Identification of pericentric inversion 12, inv(12)(p13.1q11), by Fluorescence in situ hybridization in a patient with acute myeloid leukemia (AML-M6)

Cancer Genetics and Cytogenetics

Volumn 97, Issue 2, 1997, Pages 157-160

  Sato, Yuko ^a,b   Bohlander, Stefan K ^a,c   Kobayashi, Hirofumi ^a,d   Suto, Yoshimasa ^a,e   Davis, Elizabeth M ^a   Espinosa III, Rafael ^a   Le Beau, Michelle M ^a   Rowley, Janet D ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b NATIONAL CENTER FOR GLOBAL HEALTH AND MEDICINE   (Japan)

^c UNIVERSITY OF GÖTTINGEN   (Germany)

^d SAITAMA CANCER CENTER   (Japan)

^e HIROSAKI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CHROMOSOME 12; CHROMOSOME INVERSION; COSMID; CYTOGENETICS; DNA NICK TRANSLATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HUMAN; METAPHASE; PRIORITY JOURNAL;

CHROMOSOME BANDING; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; DNA PROBES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; KARYOTYPING; LEUKEMIA, ERYTHROBLASTIC, ACUTE; MIDDLE AGED;

EID: 0030752429     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00335-4     Document Type: Article

References (19)

1. Kobayashi H, Rowley JD (1995): Identification of undetected 12p13 translocations and associated deletions with fluorescence in situ hybridization. Genes Chromosom Cancer 12:66-69.
2. Olopade Ol, Thangavelu M, Larson RA, Mick R, Kowal-Vern A, Schumacher HR, Le Beau MM, Vardiman JW, Rowley JD (1992): Clinical, morphologic, and cytogenetic characteristics of 26 patients with acute erythroblastic leukemia. Blood 80:2873-2882.
3. Le Beau MM (1991): Cytogenetic analysis of hematological malignant disease. In: The ACT, Cytogenetics Laboratory Manual. M J Barch, ed. Raven Press Ltd., New York, pp 395-445.
4. ISCN (1995): An International System for Human Cytogenetic Nomenclature (1995). F Mitelman, ed. S. Karger, Basel, Switzerland.
5. Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley ID (1994): Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases. Blood 84:3473-3482.
6. KIP1 gene to 12p13 and its analysis in leukemias. Cancer Res 55:1206-1210.
7. Rowley JD, Diáz MO, Espinosa R, Patel YD, van Melle E, Ziemin S, Taillon-Miller P, Lichter P, Evans GA, Kersey JH, Ward DC, Domer PH, Le Beau MM (1990): Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: Identification of 11q23 translocation breakpoints with a yeast artificial chromosome. Proc Natl Acad Sci USA 97:8358-9372.
8. Bohlander SK, Espinosa R, Fernald AA, Rowley JD, Le Beau MM, Diáz, MO (1994): Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization. Cytogenet Cell Genetics 65:108-110.
9. Mitelman F (1994): Catalog of Chromosome Aberrations, 5th ed. Wiley-Liss, New York.
10. Golub TR, Barker GF, Lovett M, Gilliland DG (1994): Fusion of PDGF receptor β to a novel ETS-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77:307-316.
11. Golub TR, Barker GF, Bohlander SK, Hiebert SW, Ward DC, Bray-Ward P, Morgan E, Raimondi SC, Rowley JD, Gilliland DG (1995): Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc Natl Acad Sci USA 92:4917-4921.
12. Romana SP, Mauchauffe M, Le Coniat M, Chumakov I, Le Paslier D, Berger R, Bernard OA (1995): The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood 85:3662-3670.
13. Papadopoulos P, Ridge SA, Boucher CA, Stocking C, Wiedemann LM (1995): The novel activation of ABL by fusion to an ets-related gene, TEL Cancer Res 55:34-38.
14. Golub TR, Goga A, Barker GF, Afar DE, McLaughlin AJ, Bohlander SK, Rawley JD, Witte ON, Gilliland DG (1996): Oligomerization of the ABL tyrosine kinase by the ETS protein TEL in human leukemia. Mol Cell Biol 16:4107-4116.
15. Buijs A, Sherr S, van Baal S, van Bezouw S, van der Plas D, Geurts van Kessel A, Riegman P, Lekanne Deprez R, Zwarthoff E, Hagemeijer A, Grosveld G (1995): Translocation (12;22)(p13pq11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11. Oncogene 10:1511-1519.
16. Rebeiro RC, Abromowitch M, Raimondi SC, Murphy SB, Behm F, Williams DL (1987): Clinical and biologic hallmarks of the Philadelphia chromosome in childhood acute lymphoblastic leukemia. Blood 70:948-953.
17. Nowell PC, Vonderheid EC, Besa E, Hoxie JA, Moreau L, Finan JB (1986): The most common chromosome change in 86 chronic B or T cell tumors: A 14q32 translocation. Cancer Genet Cytogenet 19:329-227.
18. Mitelman F, Manolova Y, Manolov G, Billstrom R, Heim S, Kristoffersson U, Mandahl N (1986): High resolution analysis of the 5q- marker chromosome in refractory anemia. Hereditas 105:49-54.
19. Raimondi SC, Behm FG, Robertson PK, Pui C-H, Rivera GK, Murphy SB, Williams DL (1988): Cytogenetics of childhood T-cell leukemia. Blood 72:1560- 1566.