31
Views
6
CrossRef citations to date
0
Altmetric
Original Article

HRX Gene Rearrangement in Secondary Acute Lymphoblastic Leukemia

, , &
Pages 391-399 | Received 15 Jul 1994, Published online: 01 Jul 2009

References

  • Sait S. N., Raza A., Sandberg A. A. A t(1;11) in acute nonlymphocytic leukemia FAB type M4. Cancer Genet. Cytogenet. 1987; 24: 181–183
  • Feder M., Finan J., Besa E., Nowell P. A 2p;11q chromosome translocation in dysmyelopoietic preleukemia. Cancer Genet. Cytogenet. 1985; 15: 143–150
  • Derre J., Cherif D., Le Coniat M., Julier C., Berger R. In situ hybridization ascertains the presence of a translocation 1(2;11) in an acute monocytic leukemia. Genes Chromosomes Cancer 1990; 32: 341–344
  • Abe R., Ryan D., Cecalpo A., Cohen H., Sandberg A. A. Cytogenetic findings in congenital leukemia: case report and review of the literature. Cancer Genet. Cytogenet. 1983; 9: 139–144
  • Hagemeijer A., Hählen K., Sizoo W., Abels J. Translocation (9;11)(p21;q23) in three cases of acute monoblastic leukemia. Cancer Genet. Cytogenet. 1982; 5: 95–105
  • Kaneko Y., Maseki N., Takasaki N., Sakurai M., Hayashi Y., Nakazawa S., Mori T., Sakurai M., Takeda T., Shikano T., Hiyoshi Y. Clinical and hematologic characteristics in acute leukemia with 11q23 translocation. Blood 1986; 67: 484–491
  • Raimondi S. C., Peiper S. C., Kitchingman G. R., Behm F. G., Williams D. L., Hancock M. L., Mirro J., Jr. Childhood acute lymphoblastic leukemia with chromosomal breakpoints at 11q23. Blood 1989; 73: 1627–1634
  • Pui C.-H. Acute leukemias with the t(4;11)(q21;q23). Leukemia and Lymphoma 1992; 7: 173–179
  • Pui C.-H., Carroll A. J., Raimondi S. C., Shuster J. J., Crist W. M., Pullen D. J. Childhood acute lymphoblastic leukemia with the t(4;11)(q21;q23); An update. Blood 1994; 83: 2384–2385
  • Bloomfield C. D., Seeker-Walker L. M., Goldman A. I., Van Den Berghe H., de la Chapelle A., Ruutu T., Alimena G., Garson O. M., Golomb H. M., Rowley J. D., Kaneko Y., Whang-Peng J., Prigogina E., Philip P., Sandberg A. A., Lawler S. D., Mitelman F. Six-year follow-up of the clinical significance of karyotype in acute lymphoblastic leukemia. Cancer Genet. Cytogenet. 1989; 40: 171–185
  • Arthur D. C., Bloomfield C. D., Lindquist L. L., Nesbit M. E., Jr. Translocation 4;11 in acute lymphoblastic leukemia: clinical characteristics and prognostic significance. Blood 1982; 59: 96–99
  • Mirro J., Kitchingman G., Williams D., Lauzen G. J., Lin C.-C, Callihan T., Zipf T. F. Clinical and laboratory characteristics of acute leukemia with the 4;11 translocation. Blood 1986; 67: 689–697
  • Nagasaka M., Maeda S., Maeda H., Chen H.-L., Kita K., Mabuchi O., Misu H., Matsuo T., Sugiyama T. Four cases of t(4;11) acute leukemia and its myelomonocytic nature in infants. Blood 1983; 61: 1174–1181
  • Parkin J. L., Arthur D. C., Abramson C. S., McKenna R. W., Kersy J. H., Heideman R. L., Brunning R. D. Acute leukemia associated with the t(4;11) chromosomal rearrangement: Ultrastructural and immunologic characteristics. Blood 1982; 60: 1321–1331
  • Crist W. M., Cleary M. L., Grossi C. E., Prasthofer E. F., Heggie G. D., Omura G. A., Carroll A. J., Link M. P., Sklar J. Acute leukemias associated with the 4; 11 chromosome translocation have rearranged immunoglobulin heavy chain genes. Blood 1985; 66: 38–45
  • Sandoval C., Head D. R., Mirro J., Jr., Behm F. G., Ayers G. D., Raimondi S. C. Translocation t(9;11)(p21;q23) in pediatric de novo and secondary acute myeloblasts leukemia. Leukemia 1992; 6: 513–519
