Advertisement
Sco| Volume 114, ISSUE 2, P159-161, October 15, 1999

Download started.

Ok

Translocation (12;17)(q13;q23) in de Novo Acute Myeloid Leukemia with Trilineage Myelodysplasia

      Abstract

      12q13 abnormalities have been reported to be associated with a variety of benign and malignant solid tumors. Recently, they have been shown to be a nonrandom karyotypic change in acute myeloid leukemia. We report a case of de novo acute myeloid leukemia with trilineage myelodysplasia showing t(12;17)(q13;q23) as the sole chromosomal abnormality. A review of the literature indicates that 12q13 translocation in acute myeloid leukemia is often associated with concomitant dysmyelopoietic changes. There is also evidence to suggest that 12q13 translocation occurs more frequently in acute myeloid leukemia with a prior history of mutagenic exposure or karyotypic indicators of secondary leukemia.
      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Cancer Genetics
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Brito-Babapulle F.
        • Catovsky D.
        • Galton D.A.G.
        Clinical and laboratory features of de novo acute myeloid leukaemia with trilineage myelodysplasia.
        Br J Haematol. 1987; 66: 445-450
        • Brito-Babapulle F.
        • Catovsky D.
        • Galton D.A.G.
        Myelodysplastic relapse of de nova acute myeloid leukaemia with trilineage myelodysplasia.
        Br J Haematol. 1988; 68: 411-415
        • Tamura S.
        • Kanamaru A.
        • Takemoto Y.
        • Kakishita E.
        • Nagai K.
        Clonal evolutions during long-term cultures of bone marrow from de nove acute leukaemia with trilineage myelodysplasia and with myelodysplastic remission marrow.
        Br J Haematol. 1993; 84: 219-226
        • Bennett J.M.
        • Catovsky D.
        • Daniel M.T.
        • Flandrin G.
        • Galton D.A.G.
        • Gralnick H.R.
        • Sultan C.
        Proposed revised criteria for the classification of acute myeloid leukaemia.
        Ann Intern Med. 1985; 103: 626-629
        • Becher R.
        • Haas O.A.
        • Graeven U.
        • Bettelheim U.
        • Ambros P.
        • Fridrik M.
        • Schaefer U.W.
        • Schmidt C.G.
        Translocation t(8;16) in acute monocytic leukemia.
        Cancer Genet Cytogenet. 1988; 34: 265-271
        • Seyer M.M.
        • Ritterbach J.
        • Creutzig U.
        • Gnekow A.K.
        • Gobel A.K.
        • Graf N.
        • Reiter A.
        • Lampert F.
        • Harbott J.
        12q13, a new recurrent breakpoint in acute nonlymphoblastic leukemia.
        Cancer Genet Cytogenet. 1995; 80: 23-28
        • Raanani P.
        • Rosner E.
        • Bercowicz M.
        • Ben-Bassat I.
        t(12;20)(q13;p11.2).
        Cancer Genet Cytogenet. 1996; 89: 118-119
        • Perkins D.
        • Brennan S.
        • Carstairs K.
        • Bailey D.
        • Pantalony D.
        • Poon A.
        • Fernandes B.
        • Dube I.
        Regional cancer cytogenetics.
        Cancer Genet Cytogenet. 1997; 96: 64-80
        • Wong K.F.
        • Kwong Y.L.
        • So C.C.
        De novo AML with trilineage myelodysplasia and a novel translocation t(11;12)(p15;q13).
        Cancer Genet Cytogenet. 1998; 100: 49-51
        • Yamamoto K.
        • Hamaguchi H.
        • Nagata K.
        • Kobayashi M.
        • Tanimoto F.
        • Taniwaki M.
        Establishment of a novel human acute myeloblastic leukemia cell line (YNH-1) with t(16;21),t(1;16) and 12q13 translocations.
        Leukemia. 1997; 11: 599-608
        • Fitzgerald P.H.
        • Morris C.M.
        • Fraser G.J.
        • Giles L.M.
        • Hamer J.W.
        • Heaton D.C.
        • Beard M.E.J.
        Nonrandom cytogenetic changes in New Zealand patients with acute myeloid leukemia.
        Cancer Genet Cytogenet. 1983; 8: 51-66
        • Raidmondi S.C.
        • Kalwinsky D.K.
        • Hayashi Y.
        • Behm F.G.
        • Mirro J.J.
        • Williams D.L.
        Cytogenetics of childhood acute nonlymphocytic leukemia.
        Cancer Genet Cytogenet. 1989; 40: 13-27
        • Rowley J.D.
        • Golomb H.M.
        • Vardiman J.W.
        Nonrandom chromosome abnormalities in acute leukemia and dysmyelopoietic syndromes in patients with previously treated malignant disease.
        Blood. 1981; 58: 759-767
