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DOI 10.1093/jjco/hyv064

Медицинская библиотека · Japanese journal of clinical oncology · 2015

Correlation of C/EBPα expression with response and resistance to imatinib in chronic myeloid leukaemia.

Kagita Sailaja, Uppalapati Srihari, Gundeti Sadasivudu, Digumarti Raghunadharao

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

Altered differentiation is a common feature of haematopoietic malignancies with poor prognosis. CAAT/enhancer binding protein alpha (C/EBPα) is a key transcription factor that regulates myeloid differentiation. This study is aimed to know the prognostic value of CAAT/enhancer binding protein alpha expression and correlate its expression with response to imatinib therapy.

METHODS

We quantified the expression of C/EBPα gene in 126 chronic myeloid leukaemia samples (82 from newly diagnosed and 44 from imatinib-resistant patients) and 20 control samples. C/EBPα mRNA level was measured by real-time quantitative polymerase chain reaction using the ΔΔCT method.

RESULTS

C/EBPα expression level was significantly lower in the imatinib-resistant group than in the pretreatment and control group (P = 0.0398). Low CAAT/enhancer binding protein alpha levels in the imatinib-resistant group were significantly associated with advanced phase (P = 0.04), with more peripheral blasts (P = 0.0001), high BCR-ABL levels (P = 0.018) and T315I and P-loop mutations (P = 0.0002). In the pretreatment group, low expression showed association with high EUTOS risk score (P = 0.03) and possible partial cytogenetic response (P = 0.010).

CONCLUSIONS

Our results suggest that low expression of CAAT/enhancer binding protein alpha might have a role in the response to imatinib and progression of disease in patients with chronic myeloid leukaemia.

Для цитирования: Kagita Sailaja, Uppalapati Srihari, Gundeti Sadasivudu, Digumarti Raghunadharao. Correlation of C/EBPα expression with response and resistance to imatinib in chronic myeloid leukaemia.. Japanese journal of clinical oncology. 2015. DOI: 10.1093/jjco/hyv064.

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