Acute Leukemia with Structural Rearrangements of Chromosome 3

References

• Rowley J.D., Potter D. Chromosomal banding patterns in acute nonlymphocytic leukemia. Blood 1976; 47: 705–721
   PubMed Web of Science ®Google Scholar
• Golomb H.M., Vardiman J., Rowley J.D. Acute nonlymphocytic leukemia in adults: Correlations with Q-banded chromosomes. Blood 1976; 48: 9–21
   PubMed Web of Science ®Google Scholar
• Sweet D.L., Golomb H.M., Rowley J.D., Vardiman J.M. Acute myelogenous leukemia and thrombocythemia associated with an abnormality of chromosome No. 3. Cancer Genetics and Cytogenetics 1979; 1: 33–37
   Web of Science ®Google Scholar
• Bernstein R., Pinto M.R., Behr A., Mendelow B. Chromosome 3 abnormalities in acute nonlymphocytic leukemia (ANLL) with abnormal thrombopoiesis: Report of three patients with a “new” inversion anomaly and a further case of homologous translocation. Blood 1982; 60: 613–617
   PubMed Web of Science ®Google Scholar
• Norrby A., Ridell B., Swolin B., Westin J. Rearrangement of chromosome No. 3 in a case of preleukemia with thrombocytosis. Cancer Genetics and Cytogenetics 1982; 5: 257–263
   PubMed Web of Science ®Google Scholar
• Bitter M.A., Neilly M.E., LeBeau M.M., Pearson M.G., Rowley J.D. Rearrangements of chromosome 3 involving bands 3q21 and 3q26 are associated with normal or elevated platelet counts in acute nonlymphocytic leukemia. Blood 1985; 66: 1362–1370
   PubMed Web of Science ®Google Scholar
• Carbonell F., Hoelzer D., Thiel E., Bartl R. Ph1-positive CML associated with megakaryocyte hyperplasia and thrombocythemia and an abnormality of chromosome no. 3. Cancer Genetics and Cytogenetics 1982; 6: 153–161
   PubMed Web of Science ®Google Scholar
• Bargolie B., Hittelman W., Spitzer G., Trujillo J.M., Hart J.S., Smallwood L., Drewinko B. Correlation of DNA distribution abnormalities with cytogenetic findings in human adult leukemia and lymphoma. Cancer Res. 1977; 37: 4400–4407
   PubMed Web of Science ®Google Scholar
• Bernstein R., Bagg A., Pinto M., Lewis D., Mendelow B. Chromosome 3q21 abnormalities associated with hyperactive thrombopoiesis in acute blastic transformation of chronic myeloid leukemia. Blood 1986; 68: 652–657
   PubMed Web of Science ®Google Scholar
• Shimazaki C., Fujita N., Nakanishi S., Nishio A., Haruyama H., Nakagawa M., Ijichi H., Nishida K., Misawa S. Inversion of chromosome 3 in a case of chronic myelogenous leukemia with abnormal thrombopoiesis. Cancer Genetics and Cytogenetics 1986; 20: 121–127
   PubMed Web of Science ®Google Scholar
• Mecucci C., Vermaelen K., Tricot G., Louwagie A., Michaux J.L., Bosly A., Thomas J., Barbieri D., Van Den Berghe H. 3q-, 3q+ anomaly in malignant proliferations in humans. Cancer Genetics and Cytogenetics 1983; 9: 367–381
   Web of Science ®Google Scholar
• Pintado T., Ferro M.T., San Roman C., Mayayo M., Larana J.G. Clinical correlations of the 3q21;q26 cytogenetic anomaly. A leukemic or myelodysplastic syndrome with preserved or increased platelet production and lack of response to cytotoxic drug therapy. Cancer 1985; 55: 535–541
   PubMed Web of Science ®Google Scholar
• Jenkins R.B., Tefferi A., Solberg L.A., Jr., Dewald G.W. Acute leukemia with abnormal thrombopoiesis and inversions of chromosome 3. Cancer Genetics and Cytogenetics 1989; 39: 167–179
