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High miR-24 expression is associated with risk of relapse and poor survival in acute leukemia. | LitMetric

AI Article Synopsis

  • MicroRNAs (miRNAs), specifically miR-24, are shown to be crucial in the development and progression of acute leukemia (AL), with miR-24 linked to the survival of hematopoietic cells.
  • A study measuring miR-24 expression in 147 AL patients versus 100 healthy individuals found significantly higher levels of miR-24 in AL patients, especially in those with acute myeloid leukemia (AML).
  • High levels of miR-24 were associated with shorter overall survival in AL patients and identified as an independent prognostic marker, suggesting its potential role in predicting clinical outcomes for these patients.

Article Abstract

MicroRNAs (miRNAs) play an essential role in the development and progression of acute leukemia (AL). miR-24 promotes the survival of hematopoietic cells. However, little is known concerning the function of miR-24 in human AL. The aim of the present study was to investigate the clinical significance of miR-24 expression in AL. miR-24 expression in 147 patients with AL and 100 healthy individuals was measured by quantitative reverse transcriptase-polymerase chain reaction (RT-qPCR). The results showed that compared with the healthy individuals, the expression of miR-24 in AL patients was significantly higher (p<0.001). In addition, miR-24 was expressed at significantly higher levels in acute myeloid leukemia (AML) patients and at significantly lower levels in acute lymphoblastic leukemia (ALL) (p<0.001). More importantly, Kaplan-Meier analysis showed that AL patients with high miR-24 expression tended to have shorter overall survival (p<0.05). In the multivariate analysis stratified for known prognostic variables, miR-24 was identified as an independent prognostic marker. Our data indicated that miR-24 upregulation was associated with poor prognosis in AL. miR-24 was identified for the first time as an independent marker for predicting the clinical outcome of AL patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358084PMC
http://dx.doi.org/10.3892/or.2015.3787DOI Listing

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