        • Pedersen-Bjergaard J.
        • Philip P.
        • Pedersen N.T.
        • Hou-jensen K.
        • Svejgaard A.
        • Jensen G.
        • Nissen N.I.
        Acute nonlymphocytic leukemia, preleukemia, and acute myeloproliferative syndrome secondary to treatment of other malignant disease II.
        Cancer. 1984; 54: 452-462
        • Bitter M.A.
        • Neilly M.E.
        • Le Beau M.M.
        • Pearson M.G.
        • Rowley J.D.
        Rearrangements of chromosome 3 involving bands 3q21 and 3q26 are associated with normal or elevated platelets counts in acute nonlymphocytic leukemia.
        Blood. 1985; 66: 1362-1370
        • Paietta E.
        • Papenhausen P.
        • Gucalp R.
        • Wiernik P.H.
        Translocation t(12;19)(q13;q13.3), a new recurrent abnormality in acute nonlymphocytic leukemia with atypical erythropoiesis.
        Cancer Genet Cytogenet. 1988; 34: 19-23
        • Brusamolino E.
        • Orlandi E.
        • Morra E.
        • Bernasconi P.
        • Pagnucco G.
        • Columbo A.
        • Lazzarino M.
        • Bernasconi C.
        Hematologic and clinical features of patients with chromosome 5 monosomy or deletion (5q).
        Med Pediatr Oncol. 1998; 16: 88-94
        • Badia L.
        • Alvarez M.A.
        • Palau F.
        • Prieto F.
        Translocation (12;14)(q13;q32) in myelodysplastic syndrome.
        Cancer Genet Cytogenet. 1993; 65: 76-78
        • Ohjimi Y.
        • Iwasaki H.
        • Kaneko Y.
        • Ishiguro M.
        • Ohgami A.
        • Fujita C.
        • Shinohara N.
        • Yoshitake K.
        • Kikuchi M.
        Chromosome abnormalities in liposarcomas.
        Cancer Genet Cytogenet. 1992; 64: 111-117
        • Roberts P.
        • Browne C.F.
        • Lewis I.J.
        • Bailey C.C.
        • Spicer R.D.
        • Williams J.
        • Batcup G.
        12q13 abnormality in rhabdomyosarcoma, a nonrandom occurrence?.
        Cancer Genet Cytogenet. 1992; 60: 135-140
        • Mertens F.
        • Jonsson K.
        • Willen H.
        • Rydholm A.
        • Eriksson L.
        • Olsson-Sandin G.
        • Mitelman F.
        • Mandahl N.
        Chromosome rearrangements in synovial chondromatous lesions.
        Br J Cancer. 1996; 74: 251-254
        • Willen H.
        • Akerman M.
        • Dal Cin P.
        • De Wever I.
        • Fletcher C.D.
        • Mandahl N.
        • Mertens N.
        • Mitelman F.
        • Rosai J.
        • Rydholm A.
        • Sciot R.
        • Tallini G.
        • Van den Berghe H.
        • Vanni R.
        Comparison of chromosomal patterns with clinical features in 165 lipomas.
        Cancer Genet Cytogenet. 1998; 102: 46-49
        • Mtichell E.L.
        • White G.R.
        • Santibanez-Koref M.F.
        • Varley J.M.
        • Heighway J.
        Mapping of gene loci in the q13–q15 region of chromosome 12.
        Chromosome Res. 1995; 3: 261-262
        • Merup M.
        • Juliusson G.
        • Wu X.
        • Jansson M.
        • Stellan B.
        • Rasool O.
        • Roijer E.
        • Stenman G.
        • Gahrton G.
        • Einhorn S.
        Amplification of multiple regions of chromosome 12, including 12q13–15, in chronic lymphocytic leukaemia.
        Eur J Haematol. 1997; 58: 174-180
        • Rao P.H.
        • Houldsworth J.
        • Dyomina K.
        • Parsa N.Z.
        • Cigudosa J.C.
        • Louie D.C.
        • Popplewell L.
        • Offit K.
        • Jhanwar S.C.
        • Chaganti R.S.
        Chromosomal and gene amplification in diffuse large B-cell lymphoma.
        Blood. 1998; 92: 234-240
        • Le Beau M.M.
        • Rowley J.D.
        Heritable fragile sites in cancer.
        Nature. 1984; 308: 607-608
        • Mitelman F.
        • Nilsson P.G.
        • Brandt L.
        • Alimena G.
        • Gastaldi R.
        • Dallapiccola B.
        Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia.
        Cancer Genet Cytogenet. 1981; 4: 197-214
        • Kantarjian H.M.
        • Keating M.J.
        Therapy-related leukemia and myelodysplastic syndrome.
        Sem Oncol. 1987; 14: 435-443
        • Minelli A.
        • Piantanida M.
        • Maserati E.
        • Campagnoli E.
        • Pasquali F.
        • Danesino C.
        Gene dosage effect in acquired monosomy 7.
        Genes Chromosom Cancer. 1990; 1: 216-220