   PubMed Web of Science ®Google Scholar
• Lee E.J., Schiffer C.A., Tomiyasu T., Testa J.R. Clinical and cytogenetic correlations of abnormal megakaryocy-topoiesis in patients with acute leukemia and chronic myelogenous leukemia in blast crisis. Leukemia 1990; 4: 350–353
   PubMed Web of Science ®Google Scholar
• Walter T.A., Morgan R., Ondreyco S., Sandberg A.A. Apparent duplication of inv(3) (q21q26) in one of five cases with inv(3) in myelodysplastic syndromes and acute leukemia. Am. J. Hematol 1990; 33: 210–214
   PubMed Web of Science ®Google Scholar
• Ohyashiki K., Ohyashiki J.H., Hojo H., Ohtaka M., Toyama K., Sugita K., Nakazawa S., Sugiura K., Nakazawa K., Nagasawa T., Enomoto Y., Watanabe Y. Cytogenetic findings in adult acute leukemia and myeloproliferative disorders with an involvement of megakaryocyte lineage. Cancer 1990; 65: 940–948
   PubMed Web of Science ®Google Scholar
• Pedersen B. Thrombopoiesis and structural rearrangements of the long arm of chromosome 3. Review and analysis of data on 64 published patients. Leukemia and Lymphoma 1990; 1: 93–102
   Google Scholar
• Grigg A.P., Gascoyne R.D., Phillips G.L., Horsman D.E. Clinical, haematological and cytogenetic features in 24 patients with structural rearrangements of the Q arm of chromosome 3. Br. J. Haematol 1993; 83: 158–165
   PubMed Web of Science ®Google Scholar
• Bellomo M.J., Parlier V., Muhlematter D., Grab J.P., Beris P. Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome. Cancer Genetics and Cytogenetics 1992; 59: 138–160
   PubMed Web of Science ®Google Scholar
• Novitzky N., Hallett J., Jacobs P. Chromosomal abnormalities, elevated platelet count and thrombotic complications in megakaryoblastic leukaemia. Br. J. Haematol. 1991; 71: 245–246
   Web of Science ®Google Scholar
• Sundareshan T.S., Augustus M., Yasha T.C., LakshmiDevi V., Bapsy P.P. Paracentric inv(3) (q21q26) in acute myeloblasts leukemia (M2) with normal thrombopoiesis. Cancer Genetics and Cytogenetics 1992; 59: 93–94
   PubMed Web of Science ®Google Scholar
• Fichelson S., Dreyfus F., Berger R., Melle J., Bastard C., Miclea J.M., Gisselbrecht S. Evi-I expression in leukemic patients with rearrangements of the 3q25-q28 chromosomal region. Leukemia 1992; 6: 93–99
   PubMed Web of Science ®Google Scholar
• Morishita K., Parganas E., Willman C.L., Whittaker M.H., Drabkin H., Oval J., Taetle R., Valentine M.B., Ihle J. Activation of EVIl gene expression in human acute myelogenous leukemias by translocations spanning 300–400 kilobases on chromosome band 3q26. Proc. Natl. Acad. Sci. USA 1992; 89: 3937–3941
   PubMed Web of Science ®Google Scholar
• Verma R.S., da Costa M., Gogineni S.K., Palermo G. New translocation involving homologous chromosome 3 in acute myelogenous leukemia (M2). Am. J. Hematol. 1993; 42: 398–399
   PubMed Web of Science ®Google Scholar
• Fourth International Workshop of Chromosomes in Leukemia, 1982. Clinical significance of chromosomal abnormalities in acute nonlymphocytic leukemia. Cancer Genetics and Cytogenetics 1984; 11: 332–350
   PubMedGoogle Scholar
• LeBeau M.M., Albain K.S., Larson R.A., Vardiman J.W., Davis E.M., Blough R.R., Golomb H.M., Rowley J.D. Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: Further evidence for characteristic abnormalities of chromosomes no. 5 and 7. J. Clin. Oncol. 1986; 4: 325–345
