Expression of genes encoding centrosomal proteins and the humoral response against these proteins in chronic myeloid leukemia

被引:5
|
作者
Smahelova, Jana [1 ]
Kastankova, Iva [1 ]
Polakova, Katerina Machova [2 ]
Klamova, Hana [3 ]
Zemanova, Karla [2 ]
Tachezy, Ruth [1 ]
Hamsikova, Eva [1 ]
Smahel, Michal [1 ,4 ]
机构
[1] Inst Hematol & Blood Transfus, Dept Immunol, CZ-12820 Prague, Czech Republic
[2] Inst Hematol & Blood Transfus, Dept Mol Genet, CZ-12820 Prague, Czech Republic
[3] Inst Hematol & Blood Transfus, Clin Dept, CZ-12820 Prague, Czech Republic
[4] Charles Univ Prague, Dept Genet & Microbiol, Fac Sci, BIOCEV, Prumyslova 595, CZ-25242 Vestec, Czech Republic
关键词
centrosome; chronic myeloid leukemia; expression; antibody; BCR-ABL1; imatinib mesylate; CHRONIC LYMPHOCYTIC-LEUKEMIA; T-CELL RESPONSES; TARGET; IMMUNOTHERAPY; IMATINIB; DISEASE; KINASE; CML; OVEREXPRESSION; MANAGEMENT;
D O I
10.3892/or.2016.5226
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As the extent of centrosome abnormalities in chronic myeloid leukemia (CML) correlates with disease stage and karyotype alterations, abnormal expression of genes encoding centrosomal proteins may be an early prognostic marker of disease progression. In the present study, we showed that in comparison with healthy controls, the expression of four centrosomal genes (AURKA, HMMR, PLK1 and ESPL1) in the peripheral blood of CML patients was significantly enhanced at diagnosis and decreased to the basal level in most patients treated with imatinib mesylate for three months. In the remaining patients (17%), this decrease was delayed and was associated with worse overall survival. The detection of antibodies in sera showed that patients with higher overall antibody production had superior outcomes in terms of achieving major molecular response and failure-free survival. These data suggest that the dynamics of the response of centrosomal genes should be considered as a risk factor and immunity against centrosomal proteins may contribute to treatment response.
引用
收藏
页码:547 / 554
页数:8
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