Inversion of chromosome 11, inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: Identification of a P1 clone spanning the 11q22 breakpoint

Genes Chromosomes and Cancer

Volumn 19, Issue 3, 1997, Pages 150-155

  Kobayashi, Hirofumi ^a   Arai, Yasyhito ^b   Hosoda, Fumie ^b   Maseki, Nobuo ^a   Hayashi, Yasuhide ^c   Eguchi, Haruhiko ^d   Ohki, Misao ^b   Kaneko, Yasuhiko ^a  

^a SAITAMA CANCER CENTER   (Japan)

^b NATIONAL CANCER CENTER RESEARCH INSTITUTE   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

^d KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOTOXIC AGENT; GYRASE INHIBITOR;

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 11Q; CHROMOSOME INVERSION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; MYELODYSPLASTIC SYNDROME; MYELOPROLIFERATIVE DISORDER; NONHODGKIN LYMPHOMA; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

ADOLESCENT; ADULT; ANEMIA, REFRACTORY, WITH EXCESS OF BLASTS; ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS; BACTERIOPHAGE P1; CHILD; CHILD, PRESCHOOL; CHROMOSOME BREAKAGE; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 11; DNA TOPOISOMERASES, TYPE II; FEMALE; GENOMIC LIBRARY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; KARYOTYPING; LEUKEMIA, LYMPHOCYTIC, ACUTE; LEUKEMIA, MYELOCYTIC, ACUTE; LYMPHOMA, NON-HODGKIN; MALE; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES; NEOPLASMS, SECOND PRIMARY;

EID: 0030976312     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199707)19:3<150::AID-GCC3>3.0.CO;2-X     Document Type: Article

References (26)

