High expression of AURKA and AURKB is associated with unfavorable cytogenetic abnormalities and high white blood cell count in patients with acute myeloid leukemia

被引:54
作者
Lucena-Araujo, Antonio R. [1 ]
de Oliveira, Fabio Morato [1 ]
Leite-Cueva, Sabrina Dias [2 ]
dos Santos, Guilherme Augusto [1 ]
Falcao, Roberto Passeto [1 ]
Rego, Eduardo Magalhaes [1 ]
机构
[1] Univ Sao Paulo, Med Sch Ribeirao Preto, Natl Inst Sci & Technol Cell Based Therapy, Div Hematol,Dept Internal Med, BR-14048900 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Med Sch Ribeirao Preto, Natl Inst Sci & Technol Cell Based Therapy, Dept Genet, BR-14048900 Ribeirao Preto, Brazil
基金
巴西圣保罗研究基金会;
关键词
Acute myeloid leukemia; Aurora kinase; Cytogenetics; AURORA KINASE INHIBITORS; CHROMOSOMAL INSTABILITY; A EXPRESSION; CARCINOMA; MUTATIONS;
D O I
10.1016/j.leukres.2010.07.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the present study, we analyzed AURKA and AURKB gene expression in 70 acute myeloid leukemia (AML) patients. There was no difference between leukemic samples and bone marrow mononuclear cells (BMMCs, n = 8) or CD34(+) progenitors (n = 10) from healthy donors. High white blood cells (WBC) counts were observed in the AURKA(+) and AURKB(+) groups, but no significant differences regarding age, gender, platelet counts or frequency of FLT3-ITD mutations. AURKA, but not AURKB, expression was independently associated with high WBC counts (OR: 3.15, 95% CI 1.07-9.24, p = 0.03). Moreover, the majority of cases that overexpressed AURKA and AURKB presented unfavorable cytogenetic abnormalities (p < 0.001). In conclusion, we described a significant association between overexpression of AURKA/B and cytogenetics findings in AML, which may be relevant to new therapeutic approaches, based on Aurora kinase inhibitors. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:260 / 264
页数:5
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