  • Dewald G. W., Morrison-De Lap S. J., Schuchard K. A., Spurbeck J. L., Pierre R. V. A possible specific chromosome marker for monocytic leukemia. Three more patients with t(9;11)(p21;q23) and another with t(11;17)(q24;q21), each with acute monoblastic leukemia. Cancer Genet. Cytogenet. 1983; 8: 203–212
  • Pui C.-H., Raimondi S. C., Murphy S. B., Ribeiro R. C., Kalwinsky D. K., Dahl G. V., Crist W. M., Williams D. L. An analysis of leukemic cell chromosomal features in infants. Blood 1987; 69: 1289–1293
  • Williams D. L., Look A. T., Melvin S. L., Roberson P. K., Dahl G., Flake T., Stass S. New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemia. Cell 1984; 36: 101–109
  • Ball E. D., Davis R. B., Griffin J. D., Mayer R. J., Davey F. R., Arthur D. C., Wurster-Hill D., Noll W., Flghetany M. T., Allen S. L., Rai K., Lee E. J., Schiffer C. A., Bloomfield C. D. Prognostic value of lymphocyte surface markers in acute myeloid leukemia. Blood. 1991; 77: 2242–2250
  • Van Lierde S., Mecucci C., Casteels-van Daele M., van den Berghe H. Lineage switch and translocation t(9;11) in acute leukemia. Am. J. Pediatr. Hematol. Oncol. 1989; 11: 20–22
  • Ackland S. P., Westbrook C. A., Diaz M. O., Le Beau M. M., Rowley J. D. Evidence favoring lineage fidelity in acute nonlymphocytic leukemia: Absence of immunoglobulin gene rearrangements in FAB types M4 and M5. Blood 1987; 69: 87–91
  • Lorenzana A. N., Rubin C. M., Le Beau M. M., Nachman J., Connoly P., Subramanian U., Johnson F. L., McKeithan T. W. Immunoglobulin genes rearrangements in acute lymphoblastic leukemia with the 9; 11 translocation. Genes Chromosomes Cancer 1991; 3: 74–77
  • Hayashi Y., Kobayashi Y., Hirai H., Hanada R., Yamamoto K., Abe T., Sugita K., Nakazawa S., Suetake N., Hoshino H., Kuroume T., Bessho F., Hayakawa H., Takaku F. Immunoglobulin heavy chain gene rearrangements and mixed characteristics in acute leukemias with the 11;19 translocation. Cancer 1988; 61: 712–720
  • Huret J. L., Brizard A., Slater R., Charrin C., Bertheas M. F., Guilhot F., Hählen K., Kroes W., van Leeuwen E., School E. V. D., Beishuizen A., Tanzer J., Hagemeijier A. Cytogenetic heterogeneity in t(11;19) acute leukemia: clinical hematological and cytogenetic analyses of 48 patients-updated published cases and 16 new observations. Leukemia 1993; 7: 152–160
  • McCabe N. R., Burnett R. C., Gill H. J., Thirman M. J., Mbangkollo D., Magdalena K., Van Melle E., Ziemin-Van Der Poel S., Rowley J. D., Diaz M. O. Cloning of cDNAs of the MLL gene that detect DNA rearrangement and altered RNA transcripts in human leukemic cells with 11q23 translocation. Proc. Natl. Acad. Set. USA 1992; 89: 11794–11798
  • Gu Y., Nakamura T., Alder H., Prasad R., Canaani O., Cimino G., Croce C. M., Canaani E. The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophia trithorax, to the AF-4 gene. Cell. 1992; 71: 701–708
  • Tkachuk D. C., Kohler S., Cleary M. L. Involvement of a homologue of Drosophia Trithorax by 11q23 chromosomal translocations in acute leukemia. Cell 1992; 71: 691–700
  • Morrissey J., Tkachuk D. C., Milatovich A., Francke V., Link M., Cleary M. L. A serine/proteine-rich protein is fused to HRX in t(4;11) acute leukemias. Blood 1993; 81: 1124–1131
  • Nakamura T., Alder H., Gu Y., Prasad R., Canaani O., Kamada N., Gale R. P., Lange B., Crist W. M., Nowell P. C., Croce C. M., Canaani E. Gene on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs. Proc. Nail. Acad. Sci. USA 1993; 90: 4631–4635
