Olea europaea leaf extract alters microRNA expression in human glioblastoma cells

Berrin Tunca1, Gulcin Tezcan, Gulsah Cecener

  • 1Department of Medical Biology, Medical Faculty, Uludag University, Bursa, Turkey. btunca@uludag.edu.tr

Abstract

Insights

Olea europaea leaf extract (OLE) shows anticancer effects against glioblastoma multiforme (GBM) by altering microRNA (miRNA) expression. This extract, when combined with temozolomide (TMZ), modulates key miRNAs involved in cell death pathways.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Glioblastoma multiforme (GBM) is a lethal primary brain tumor with limited therapeutic options.
  • Phytochemicals are being explored for their potential to induce tumor cell death.
  • MicroRNAs (miRNAs) play crucial roles in posttranscriptional gene regulation and are implicated in cancer.

Purpose of the Study:

  • To investigate the anticancer effects of Olea europaea leaf extract (OLE) on GBM.
  • To determine if OLE modulates miRNA expression in GBM cells.
  • To assess the combined effect of OLE and temozolomide (TMZ) on GBM.

Main Methods:

  • Anti-proliferative activity of OLE was assessed in human glioblastoma T98G cells using trypan blue and WST-1 assays.
  • miRNA expression profiling was performed using PCR array analysis after treatment with OLE and TMZ.
  • Bioinformatic analysis was conducted to identify potential mRNA targets of modulated miRNAs.

Main Results:

  • OLE demonstrated significant anti-proliferative effects on T98G glioblastoma cells.
  • Treatment with both OLE and TMZ led to significant upregulation of specific miRNAs, including miR-181b, miR-153, miR-145, miR-137, and let-7d.
  • Identified miRNA target genes are involved in crucial cellular processes such as the cell cycle and apoptosis.

Conclusions:

  • OLE exhibits anticancer properties in GBM by modulating miRNA expression.
  • The findings suggest a potential synergistic effect between OLE and TMZ in altering miRNA profiles.
  • OLE warrants further investigation for its potential as an adjuvant therapy in GBM treatment.