Clinical Relevance of Differential RARα and PPARβ/δ Expression in Myelodysplastic Syndromes

In Vivo. 2024 Mar-Apr;38(2):657-664. doi: 10.21873/invivo.13486.

Abstract

Background/aim: Myelodysplastic syndromes (MDS) are clinically heterogeneous hematological malignancies with an increased risk of transformation to acute myeloid leukemia, emphasizing the importance of identifying new diagnostic and prognostic markers. This study sought to investigate the predictive ability of all-trans retinoic acid (ATRA)-dependent nuclear transcription factors RARα and PPARβ/δ gene expression in MDS patients.

Materials and methods: Peripheral blood specimens were collected from 49 MDS patients and 15 healthy volunteers. The specimens were further separated in Ficoll density gradient to obtain the mononuclear cells fractions. Gene expression analysis was carried out using quantitative real-time polymerase chain reaction (qRT-PCR) technique.

Results: In the mononuclear cell fractions of MDS patients, RARα expression was increased (p<0.05) and PPARβ/δ expression was decreased (p<0.01) compared to healthy volunteers. When RARα and PPARβ/δ expression was compared in groups of MDS patients with different risks of disease progression, no statistically significant difference was found for RARα expression, while PPARβ/δ expression was significantly lower in the high-risk group of patients compared to the low-risk group (p<0.05). The expression of RARα was significantly associated with overall survival (p<0.05). ROC analysis showed that the expression of PPARβ/δ, rather than RARα expression, could have potential diagnostic value for MDS patients (AUC=0.75, p=0.003 and AUC=0.65, p=0.081, respectively).

Conclusion: RARα and PPARβ/δ genes are putative biomarkers that may be associated with the diagnosis and prognosis of MDS.

Keywords: Myelodysplastic syndromes; PPARβ/δ; RARα; gene expression; prognostic significance.

MeSH terms

  • Clinical Relevance
  • Humans
  • Myelodysplastic Syndromes* / diagnosis
  • Myelodysplastic Syndromes* / genetics
  • PPAR delta* / genetics
  • PPAR delta* / metabolism
  • PPAR-beta* / genetics
  • PPAR-beta* / metabolism
  • Tretinoin

Substances

  • PPAR delta
  • PPAR-beta
  • Tretinoin
  • PPARD protein, human
  • RARA protein, human