1. Akao Y, Seto M, Takahashi T, Kubonishi I, Miyoshi I, Nakazawa S, Tsujimoto Y, Croce CM, Ueda R (1991) Molecular cloning of the chromosomal breakpoint of a B-cell lymphoma With the t(11;14)(q23;q32) translocation. Cancer Res 51:1574-1576.
2. Arai Y, Hosoda F, Nakayama K, Ohki M (1996) A yeast artificial chromosome contig and Not I restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3. Genomics 35:196-206.
3. Bohlander SK, Espinosa R III, Fernald AA, Rowley JD, Le Beau MM, Diaz MO (1994) Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization. Cytogenet Cell Genet 65:108-110.
4. Chen Z, Brand NJ, Chen A, Chen S, Tong J-H, Wang Z-Y, Waxman S, Zelent A (1993) Fusion between a novel Krüppel like zinc finger gene and the retinoic acid receptor: A locus due to a variant t(11;17) translocation associated with acute promyrlovyyiv leukemia, EMBO J 12:1161-1167.
5. Chumakov IM, LeGall I, Billault A, Ougen P, Soularue P, Guillou S, Rigault P, Bui H, DeTand MF, Barillot E, Cohen D (1992) Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library. Nat Genet 1:222-225.
6. Gibbons B, Czepulkowski B, Tucker J, Simpson E, Amess JAL, Young BD, Lister TA (1987) Subtle abnormalities in the short arm of chromosome 11 in acute mycloid leukemia. Cancer Genet Cytogenet 28:287-297.
7. Gill Super HJ, McCabe NR, Thirman MJ, Larson LA, Le Beau MM, Pederson-Bjergaad J, Philip P, Diaz MO, Rowley JD (1993) Rearrangements of MLL gene in therapy-related acute leukemia in patients previously treated with agents targeting DNA-topoisomerase II. Blond 82:3705-3711.
8. Gu Y, Nakamura T, Alder H, Prasad R, Canaani O, Cimino G, Crocc CM, Canaani F, (1992) The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophilia trithorax, to the AF-4 gene. Cell 71:701-708.
9. Ichikawa H, Shimizu K, Saito A, Wang D, Oliva R, Kobayashi H, Kaneko Y, Miyoshi H, Smith CL, Cantor CR, Ohki M (1992) Long-distance restriction mapping of the proximal long arm of human chromosome 21 with NotI linking clones. Proc Natl Acad Sci USA 89:23-27.
10. Inaba T, Hayashi Y, Hanada R, Nakashima M, Yamamoto K, Nishida T (1988) Childhood myclodysplastic syndromes with 11p15 translocation. Cancer Genet Cytogenet 34:41-46.
11. ISCN (1995) Recommendations ot the international Standing Committee on Human Cytogenetic Nomenclature. Mitelman F (ed). Basel: S. Karger.
12. Kobayashi H, Espinosa R III, Thirman MJ, Gill HJ, Fernald AA, Diaz MO, Le Beau MM, Rowley JD (1993a) Heterogencity of breakpoints of 11q23 rearrangements in hematologic malignancies idetified with fluorescence in sity hybridization. Blood 82:547-551.
13. Kobayashi H, Espinosa R III, Thirman MJ, Davis E, Diaz MO, Le Bean MM, Rowley JD (1993b) Variability of 11q23 rearrangements in hematopoietic cell lines identified with fluorescence in situ hybridization. Blood 81:3027-3033.
14. Kobayashi H, Maseki N, Homma C, Sakurai M, Kaneko Y (1994) Clinical significance of chromosomal abnormalities in childhood acute lymphoblastic leukemia in Japan. Leukemia 8: 1944-1950.
15. MeCabe NR, Burnett RC, Gill HJ, Thirman MJ, Mbankollo D, Kipiniak M, Van Melle E, Ziemin-Van der Poel S, Rowley JD, Diaz MO (1992) Cloning of DNAs of the MLL gene that detect DNA rearrangements and altered RNA transcripts in human leukemic cells with 11q23 translocations. Proc Natl Acad Sci USA 89:11794-11798.
16. Meerabux J, Vaspo M-L, Roebrock AJ, Van de Ven WJM, Lister TA, Young BD (1996) A new member of the proprotein convertase gene family (LPG) is located at a chromosome translocation breakpoint in lymphoma. Cancer Res 56:448-451.
17. Mitelman F (1994) Catalog of Chromosome Aberrations in Cancer. New York: Wiley-Liss.
18. Ohira M, Ichikawa H, Suzuki E, Iwai M, Suzuki K, Saito-Ohara F, Ikeuchi T, Chumakov IM, Tanahashi H, Tashiro K, Sakaki Y, Ohki M (1996) A 1.6-Mb P1-based physical map of the Down syndrome region on chromosome 21. Genomics 33:65-74.
19. Pederson-Bjergaard J, Rowley JD (1994) The balanced and unbalanced chromosome aberrations of acute myeloid leukemia mayn develop in different ways and may contribute differently to malignant transformation. Blood 83:2780-2786.
20. Pui C-H, Behm FG, Raimondi SC, Dodge RK, George SL, Rivera GK, Mirro J, Kalwinsky DK, Dahl GV, Murphy SB, Crist WM, Williams DL(1989) Secondary acute leukemia in children treated for acute lymphoid leukemia. N Engl J Med 321:136-142.
21. Stark B, Jeison M, Shohat M, Goshen Y, Vogel R, Cohen IJ, Yaniv I, Kapkubsjt C, Zaizov R (1994) Involvement of 11p15 and 3q21q26 in therapy-related myeloid leukemia (t-ML) in children. Cancer Genet Cytogenet 75:11-22.
22. Strissel-Broeker PLS, Gill Super H, Thirman MJ, Pomykala H, Yonebayashi Y, Tanabe S, Zeleznik-Le N, Rowley JD (1996) Distribution of 11q23 breakpoints within the MLL breakpoint cluster region in de novo acute leukemia and in treatment-related acute myeloid leukemia: Correlation with scaffold attachment regions and topoisomerase II consensus binding sites. Blood 87:1912-1922.
23. Tanigami A, Tokino T, Takiguchi S, Mori M, Glaser T, Park JW, Jones C, Nakamura Y (1992) Mapping of 262 DNZ markers into 24 intervals on human chromosome 11. Am J Hum Genet 50:56-64.
24. Thirman MJ, Gill HJ, Burnett RC, Mbangkollo D, McCabe NR, Kobayashi H, Zicmin-van der Poel S, Kaneki Y, Morgan R, Sandberg AA, Chaganti RSK, Larson RA, Le Beau MM, Diza MO, Rowley JD (1993) Rearrangement of the MLL gene in acute lymphoblastic and acute mycloid leukemias with 11q23 chromosomal translocations. N Engl J Med 329:909-914.
25. Tkachuck DC, Kohler S, Cleary, ML, (1992) Involvement of a homolog of Drosophilia trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 71:691-700.
26. Yamamoto K, Seto M, Akao Y, Iida S, Nakazawa S, Oshimura M, Takahashi T, Ueda R (1993) Gene rearrangement and truncated mRNA in cell lines with 11q23 translocations. Oncogene 8:479-485.