Screening for EVI1: ectopic expression absent in T-cell acute lymphoblastic leukemia patients and cell lines

Cancer Genetics and Cytogenetics

Volumn 171, Issue 1, 2006, Pages 79-80

  De Weer, A ^a   Poppe, B ^a   Cauwelier, B ^a   Van Roy, N ^a   Dastugue, N ^b   Hagemeijer, A ^c   De Paepe, A ^a   Speleman, F ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b CHU PURPAN   (France)

^c UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; BLOOD CELL COUNT; CANCER SURVIVAL; CELL LINE; CHROMOSOME INVERSION; CHROMOSOME TRANSLOCATION; ECOTROPIC VIRAL INTEGRATION SITE 1 GENE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; HUMAN; KARYOTYPE; LETTER; ONCOGENE; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; SURVIVAL RATE; SURVIVAL TIME; T CELL LEUKEMIA; VIRUS EXPRESSION;

CELL LINE, TUMOR; DNA-BINDING PROTEINS; GENE EXPRESSION REGULATION, NEOPLASTIC; HUMANS; LEUKEMIA, T-CELL, ACUTE; PROTO-ONCOGENES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TRANSCRIPTION FACTORS;

EID: 33751014063     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2006.07.004     Document Type: Letter

References (5)

1. Grabher C., von Boehmer H., and Look A.T. Notch activation in the molecular pathogenesis of T-cell acute lymphoblastic leukaemia. Nat Rev Cancer 6 (2006) 347-359
2. Fröhling S., Scholl C., Gilliland D.G., and Levine R.L. Genetics of myeloid malignancies: pathogenetic and clinical implications. J Clin Oncol 23 (2005) 6285-6295
3. Buonamici S., Li D., Chi Y., Zhao R., Wang X., Brace L., Ni H., Saunthararajah Y., and Nucifora G. EVI1 induces myelodysplastic syndrome in mice. J Clin Invest 114 (2004) 713-719
4. Nucifora G. The EVI1 gene in myeloid leukemia. Leukemia 11 (1997) 2022-2031
5. Poppe B., Dastugue N., Vandesompele J., Cauwelier B., De Smet B., Yigit N., De Paepe A., Cervera J., Recher C., De Mas V., Hagemeijer A., and Speleman F. EVI1 is consistently expressed as principal transcript in common and rare recurrent 3q26 rearrangements. Genes Chromosomes Cancer 45 (2006) 439-456