Characterization of ABL1 expression in adult T-cell acute lymphoblastic leukemia by oligonucleotide array analysis

被引:10
作者
Chiaretti, Sabina
Tavolaro, Simona
Ghia, Emanuela Maria
Ariola, Cristina
Matteucci, Caterina
Elia, Loredana
Maggio, Roberta
Messina, Monica
Ricciardi, Maria Rosaria
Vitale, Antonella
Ritz, Jerome
Mecucci, Cristina
Guarini, Anna
Foa, Robin
机构
[1] Univ Roma La Sapienza, Div Hematol, Dept Cellular Biotechnol & Hematol, I-00161 Rome, Italy
[2] Univ Perugia, Policlin Monteluce, Hematol & Bone Marrow Transplantat Unit, I-06100 Perugia, Italy
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2007年 / 92卷 / 05期
关键词
NUP214/ABL1; T-lineage acute lymphoblastic leukemia; gene expression profile; ABL1; expression;
D O I
10.3324/haematol.10865
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives Recent data have highlighted an involvement of ABL1 in T-cell acute lymphoblastic leukemia (T-ALL). Specifically, the presence of a fusion gene involving ABL1 and NUP214, both located at 9q34, has been reported. We sought to evaluate whether TALL patients with overexpression of ABL showed a peculiar gene expression pattern and were characterized by having specific rearrangements. Design and Methods We previously assessed the expression profile of 128 adults with ALL by oligonucleotide arrays: 33 had T-ALL. In the current study, we evaluated the expression levels of ABL1 in T-ALL cases and found three patients who had ABL1 levels comparable to those detected in BCR/ABL(+) cases and one who had a significantly higher level of ABL1 expression. In order to establish the incidence of ABL1 overexpression in TALL, we evaluated 17 additional patients by quantitative (Q)-polymerase chain reaction (PCR) and reverse transcription (RT)-PCR. Results The three cases with ABL1 expression levels comparable to those found in BCR/ABL1 cases had a specific signature characterized by a high expression of genes involved in regulation of transcription. The fourth case, with the highest levels of ABL1, harbored the NUP214-ABL1 rearrangement, which was confirmed by fluorescence in situ hybridization (FISH). Three of the four patients were refractory to induction chemotherapy. Of the 17 additional patients evaluated by Q-PCR and RT-PCR, none showed ABL1 overexpression. Interpretation and Conclusions Overall, overexpression of ABL1 was found in 8% of T-ALL cases. These results underline the value of microarray analyses for the identification of specific signatures associated with ABL1 overexpression, as well as rearrangements, e.g. NUP214-ABL1, in adult T-ALL.
引用
收藏
页码:619 / 626
页数:8
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