CircRNA HLCS regulates lens epithelial cell apoptosis via miR-338-3p/BPNT1 axis

Int Ophthalmol. 2024 Mar 17;44(1):142. doi: 10.1007/s10792-024-03082-0.

Abstract

Purpose: The purpose of this study was to investigate the effect of circ_HLCS on age-related cataract (ARC).

Methods: Circ_HLCS, microRNA (miR)-338-3p, and bisphosphate 3'-nucleotidase 1 (BPNT1) were quantified by quantitative real-time polymerase chain reaction or western blot. Cell proliferation and cell viability were assessed by the 5-Ethynyl-2'-deoxyuridinr and cell counting kit-8 assays. Cell apoptosis was detected by flow cytometry. Targeted correlations among circ_HLCS, miR-338-3p, and BPNT1 were verified by the dual-luciferase reporter and RNA pull-down assays.

Results: circ_HLCS was diminished in ARC tissues and UV-treated SRA01/04 cells. Elevated content of circ_HLCS undermined UV-induced cell proliferation inhibition and apoptosis. Mechanistically, circ_HLCS directly targeted miR-338-3p, and circ_HLCS regulated BPNT1 expression through miR-338-3p. Furthermore, reduction of miR-338-3p ameliorated UV-induced SRA01/04 cell damage by increasing BPNT1 expression.

Conclusion: Taken together, these data suggested that circ_HLCS inhibited apoptosis of UV-treated SRA01/04 cells by miR-338-3p/BPNT1 axis. Therefore, circ_HLCS might be a potential therapeutic target for ARC.

Keywords: Age-related cataract; BPNT1; Circ_HLCS; miR-338-3p.

MeSH terms

  • Apoptosis
  • Cell Proliferation
  • Epithelial Cells
  • Humans
  • Lens, Crystalline*
  • MicroRNAs* / genetics
  • RNA, Circular / genetics

Substances

  • RNA, Circular
  • MicroRNAs
  • MIRN338 microRNA, human