  • Yamamoto K., Seto M., Komatsu H., Lida S., Akao Y., Kojima S., Kodera Y., Nakazawa S., Ariyoshi Y., Takahashi T., Ueda R. Two distinct portions of LTG19/ENL at 19p13 are involved in t(11;19) leukemia. Oncogene 1993; 8: 2617–2625
  • Hunger S. P., Sklar J., Link M. P. Acute lymphoblastic leukemia occurring as a second malignant neoplasm in childhood: re port of three cases and review of the literature. J. Clin. Oncol. 1992; 10: 156–163
  • Gill Super H. J., McCabe N. R., Thirman M. J., Larson R. A., Le Beau M. M., Pederson-Bjergaard J., Philip P., Diaz M. O., Rowley J. D. Rearrangement of the MLL gene in. therapy-related acute myelod leukemia in patients previously treated with agents targeting DNA-topoisomerase II. Blood 1993; 82: 3705–3711
  • Thirman M. J., Gill H. J., Burnett R. C., Mbangkollo D., McCabe N. R., Kobayashi H., Ziemin-Van Der Poel S., Kaneko Y., Morgan R., Sandberg A. A., Chaganti R. S. K., Larson R. A., Le Beau M. M., Diaz M. O., Rowley J. D. Rearrangement of the MLL gene in acute lymphoblastic and acute myeloid leukemias with 11q23 chromosomal translocations. N. Engl. J. Med. 1993; 329: 909–914
  • Sorensen P. H., Chen C. S., Smith F. O., Arthur D. C., Domer P. H., Bernstein I. D., Korsmeyer S. J., Hammond G. D., Kersey J. H. Molecular rearrangements of the MLL gene are present in most cases of infant acute myeloid leukemia and are strongly correlated with monocytic or myelomonocytic phenotypes. J. Clin. Invest. 1994; 93: 429–437
  • Kobayashi H., Espinosa R., III, Thirman M., Gill H. J., Fernald A. A., Diaz M. O., Le Beau M. M., Rowley J. D. Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization. Blood 1993; 82: 547–551
  • Lo Coco F., Mandelli F., Breccia M., Annino L., Guglielmi C., Petti M. C., Testi A. M., Alimena G., Croce C. M., Canaani E., Cimino G. Southern blot analysis of ALL-1 rearrangement at chromosome 11q23 in acute leukemia. Cancer Res. 1993; 53: 3800–3803
  • Ziemin-van der Poel S., McCabe N. R., Gill H. J., Espinosa R., III, Patel Y., Harden A., Rubinelli P., Smith S. D., Le Beau M. M., Rowley J. D., Diaz M. O. Identification of a gene, MLL that spans the breakpoint in 11q23 translocation associated with human leukemias. Proc. Nail. Acad. Sci. USA 1991; 88: 10735–10739
  • Corral J., Forster A., Thompson S., Lampert F., Kaneko Y., Slater R., Kroes W. G., van der Schoot C. E., Ludwig W.-D., Karpas A., Pocock C., Cotter F., Rabbitts T. H. Acute leukemias of different lineage have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation. Proc. Natl. Acad. Sci. USA 1993; 90: 8538–8542
  • Morgan G. J., Cotter F., Katz F. E., Ridge S. A., Domer P., Korsmeyer S., Wiedemann L. M. Breakpoints at 11q23 in infant leukemias with the t(11;19)(q23;p13) are clustered. Blood 1992; 80: 2172–2175
  • Kearney 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 translocation in both infant and adult acute leukemias are detected by in situ hybridization with a yeast artificial chromosome. Blood 1992; 80: 1659–1665
  • Yamamoto K., Seto M., Iida S., Komatsu H., Kamada N., Kojima S., Kodera Y., Nakazawa S., Saito H., Takahashi T., Ueda R. A reverse transcriptase-polymerase reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities. Blood 1994; 83: 2912–2921
