Expression of genes encoding centrosomal proteins and the humoral response against these proteins in chronic myeloid leukemia
Language English Country Greece Media print-electronic
Document type Journal Article
PubMed
27840977
DOI
10.3892/or.2016.5226
Knihovny.cz E-resources
- MeSH
- Centrosome immunology metabolism MeSH
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive genetics immunology MeSH
- Adult MeSH
- Immunity, Humoral * genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Neoplasm Proteins genetics immunology MeSH
- Cell Cycle Proteins genetics immunology MeSH
- Gene Expression Regulation, Leukemic MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Neoplasm Proteins MeSH
- Cell Cycle Proteins MeSH
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.
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