Advertisement
Original articles| Volume 114, ISSUE 2, P121-125, October 15, 1999

Download started.

Ok

Jumping Translocations Involving 11q in a Non-Hodgkin Lymphoma

      Abstract

      This paper presents the results of a cytogenetic analysis in an 11-year-old boy with non-Hodgkin lymphoma. The investigation was performed on slides obtained from short-term culture of lymph node cells. The analyses revealed an abnormal clone with loss of the Y, gain of an X chromosome, t(3;22), trisomy 11, and three cytogenetically-related subclones with jumping translocations involving 11q13 as the common breakpoint region. This region is an unusual site of chromosome breakage in jumping translocations, and has not been reported thus far. Contrary to most published reports, the jumping translocation in our patient is associated with long survival.
      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

        • Hoffschir F.
        • Ricoul M.
        • Lemieux N.
        • Estrade S.
        • Cassingena R.
        • Dutrillaux B.
        Jumping translocations originate clonal rearrangements in SV40-transformed human fibroblasts.
        Int J Cancer. 1992; 52: 130-136
        • Von Ballestrem C.L.
        • Boavida M.G.
        • Zuther C.
        • Carreiro M.H.
        • David D.
        • Gal A.
        • Schwinger E.
        Jumping translocation in a phenotypically normal female.
        Clin Genet. 1996; 49: 156-159
        • Duval E.
        • van den Enden A.
        • Vanhaesebrouck P.
        • Speleman F.
        Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
        Am J Med Genet. 1994; 52: 214-217
        • Gray B.A.
        • Bent-Williams A.
        • Wadsworth J.
        • Maiese R.L.
        • Bhatia A.
        • Zori R.T.
        Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma.
        Cancer Genet Cytogenet. 1997; 98: 20-27
        • Roland B.
        • Pinto A.
        • Bowen T.
        Jumping translocation involving 1q in a small noncleaved cell lymphoma.
        Am J Hum Genet Suppl. 1992; 51: A69
        • Sawyer R.J.
        • Swanson C.M.
        • Koller A.M.
        • North P.E.
        • Ross S.W.
        Centromeric instability of chromosome 1 resulting in multibranched chromosomes, telomeric fusions, and “jumping” translocations of 1q in a human immunodeficiency virus-related non-Hodgkin's lymphoma.
        Cancer. 1995; 76: 1238-1244
        • Wlodarska I.
        • Mecucci C.
        • De Wolf-Peeters C.
        • Verhoef G.
        • Weier H.U.
        • Cassiman J.J.
        • Van Den Berghe H.
        “Jumping” translocation of 9q in a case of follicular lymphoma.
        Cancer Genet Cytogenet. 1994; 76: 140-144
        • Whang-Peng J.
        • Lee E.C.
        • Sieverts H.
        • Magrath I.T.
        Burkitt's lymphoma in AIDS.
        Blood. 1984; 63: 818-822
        • Shikano T.
        • Arioka H.
        • Kobayashi R.
        • Naito H.
        • Ishikawa Y.
        Jumping translocations of 1q in Burkitt lymphoma and acute nonlymphocytic leukemia.
        Cancer Genet Cytogenet. 1993; 71: 22-26
        • Fitzgerald P.H.
        • Morris C.M.
        Telomeric association of chromosomes in B-cell lymphoid leukemia.
        Hum Genet. 1984; 67: 385-390
        • Shippey C.A.
        • Layton M.
        • Secker-Walker L.M.
        Leukemia characterized by multiple sub-clones with unbalanced translocations involving different telomeric segments.
        Genes Chromosom Cancer. 1990; 2: 14-17
        • Najfeld V.
        • Hauschildt B.
        • Scalise A.
        • Gattani A.
        • Patel R.
        • Ambinder E.P.
        • Silverman L.R.
        Jumping translocations in leukemia.
        Leukemia. 1995; 9: 634-639
        • Huret J.L.
        • Tanzer J.
        • Guilhot F.
        • Frocrain-Herchkovitch C.
        • Savage R.K.
        Karyotype evolution in the bone marrow of a patient with Fanconi anemia.
        Cytogenet Cell Genet. 1988; 48: 224-227
        • Raimondi S.C.
        • Ragsdale S.T.
        • Behm F.
        • Rivera G.
        • Williams D.L.
        Multiple telomeric associations of a trisomic whole q arm of chromosome 1 in a child with acute lymphoblastic leukemia.
        Cancer Genet Cytogenet. 1987; 24: 87-93
        • Reis M.D.
        • Dube I.D.
        • Pinkerton P.H.
        • Chen-Lai J.
        • Robinson J.B.
        • Klock R.J.
        • Senn J.S.
        “Jumping” translocations involving band 3q13.3 in a case of acute monocytic leukemia.
        Cancer Genet Cytogenet. 1991; 51: 189-194
        • Ben-Neriah S.
        • Abramov A.
        • Lerer I.
        • Polliack A.
        • Leizerowitz R.
        • Rabinowitz R.
        • Abeliovich D.
        “Jumping translocation” in a 17-month-old child with mixed-lineage leukemia.
        Cancer Genet Cytogenet. 1991; 56: 223-229
        • Aledo R.
        • Aurias A.
        • Chretien B.
        • Dutrillaux B.
        Jumping translocation of chromosome 14 in a skin squamous cell carcinoma from a xeroderma pigmentosum patient.
        Cancer Genet Cytogenet. 1988; 33: 29-33
        • Seabright M.
        The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man.
        Chromosoma. 1977; 36: 204-210
      1. ISCN (1991): Guidelines for Cancer Cytogenetics, Supplement to An International System for Human Cytogenetic Nomenclature. F Mitelman, ed. S. Karger, Basel.