   PubMed Web of Science ®Google Scholar
• Abe Y., Muta K., Yufu Y., Takahira H., Nishimura J., Nawata H. The transferring receptor system is not involved in the pathogenesis of hematological disorders with 3q inversion. Am. J. Hematol. 1990; 33: 215–219
   PubMed Web of Science ®Google Scholar
• Oval J., Smedsrud M., Taetle R. Expression and regulation of the Evi-1 gene in the human factor-dependent leukemia cell line, UCSD/AML1. Leukemia 1992; 6: 446–451
   PubMed Web of Science ®Google Scholar
• Levy E.R., Parganas E., Morishita K., Fichelson S., James L., Oscier D., Gisselbrecht S., Ihle J.N., Buckle V.J. DNA rearrangements proximal to the EVI1 locus associated with the 3q21q26 syndrome. Blood 1994; 83: 1348–1354
   PubMed Web of Science ®Google Scholar
• Matsugi T., Morishita K., Ihle J.N. Identification, nuclear localization, and DNA-binding activity of the zinc finger protein encoded by the Evi-1 myeloid transforming gene. Molecular and Cellular Biol. 1990; 10: 1259–1264
   Web of Science ®Google Scholar
• Rabbitts T.H. Translocation, master genes, and differences between the origins of acute and chronic leukemias. Cell 1991; 67: 641–644
   PubMed Web of Science ®Google Scholar
• Lapidot-Lifson Y., Prody C.A., Ginzberg D., Meytes D., Zakut H., Soreq H. Co-amplification of human acetylcholinesterase and butylcholinesterase genes in blood cells: correlation with various leukemias and abnormal megakaryocytopoiesis. Proc. Natl. Acad. Sci. USA 1989; 86: 4715–4717
   PubMed Web of Science ®Google Scholar
• Ayraud N., Donzeau M., Raynaud S., Lambert J.-C. Cytogenetic study of 88 cases of refractory anemia. Cancer Genetics and Cytogenetics 1983; 8: 243–248
   PubMed Web of Science ®Google Scholar
• Moir D.J., Jones P.A.E., Pearson J., Duncan J.R., Cook P., Buckle V.J. A new translocation, t(1;3) (p36;q21), in myelodysplastic disorders. Blood 1984; 64: 553–555
   PubMed Web of Science ®Google Scholar
• Bloomfield C.D., Garson O.M., Volin L., Knuutila S., de la Chapelle A. t(1;3) (p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic-clinicopathologic association. Blood 1985; 66: 1409–1413
   PubMed Web of Science ®Google Scholar
• Bloomfield C.D., Garson O.M., Volin L., Knuutila S., de la Chapelle A. letter to the editor. Blood 1986; 68: 320–323
   PubMedGoogle Scholar
• Najfeld V., Coyle T., Berk P.D. Transformation of polycythemia vera to acute nonlymphocytic leukemia accompanied by t(1;3) (p36;q21) karyotype. Cancer Genetics and Cytogenetics 1988; 33: 193–200
   PubMed Web of Science ®Google Scholar
• Iselius L., Hast R., Ost A., Kinell C. Translocation t(1;3) (p36;q21) in chronic myelomonocytic leukaemia. Br. J. Haematol. 1989; 72: 109–110
   PubMed Web of Science ®Google Scholar
• Marsden K.A., Pearse A.M., Collins F.F., Ford D.S., Heard S., Kimber R.I. Acute leukemia with t(1;3) (p36;q21), evolution to t(1;3) (p36;q21), t(14;17) (q32; q21), and loss of red cell A and Leb antigens. Cancer Genetics and Cytogenetics 1992; 64: 80–85
   PubMed Web of Science ®Google Scholar
• Welborn J.L., Lewis J.P., Jenks H., Walling P. Diagnostic and prognostic significance of t(1;3) (p36;q21) in the disorders of hematopoiesis. Cancer Genetics and Cytogenetics 1987; 28: 277–285
