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Expression of microRNA-181 determines response to treatment with azacitidine and predicts survival in elderly patients with acute myeloid leukaemia
- Source :
- Oncology Letters
- Publication Year :
- 2016
- Publisher :
- D.A. Spandidos, 2016.
-
Abstract
- MicroRNAs (miRs) are small non-coding RNAs that play important roles in cell differentiation and survival. Abnormal expression of miRs has been demonstrated in numerous types of cancer, including acute myeloid leukaemia (AML). The aim of the present study was to evaluate miR-181 expression at diagnosis and following the completion of chemotherapy in AML patients, with regard to clinical response and outcome, particularly in patients treated with azacitidine. miR-181 expression was analysed using reverse transcription-quantitative polymerase chain reaction in 95 bone marrow specimens from newly diagnosed AML patients and in 20 healthy subjects for comparison. The results revealed upregulated miR-181 expression in the total cohort of AML patients, which was correlated with longer survival. However, in a subset of older AML patients treated with azacitidine, low miR-181 expression at diagnosis was a predictor for complete remission and prolonged survival. The findings indicated that miR-181 has an important role in AML and determines response to azacitidine treatment in older AML patients.
- Subjects :
- 0301 basic medicine
Cancer Research
azacitidine
medicine.medical_treatment
Azacitidine
Biology
acute myeloid leukemia
survival
03 medical and health sciences
0302 clinical medicine
remission
hemic and lymphatic diseases
microRNA
expression
medicine
Chemotherapy
response
Oncogene
Cancer
Articles
medicine.disease
Molecular medicine
030104 developmental biology
medicine.anatomical_structure
Oncology
miR-181
030220 oncology & carcinogenesis
Cohort
Cancer research
Bone marrow
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 17921082 and 17921074
- Volume :
- 12
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Oncology Letters
- Accession number :
- edsair.doi.dedup.....cbdcb5226496f1a61be5877970525637