Dysregulation of miR-124-1 predicts favorable prognosis in acute myeloid leukemia

Clin Biochem. 2014 Jan;47(1-2):63-6. doi: 10.1016/j.clinbiochem.2013.09.020. Epub 2013 Oct 14.

Abstract

Objective: MicroRNA miR-124 has been suggested as a tumor suppressor for its role in inhibiting cell growth, inducing differentiation and promoting apoptosis. The present study was aimed to investigate the expression status of miR-124-1 and its clinical relevance in patients with acute myeloid leukemia (AML).

Designs and methods: Real-time quantitative PCR was performed to detect the expression level of miR-124-1 in AML patients. The clinical significance of miR-124-1 expression in AML was investigated.

Results: miR-124-1 underexpression was identified in 30 (36%) of 83 AML patients. No significant difference could be observed in sex, age and blood parameters between the patients with and without miR-124-1 underexpression. The frequency of miR-124-1 underexpression was higher in the patients with t(15;17) than in others (62% versus 30%, P = 0.040). The status of miR-124-1 expression was not correlated with the mutations of nine genes (FLT3-ITD, NPM1, C-KIT, IDH1/IDH2, DNMT3A, N/K-RAS and C/EBPA). The patients with miR-124-1 underexpression had borderline longer overall survival and relapse-free survival than those without miR-124-1 underexpression (P = 0.052 and 0.045, respectively).

Conclusions: These findings suggest that miR-124-1 underexpression is a common event and might have a favorable impact on prognosis in AML.

Keywords: Acute myeloid leukemia; miR-124; microRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Case-Control Studies
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / pathology*
  • Male
  • MicroRNAs / genetics*
  • Middle Aged
  • Nucleophosmin
  • Prognosis
  • Real-Time Polymerase Chain Reaction
  • Young Adult

Substances

  • MIRN124 microRNA, human
  • MicroRNAs
  • NPM1 protein, human
  • Nucleophosmin