   PubMed Web of Science ®Google Scholar
• Berger R., Bernheim A., Flandrin G., Dresch C., Najean Y. Cytogenetic studies on acute nonlymphocytic leukemias following polycythemia vera. Cancer Genetics and Cytogenetics 1984; 11: 441–451
   PubMed Web of Science ®Google Scholar
• Cambrin G.R., Mecucci C., Van Orshoven A., Tricot G., Van Den Berghe H. Translocation t(1;3) (p36;q21) in malignant myeloid stem cell disorders. Cancer Genetics and Cytogenetics 1986; 22: 75–81
   PubMed Web of Science ®Google Scholar
• Oshimura M., Hayata I., Kakati S., Sandberg A.A. Chromosomes and causation of human cancer and leukemia. Banding studies in acute myeloblasts leukemia (AML). Cancer 1976; 38: 748–761
   PubMed Web of Science ®Google Scholar
• Raimondi S.C., Dube I.D., Valentine M.B., Mirro J., Jr, Watt H.J., Larson R.A., Bitter M.A., Lebeau M.M., Rowley J.D. Clinicopathologic manifestations and breakpoints of the t(3;5) in patients with acute nonlymphocytic leukemia. Leukemia 1989; 3: 42–47
   PubMed Web of Science ®Google Scholar
• Billstrom R., Heim S., Kristoffersson U., Mandahl N., Mitelman F. Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute leukemia with Sweet's syndrome. Eur. J. Haematol. 1990; 45: 150–152
   PubMed Web of Science ®Google Scholar
• McCarthy C.M., Cobcroft R.C., Harris M.G., Scott D.C. Sweet's syndrome, acute leukemia and t(3;5). Cancer Genetics and Cytogenetics 1987; 28: 87–91
   PubMed Web of Science ®Google Scholar
• Morishita K., Parganas E., Bartholomew C., Sacchi N., Valentine M.B., Raimondi S.C., LeBeau M.M., Ihle J.N. The human Evi-1 gene is located on chromosome 3q24-q28 but is not rearranged in three cases of acute nonlymphocytic leukemias containing t(3;5) (q25;q34) translocations. Oncogene Res. 1990; 5: 221–231
   PubMedGoogle Scholar
• Morris S.W., Foust J.T., Valentine M.B., Roberts W.M., Shapiro D.N., Look A.T. Sublocalization of the chromosome 5 breakpoint of the 3;5 translocation in myelodysplastic syndromes and acute myeloid leukemia. Genes Chromosomes and Cancer 1992; 5: 385–391
   PubMed Web of Science ®Google Scholar
• Armstrong E., Kastury K., Aprelikova O., Bullrich F., Nezelof C., Gogusev J., Wasmuth J.J., Alitalo K., Morris S., Huebner K. FLT4 receptor tyrosine kinase gene mapping to chromosome band 5q35 in relation to the t(2;5), t(5;6), and t(3;5) translocations. Genes Chromosomes and Cancer 1993; 7: 144–151
   PubMed Web of Science ®Google Scholar
• Mecucci C., Michaux J-L., Broechaert-Van Orshoven A., Symann M., Van Den Berghe H. Translocation t(3;17) (q26;q22): a marker of acute disease in myeloproliferative disorders. Cancer Genetics and Cytogenetics 1984; 12: 111–119
   PubMed Web of Science ®Google Scholar
• Mugneret F., Solary E., Favre B., Caillot D., Sidaner I., Guy H. New case of t(3;17) (q26;q22) as an additional change in a Philadelphia-positive chronic myelogeneous leukemia in acceleration. Cancer Genetics and Cytogenetics 1992; 60: 90–92
   PubMed Web of Science ®Google Scholar
• Rubin C.M., Larson R.A., Bitter M.A., Carrino J.J., LeBeau M.M., Diaz M.O., Rowley J.D. Association of a chromosomal 3;21 translocation with the blast phase of chronic myelogenous leukemia. Blood 1987; 70: 1338–1342
