathology

, Ph.D.
Pages 807-814 | Published online: 10 Aug 2003

References

  • Druker B.J., Talpaz M., Resta D.J., et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N. Engl. J. Med. 2001; 344: 1031–1037
  • An International System for Human Cytogenetic Nomenclature (1995). F. Mitelman. S. Karger, Basel 1995
  • Speicher M.R., Ballard S.G., Ward D.C. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat. Genet. 1996; 12: 368–375
  • Schrock E., du Manoir S., Veldman T., et al. Multicolor spectral karyotyping of human chromosomes. Science 1996; 273: 494–497
  • Rowley J.D. A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinicrine fluorescence and Giemsa staining. Nature 1973; 243: 290–293
  • Ben-Neriah Y., Daley G.Q., Mes-Masson A.-M., et al. The chronic myelogenous leukemia-specific P210 protein is the product of the bcr/abl hybrid gene. Science 1986; 233: 212–214
  • Faderal S., Talpaz M., Estrov Z., et al. The biology of chronic myeloid leukemia. N. Engl. J. Med. 1999; 341: 164–172
  • Tkachuk D.C., Westbrook C.A., Andreeff M., et al. Detection of BCR-ABL fusion in chronic myelogenous leukemia by in situ hybridization. Science 1990; 259: 559–562
  • Dewald G.W., Wyatt W.A., Juneau A.L., et al. 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
  • Sinclair P.B., Nacheva E.P., Leversha M., et al. Large deletions of the t(9;22) breakpoint are common and may identify a poor prognosis subgroup of patients with chronic myeloid leukemia. Blood 2000; 95: 738–744
  • Cohen N., Rozenfeld-Granot G., Hardan I., et al. Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis. Cancer Genet. Cytogenet. 2001; 128: 114–119
  • Mrozek K., Heinonen K., de la Chapelle A., et al. Clinical significance of cytogenetics in acute myeloid leukemia. Semin. Oncol. 1997; 24: 17–31
  • Nucifora G., Rowley J.D. AML1 and the 8;21 and 3;21 translocations in acute and chronic myeloid leukemia. Blood 1995; 86: 1–14
  • Wang Q., Stacey T., Binder M., et al. Disruption of Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis. Proc. Natl Acad. Sci. USA 1996; 93: 3444–3449
  • Grimwade D., Biondi A., Mozziconacci M.-J., et al. Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): result of the European Working Party. Blood 2000; 96: 1297–1308
  • He L.-Z., Guidez F., Triboli C., et al. Distinct interactions of PML-RARα and PLZF-RARα with co-repressors determine differential responses to RA in APL. Nat. Genet. 1998; 18: 126–135
  • Liu P.P., Castilla L.H., Adya N. The leukemogenic function of the inv(16) fusion gene CBFB-MYH11. Transcription Factors, K. Ravid, J.D. Licht. Wiley-Liss. 2001; 379–391
  • Haferlach T., Winkemann M., Loffler H., et al. The abnormal eosinophils are part of the leukemic cell population in acute myelomonocytic leukemia with abnormal eosinophils (AML M4Eo) and carry the pericentric inversion 16: a combination of May-Grunwald-Giemsa staining with fluorescence in situ hybridization. Blood 1996; 87: 2459–2463
  • Ziemen-van der Poel S., McCabe N.R., Gill H.J., et al. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias [published erratum appear in Proc. Natl Acad. Sci. USA 1992, 89, 4220]. Proc. Natl Acad. Sci. USA 1991; 88: 10735–10739
  • Rowley J.D. The role of chromosomal translocations in leukemogenesis. Semin. Hematol. 1999; 36: 59–72
  • Van den Berghe H., Michaux L. 5q−, twenty-five years later: a synopsis. Cancer Genet. Cytogenet. 1997; 94: 1–7
  • Horrigan S.K., Arbieva Z.H., Xie H.Y., et al. Delineation of minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31. Blood 2000; 95: 2372–2377
  • Najfeld, V.; Montella, L.; Scalise, A.; et al. Exploring polycythemia vera with FISH: additional cryptic 9p is the most frequent abnormality detected. Br. J. Haematol. 2002, 1–9.
  • Greenberg P., Cox C., Le Beau M.M., et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997; 89: 2079–2088
  • Rubinitz J.E., Pui C.H., Downing J.R. The role of TEL fusion genes in pediatric leukemia. Leukemia 1999; 13: 6–13
  • Appelbaum F.R. Molecular diagnosis and clinical decisions in adult acute leukemia. Semin. Hematol. 1999; 36: 401–410
  • Dohner H., Stilgenbauer S., Benner A., et al. Genomic aberrations and survival in chronic lymphocytic leukemia. N. Engl. J. Med. 2000; 343: 1910–1916
  • Liu Y., Hermanson M., Grander D., et al. 13q deletions in lymphoid malignancies. Blood 1995; 86: 1911–1915
  • Perez-Simon J.A., Garcia-Sanz R., Tabernaro M.D., et al. Prognostic value of numerical chromosome aberrations in multiple myeloma: a FISH analysis of 15 different chromosomes. Blood 1998; 91: 3366–3371
  • Desikan R., Barlogie B., Saweyer J., et al. Results of high-dose therapy for 1000 patients with multiple myeloma: durable complete remissions and superior survival in the absence of chromosome 13 abnormalities. Blood 2000; 95: 4008–4010
  • Stammatopoulos K., Kosmas C., Belessi C., et al. Molecular insights into the immunopathogenesis of follicular lymphoma. Blood 2000; 96: 808–822
  • Siebert R., Mathiesen P., Harder S., et al. Application of interphase fluorescence in situ hybridization for the detection of the Burkitt translocation t(8;14)(q24;q32) in B-cell lymphomas. Blood 1998; 91: 984–990
  • Ye H.B. BCL6 in the pathogenesis of non-Hodgkin's lymphoma. Cancer Investig. 2000; 18: 356–365
  • Siebert R., Matthisen P., Harder S., et al. Application of interphase cytogenetics for detection of t(11;14)(q13;q32) in mantle cell lymphoma. Ann. Oncol. 1998; 9: 519–526
  • Dierlamm J., Wlodarska I., Michauc L., et al. Genetic abnormalities in marginal zone B-cell lymphoma. Hematol. Oncol. 2000; 18: 1–13
  • Morris S.W., Kirstein M., Valentine M., et al. Fusion of a kinase gene ALK to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma. Science 1994; 263: 1281–1284
  • Benharroch D., Meguerin-Bedoyan Z., Lamant L., et al. ALK-positive lymphoma: a single disease with a broad spectrum of morphology. Blood 1998; 91: 2076–2084

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.