Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2)

Cancer Genetics and Cytogenetics

Volumn 179, Issue 1, 2007, Pages 85-87

  Takeuchi, Mai ^a   Katayama, Yoshio ^a   Okamura, Atsuo ^a   Yamamoto, Katsuya ^a   Shimoyama, Manabu ^a   Matsui, Toshimitsu ^a  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BCR ABL GENE; CASE REPORT; CHROMOSOME TRANSLOCATION; CHRONIC MYELOID LEUKEMIA; FEMALE; FUSION GENE; GENETIC VARIABILITY; HUMAN; IRON DEFICIENCY ANEMIA; LETTER; LEUKOCYTOSIS; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ADULT; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FUSION PROTEINS, BCR-ABL; GENES, ABL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOGENOUS, CHRONIC, BCR-ABL POSITIVE; PHILADELPHIA CHROMOSOME; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TRANSLOCATION, GENETIC;

EID: 35549005289     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2007.08.010     Document Type: Letter

References (12)

1. El-Zimaity M.M., Kantarjian H., Talpaz M., O'Brien S., Giles F., Garcia-Manero G., Verstovsek S., Thomas D., Ferrajoli A., Hayes K., Nebiyou Bekele B., Zhou X., Rios M.B., Glassman A.B., and Cortes J.E. Results of imatinib mesylate therapy in chronic myelogenous leukaemia with variant Philadelphia chromosome. Br J Haematol 125 (2004) 187-195
2. Emig M., Saussele S., Wittor H., Weisser A., Reiter A., Willer A., Berger U., Hehlmann R., Cross N.C., and Hochhaus A. Accurate and rapid analysis of residual disease in patients with CML using specific fluorescent hybridization probes for real time quantitative RT-PCR. Leukemia 13 (1999) 1825-1832
3. Bartram C.R., Anger B., Carbonell F., and Kleihauer E. Involvement of chromosome 9 in variant Ph1 translocation. Leuk Res 9 (1985) 1133-1137
4. Guillaume B., Ameye G., Libouton J.M., Dierlamm J., Vaerman J.L., Straetmans N., Ferrant A., Verellen-Dumoulin C., and Michaux L. Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;22;21)(q34;q11;q22). Cancer Genet Cytogenet 116 (2000) 166-169
5. Mancini M., Nanni M., Cedrone M., De Cuia M.R., Rondinelli M.B., Malagnino F., and Alimena G. Application of fluorescence in situ hybridization in defining a complex t(9;21;22) Ph formation. Haematologica 79 (1994) 536-539
6. Vallcorba I., Garcia-Sagredo J.M., San Roman C., Ferro M.T., Gonzalez A., Cabello P., and Villegas A. Translocation (9;22;21) in a chronic myeloid leukemia: fluorescence in situ hybridization definition. Cancer Genet Cytogenet 104 (1998) 72-73
7. Zhang J., Meltzer P., Jenkins R., Guan X.Y., and Trent J. Application of chromosome microdissection probes for elucidation of BCR-ABL fusion and variant Philadelphia chromosome translocations in chronic myelogenous leukemia. Blood 81 (1993) 3365-3371
8. Johansson B., Fioretos T., and Mitelman F. Cytogenetic and molecular genetic evolution of chronic myeloid leukemia. Acta Haematol 107 (2002) 76-94
9. Jeandidier E., Dastugue N., Mugneret F., Lafage-Pochitaloff M., Mozziconacci M.J., Herens C., Michaux L., Verellen-Dumoulin C., Talmant P., Cornillet-Lefebvre P., Luquet I., Charrin C., Barin C., Collonge-Rame M.A., Pérot C., Van den Akker J., Grégoire M.J., Jonveaux P., Baranger L., Eclache-Saudreau V., Pagès M.P., Cabrol C., Terré C., Berger R., and Groupe Français de Cytogénétique Hématologique (GFCH). Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique. Cancer Genet Cytogenet 166 (2006) 1-11
10. dos Santos Aguiar S., de Jesus Girotto Zambaldi L., dos Santos A.M., Pinto Jr. W., and Brandalise S.R. Comparative genomic hybridization analysis of abnormalities in chromosome 21 in childhood osteosarcoma. Cancer Genet Cytogenet 175 (2007) 35-40
11. Shen J.J., Williams B.J., Zipursky A., Doyle J., Sherman S.L., Jacobs P.A., Shugar A.L., Soukup S.W., and Hassold T.J. Cytogenetic and molecular studies of Down syndrome individuals with leukemia. Am J Hum Genet 56 (1995) 915-925
12. Bera T.K., Zimonjic D.B., Popescu N.C., Sathyanarayana B.K., Kumar V., Lee B., and Pastan I. POTE, a highly homologous gene family located on numerous chromosomes and expressed in prostate, ovary, testis, placenta, and prostate cancer. Proc Natl Acad Sci U S A 99 (2002) 16975-16980 [Erratum in: Proc Natl Acad Sci U S A 2003;100:1462]