Characterization of hsa_circ_0004277 as a new biomarker for acute myeloid leukemia via circular RNA profile and bioinformatics analysis

W Li, C Zhong, J Jiao, P Li, B Cui, C Ji… - International journal of …, 2017 - mdpi.com
W Li, C Zhong, J Jiao, P Li, B Cui, C Ji, D Ma
International journal of molecular sciences, 2017mdpi.com
Circular RNAs (circRNAs) represent a widespread class of non-coding RNAs, which drew
little attention in the past. Recently, limited data showed their promising future to act as
biomarkers in human cancer, but the characteristics and functions remain largely unknown
in hematopoietic malignancies, especially in leukemia. In this study, with the help of circRNA
microarray, we demonstrated the expression profile of circRNAs in acute myeloid leukemia
(AML) patients, and identified a large number of circRNAs possibly expressed in a leukemia …
Circular RNAs (circRNAs) represent a widespread class of non-coding RNAs, which drew little attention in the past. Recently, limited data showed their promising future to act as biomarkers in human cancer, but the characteristics and functions remain largely unknown in hematopoietic malignancies, especially in leukemia. In this study, with the help of circRNA microarray, we demonstrated the expression profile of circRNAs in acute myeloid leukemia (AML) patients, and identified a large number of circRNAs possibly expressed in a leukemia specific manner. We also described a circRNA signature related to AML risk-status based on the bioinformatics prediction. In particular, a downregulated circRNA, hsa_circ_0004277, was characterized and functionally evaluated in a cohort of 115 human samples, thus offering a potential diagnostic marker and treatment target in AML. Interestingly, we found chemotherapy could significantly restore the expression of hsa_circ_0004277, indicating the increasing level of hsa_circ_0004277 was associated with successful treatment. Furthermore, a detailed circRNA–miRNA–mRNA interaction network was presented for hsa_circ_0004277, allowing us to better understand its underlying mechanisms for function in AML.
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