Down-Regulation of miR-186 Correlates with Poor Survival in de novo Acute Myeloid Leukemia

Clin Lab. 2016;62(1-2):113-20. doi: 10.7754/clin.lab.2015.150606.

Abstract

Background: MicroRNA-186 (miR-186) plays an important role in the pathogenesis of several cancers. Our study was intended to investigate the expression status and the prognostic implication of miR-186 in acute myeloid leukemia (AML).

Methods: Real-time quantitative PCR was carried out in 112 de novo AML patients and 28 controls.

Results: The level of miR-186 expression in AML was significantly down-regulated compared to normal controls (p < 0.001). Patients with low miR-186 expression presented significantly older age than those with high miR-186 expression (p = 0.004). MiR-186high patients had a significantly higher frequency of CEBPA mutation than miR-186low patients (20% and 4%, respectively, p = 0.022). In addition, miR-186low patients had a significantly lower complete remission (CR) rate (30% vs. 53%, respectively, p = 0.028) than miR-186high patients. Moreover, miR-186low patients showed significantly shorter overall survival (OS) time than miR-186high patients in both whole AML and non-M3 patients (p = 0.023 and 0.026, respectively). Additionally, the adverse prognostic impact of miR-186 down-regulation was also shown in both whole AML and non-M3 patients without CEBPA mutation (p = 0.017 and 0.023, respectively).

Conclusions: Our study suggests that miR-186 down-regulation is a frequent event and predicts poor prognosis in de novo AML patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / genetics
  • CCAAT-Enhancer-Binding Proteins / genetics
  • Case-Control Studies
  • DNA Mutational Analysis
  • Down-Regulation
  • Female
  • Gene Expression Regulation, Leukemic
  • Humans
  • Kaplan-Meier Estimate
  • Leukemia, Myeloid, Acute / genetics*
  • Leukemia, Myeloid, Acute / mortality
  • Leukemia, Myeloid, Acute / therapy
  • Male
  • MicroRNAs / genetics*
  • Middle Aged
  • Mutation
  • Predictive Value of Tests
  • Real-Time Polymerase Chain Reaction
  • Remission Induction
  • Risk Factors
  • Time Factors
  • Treatment Outcome
  • Young Adult

Substances

  • Biomarkers, Tumor
  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, human
  • MIRN186 microRNA, human
  • MicroRNAs