  • Chen Z., Guidez F., Rousselot P., Agadir A., Chen S. J., Wang Z. Y., Degos L., Zelent A., Waxman S., Chomienne C. PLZF-RAR alpha fusion proteins generated from the variant t(11;17)(q23;q21) translocation in acute promyelocytic leukemia inhibit ligand-dependent transactivation of wild-type retinoic acid receptors. Proc. Natl. Acad. Sci. USA 1994; 91: 1178–1182
  • Lu D., Yunis J. J. Cloning, expression and localization of an RNA helicase gene from a human lymphoid cell line with chromosomal breakpoint 11q23.3. Nucleic Acids Res. 1992; 20: 1967–1972
  • Akao Y., Seto M., Yamamoto K., Iida S., Nakazawa S., Inazawa J., Abe T., Takahashi T., Ueda R. The RCK gene associated with t(11;14) translocation distinct from the MLL/ALL-I gene with t(4;11) and t(11;19) translocations. Cancer Res. 1992; 52: 6083–6087
  • Burnett R. C., Espinosa R. I., Shows T. B., Eddy R. L., Le Beau M. M., Rowley J. D., Diaz M. O. Molecular analysis of a t(11;14)(q23;q11) from a patient with null-cell acute lymphoblastic leukemia. Genes Chromosomes Cancer 1993; 7: 38–46
  • Kobayashi H., Espinosa R., III, 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
  • Cherif D., Der-Sarkissian H., Derré J., Tokino T., Nakamura Y., Berger R. The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11). Genes Chromosomes Cancer 1992; 4: 107–112
  • Mitani K., Sato Y., Kobayashi Y., Shibasaki Y., Kasuga M., Inaba T., Hayashi Y., Miura Y., Miyazono K., Hirai H., Urabe A., Takaku F. Heterogeneity in the breakpoints of chromosome 19 among acute leukemia patients with the t(11;19)(q23;p13) translocation. Am. J., Hematol. 1989; 31: 253–257
  • Saltman D. L., Mellentin J. D., Smith S. D., Cleary M. L. Mapping of translocation breakpoints on the short arm of chromosome 19 in acute leukemias by in situ hybridization. Genes Chromosomes Cancer 1990; 2: 259–265
  • Pui C.-H., Behm F. G., Raimondi S. C., Dodge R. K., George S., Rivera G. K., Mirro J., Jr., Kalwinsky D. K., Dahl G. V., Murphy S. B., Crist W. M., Williams D. L. Secondary acute myeloid leukemia in children treated for acute lymphoid leukemia. N. Engl. J. Med. 1989; 321: 136–142
  • Pui C.-H., Ribeiro R. C., Hancock M. L., Rivera G. K., Evans W. E., Raimondi S. C., Head D. R., Behm F. G., Mahmoud H., Sandlund J. T., Crist W. M. Acute myelod leukemia in children treated with epipodophyllotoxins for acute lymphoblastic leukemia. N. Engl. J. Med 1991; 325: 1682–1687
  • Pedersen-Bjergaad J., Philip P., Larsen S. O., Jensen G., Byrsting K. Chromosome aberrations and prognostic factors in therapy-related myelodysplasia and acute nonlymphocytic leukemia. Blood 1990; 76: 1083–1091
  • Pedersen-Bjergaard J., Philip P., Larsen S. O., Andersson M., Daugaard G., Ersbell J., Hansen S. W., Hou-Jensen K., Nielsen D., Sigsgaard T. C., Specht L., Østerlind K. Therapy-related myelodysplasia and acute myeloid leukemia. Cytogenetic characteristics of 115 consecutive cases and risk in seven cohorts of patients treated intensively for malignant disease in the Copenhagen series. Leukemia. 1993; 7: 1975–1986
  • Ratain M. J., Kaminer L. S., Bitran J. D., Larson R. A., Le Beau M. M., Skosey C., Purl S., Hoffman P. C., Wade J., Vardiman J. W., Daly K., Rowley J. D., Golomb H. M. Acute nonlymphocytic leukemia following etoposide and cisplatin combination chemotherapy for advanced non-small-cell carcinoma of the lung. Blood 1987; 70: 1412–1417
  • De Vore R., Whitlock J., Hainsworth J. D., Johnson D. H. Therapy-related acute nonlymphocytic leukemia with monocytic features and rearrangement of chromosome 11q. Ann Int Med. 1989; 110: 740–742