        • Offit K.
        • Jhanwar S.
        • Ebrahim S.A.D.
        • Filippa D.
        • Clarkson B.D.
        • Chaganti R.S.K.
        t(3;22)(q27;q11).
        Blood. 1989; 74: 1876-1879
        • Mikraki V.
        • Jhanwar S.C.
        • Filippa D.A.
        • Wollner N.
        • Chaganti R.S.K.
        Distinct patterns of chromosome abnormalities characterize childhood non-Hodgkin's lymphoma.
        Br J Haematol. 1992; 80: 15-20
        • Shikano T.
        • Ishikawa Y.
        • Naito H.
        • Kobayashi R.
        • Nakadate H.
        • Hatae Y.
        • Takeda T.
        Cytogenetic characteristics of childhood non-Hodgkin's lymphoma.
        Cancer. 1992; 70: 714-719
        • Prasad R.K.
        • Filippa D.A.
        • Richardson M.E.
        • Jhanwar S.C.
        • Chaganti S.R.
        • Koziner B.
        • Clarkson B.D.
        • Lieberman P.H.
        • Chaganti R.S.K.
        Cytogenetic and histologic correlations in malignant lymphoma.
        Blood. 1987; 69: 97-102
        • Hecht F.
        • Sutherland G.R.
        Fragile sites and cancer breakpoints.
        Cancer Genet Cytogenet. 1984; 12: 179-181
        • De Boer C.J.
        • Loyson S.
        • Kluin P.M.
        • Kluin-Nelemans H.C.
        • Schuuring E.
        • Van Krieken J.H.J.M.
        Multiple breakpoints within the BCL-1 locus in B-cell lymphoma.
        Cancer Res. 1993; 53: 4148-4152
        • Rimokh R.
        • Berger F.
        • Delsol G.
        • Charrin C.
        • Bertheas M.F.
        • Ffrench M.
        • Garoscio M.
        • Felman P.
        • Coiffier B.
        • Bryon P.A.
        • Rochet M.
        • Gentilhomme O.
        • Germain D.
        • Magaud J.P.
        Rearrangement and overexpression of the BLC-1/PRAD-1 gene in intermediate lymphocytic lymphoma and in t(11q13)-bearing leukemias.
        Blood. 1993; 81: 3063-3067
        • Mamaeva S.E.
        • Mamaev N.N.
        • Jartseva N.M.
        • Belyaeva L.V.
        • Scherbakova E.G.
        Complete or partial trisomy for the long arm of chromosome 1 in patients with various hematologic malignancies.
        Hum Genet. 1983; 63: 107-112