Upregulation of microRNA-597 in myelodysplastic syndromes induces apoptosis through FOSL2 inhibition

Eur J Haematol. 2022 Dec;109(6):680-685. doi: 10.1111/ejh.13852. Epub 2022 Sep 7.

Abstract

Introduction: Dysregulation of microRNAs (miRNAs) has been associated with the pathophysiology of myelodysplastic syndrome (MDS). Trisomy 8 is the most frequent chromosomal abnormalities in Korean patients with MDS. We investigated the dysregulation of miR-597-5p, located on chromosome 8, which is reported to induce cell death in numerous cancers.

Materials and methods: We compared the expression profiles of miR-597-5p among 65 MDS patients and 11 controls, and analyzed the in vitro effects of miR-597 on leukemic cells using an acute myeloid leukemia cell line transfected with miR-597.

Results: We found that miR-597-5p levels were upregulated 4.05-fold in MDS patients compared to those in controls. In vitro study results demonstrated that transfection with a miR-597 mimic induced apoptosis through downregulation of FOS like 2 (FOSL2).

Conclusion: These findings suggest that upregulation of miR-597 induces apoptosis and that miR-597 has a possible role in the pathophysiology of MDS.

Keywords: MDS; apoptosis; dysregulation; microRNA; pathogenesis.

MeSH terms

  • Apoptosis
  • Fos-Related Antigen-2* / genetics
  • Fos-Related Antigen-2* / metabolism
  • Humans
  • Leukemia, Myeloid, Acute* / genetics
  • MicroRNAs* / genetics
  • Myelodysplastic Syndromes* / genetics
  • Myelodysplastic Syndromes* / metabolism
  • Transcription Factors / genetics
  • Up-Regulation

Substances

  • Fos-Related Antigen-2
  • FOSL2 protein, human
  • MicroRNAs
  • Transcription Factors
  • MIRN597 microRNA, human