  • Weh H. J., Kabisch H., Landbeck G., Hossfeld D. K. Translocation (9;11)(p21;q23) in a child with acute monoblastic leukemia following 2 1/2 years after successful chemotherapy for neuroblastoma. J. Clin. Oncol. 1986; 4: 1518–1520
  • Prieto F., Palau F., Badia L., Beneyto M., Perez-Sirvent M. L. A., Castel V. 11q23 abnormalities in children with acute nonlymphocytic leukemia(M4-M5). Association with previous therapy. Cancer Genet. Cytogenet. 1990; 45: 1–11
  • Rubin C. M., Arthur D. C., Woods W. G., Lange B. J., Nowell P. C., Rowley J. D., Nachman J., Bostrom B., Baum E. S., Suarez C. R., Shah N. R., Morgan E., Maurer H. S., McKenzie S. E., Larson R. A., Le Beau M. M. Therapy-related myelodysplastic syndrome and acute myelod leukemia in children: Correlation between chromosomal abnormalities and prior therapy. Blood. 1991; 78: 2982–2988
  • Rowley J. D., Golomb H. M., Vardiman J. W. Nonrandom chromosome abnormalities in acute leukemia and dysmyelopoetic syndromes in patients with previously treated malignant disease. Blood 1981; 58: 759–767
  • Pedersen-Bjergaard J., Sigsgaard T. C, Nielsen D., Gjedde S. B., Philip P., Hansen M., Larsen S. O., Rørth M., Mouridsen H., Dombernowsky P. Acute monocytic or myelomonocytic leukemia with balanced chromosome translocations to band 11q23 after therapy with 4-epi-doxorubicin and cisplatin or cyclophosphamide for breast cancer. J. Clin. Oncol. 1992; 10: 144–1451
  • Kobayashi Y., Yang J., Shindo E., Tojo A., Tani K., Ozawa K., Asano S. HRX gene rearrangement in acute lymphoblastic leukemia after adjuvant chemotherapy of breast cancer. Blood 1993; 82: 3220–3221
  • Sugita K., Furukawa T., Tsuchida M., Okawa Y., Nakazawa S., Akatsuka J., Ohira M., Nishimura K. High frequency of etoposide(VP-16) related secondary leukemia in children with non-Hodgkin's lymphoma. Am. J. Pediatr. Hematol. Oncol 1993; 15: 99–104
  • Sandoval C., Pui C.-H., Bowman L. C., Heaton D., Hurwitz C. A., Raimondi S. C., Behm G. F., Head D. R. Secondary acute myeloid leukemia in children previously treated with alkylating agents, intercalating topoisomerase II inhibitors, and irradiation. J. Clin. Oncol. 1993; 11: 1039–1045
  • Pedersen-Bjergaard J., Philip P. Balanced translocation involving chromosome bands 11q23 and 21q22 are highly characteristic of myelodysplasia and leukemia following therapy with cytostatic agents targeting at DNA-topoisomerase II. Blood 1991; 78: 1147–1148
  • Bae Y.-S., Kawasaki I., Ikeda H., Liu L. F. Illegitimate recombination mediated by calf thymus DNA topoisomerase II in vivo. Proc. Natl. Acad. Sci. USA 1988; 85: 2076–2080
  • Negrini M., Felix C. A., Martin C., Lange B. J., Nakamura T., Canaani E., Croce C. M. Potential topoisomerase II DNA-binding site at the breakpoints of a t(9;11) chromosome translocation. Cancer Res. 1993; 53: 4489–4492
  • Weiss R. B. The anthracyclines: Will we find a better doxorubicin?. Seminars Oncol. 1992; 670–686
  • Kapelushnik J., Dubé I., Wilson P., Greenberg M. Acute lymphoblastic leukemia with t(4;11) translocation after osteogenic sarcoma. Cancer 1990; 67: 2887–2889
  • Pedersen-Bjergaard P., Rowley J. D. The balanced and unbalanced chromosome aberrations of acute myeloid leukemia may develop in different ways and may contribute differently to malignant transformation. Blood 1994; 83: 2780–2786
  • Hudson M. M., Raimondi S. C., Behm F. G., Pui C.-H. Childhood acute leukemia with t(11;19)(q23;p13). Leukemia 1991; 5: 1064–1068

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.