   PubMed Web of Science ®Google Scholar
• Aventin A., Mecucci C., Van Den Berghe H. (letter) Blastic phase of Ph1 -positive chronic myeloid leukemia and t(3;21). Blood 1988; 72: 369
   PubMed Web of Science ®Google Scholar
• Aventin A., Viaplana J., Zuazu I., Brunet S., Pujol-Moix N. (letter) Philadelphia-positive chronic myeloid leukemia with translocation t(3;21). Cancer Genetics and Cytogenetics 1988; 35: 133–134
   PubMed Web of Science ®Google Scholar
• Diez-Martin J.L., Dewald G.W., Pierre R.V. Possible cytogenetic distinction between lymphoid and myeloid blast crisis in chronic granulocytic leukemia. Am. J. Hematol. 1988; 27: 194–203
   PubMed Web of Science ®Google Scholar
• Coyle T., Najfeld V. Translocation (3;21) in Philadelphia chromosome-positive chronic myeloid leukemia prior to the onset of blast crisis. Am. J. Hematol. 1988; 27: 56–57
   PubMed Web of Science ®Google Scholar
• Thompson P.W., Whittaker J.A. Translocation 3;21 in Philadelphia chromosome positive chronic myeloid leukemia at diagnosis. Cancer Genetics and Cytogenetics 1989; 39: 143–146
   PubMed Web of Science ®Google Scholar
• Lafage-Pochitaloff-Huvale M., Sainty D., Adriaanssen H.J., Lopez M., Maraninchi D., Simonetti J., Mannoni P., Carcassonne Y., Hagemeijer A. Translocation (3;21) in Philadelphia positive chronic myeloid leukemia: High resolution chromosomal analysis and immunological study on five new cases. Leukemia 1989; 3: 554–559
   PubMed Web of Science ®Google Scholar
• Nucifora G., Birn D.J., Espinosa R., Erickson P., LeBeau M.M., Roulston D., McKeithan T.W., Drabkin H., Rowley J.D. Involvement of the AML1 gene in the t(3;21) in therapy-related leukemia and in chronic myeloid leukemia in blast crisis. Blood 1993; 81: 2728–2734
   PubMed Web of Science ®Google Scholar
• Rubin C.M., Larson R.A., Anastasi J., Winter J.N., Thangavelu M., Vardiman J.W., Rowley J.D., Le Beau M.M. t(3;21) (q26;q22): A recurring chromosomal abnormality in therapy-related myelodysplastic syndrome and acute myeloid leukemia. Blood 1990; 76: 2594–2598
   PubMed Web of Science ®Google Scholar
• Akahoshi M., Oshimi K., Mizoguchi H., Okada M., Enomoto Y., Watanabe Y. Myeloproliferative disorders terminating in acute megakaryoblastic leukemia with chromosome 3q26 abnormality. Cancer 1987; 60: 2654–2661
   PubMed Web of Science ®Google Scholar
• Dastugue N., Pris J., Colombies P. Translocation t(3;21) (q26;q22) in acute myeloblasts leukemia secondary to polycythemia vera. Cancer Genetics and Cytogenetics 1990; 44: 275–276
   PubMed Web of Science ®Google Scholar
• Erickson P., Fao J., Chang K.-S., Look T., Whisenant E., Raimondi S., Lasher R., Turjillo J., Rowley J., Drabkin H. Identification of breakpoints in t(8;21) AML and isolation of a fusion transcript with similarity to Drosophila segmentation gene runt. Blood 1992; 80: 1825–1831
   PubMed Web of Science ®Google Scholar
• Nucifora G., Begy C.R., Erickson P., Drabkin H.A., Rowley J.D. The 3;21 translocation in myelodysplasia results in a fusion transcript between the AMLl and the gene for EAP, a highly conserved protein associated with the Epstein-Barr virus small RNA EBER 1. Proc. Natl. Acad. Sci. USA 1993; 90: 7784–7788
   PubMed Web of Science ®Google Scholar