6-Gingerol overcomes TMZ resistance in GBM by suppressing EMT and cell migration via the PI3K/Akt/β-catenin/c-Myc pathway

Int Immunopharmacol. 2025 Jun 26:159:114908. doi: 10.1016/j.intimp.2025.114908. Epub 2025 May 28.

Abstract

Glioblastoma multiforme (GBM) is the most aggressive and treatment-resistant primary brain tumor with acquired resistance to temozolomide (TMZ) posing a major clinical challenge. This study investigates the therapeutic potential of 6-gingerol, a bioactive compound from ginger, in overcoming TMZ resistance in GBM and delineates its molecular mechanisms. TMZ-resistant GBM cell lines (U87-TR and A172-TR) were established which exhibited enhanced migratory capacity and pronounced epithelial-mesenchymal transition (EMT) features. Treatment with 6-gingerol significantly reduced cell viability, colony formation, and migratory ability, as demonstrated by wound healing and transwell assays. Co-treatment with TMZ and 6-gingerol restored TMZ sensitivity and enhanced cytotoxicity in resistant cells. Mechanistically, 6-gingerol suppressed matrix metalloproteinases (MMP-2 and MMP-9) and reversed EMT, as indicated by the upregulation of epithelial markers and downregulation of mesenchymal markers. Western blot and transcriptomic analyses revealed activation of the PI3K/Akt/GSK-3β pathway and overexpression of β-catenin and c-Myc in TMZ-resistant cells. 6-Gingerol inhibited PI3K/Akt phosphorylation and downstream targets, notably reducing c-Myc levels. Pharmacological intervention confirmed that PI3K/Akt signaling governs c-Myc expression and EMT progression in TMZ-resistant GBM. In vivo, 6-gingerol markedly suppressed tumor growth in a TMZ-resistant xenograft model without observable toxicity, accompanied by inhibition of the PI3K/Akt/β-catenin/c-Myc axis. These findings demonstrate that 6-gingerol effectively reverses TMZ resistance and EMT-driven invasiveness, supporting its potential as a novel adjuvant strategy in GBM therapy.

Keywords: 6-gingerol; EMT; GBM; Migratory ability; PI3K/Akt signaling pathway; TMZ resistance.

MeSH terms

  • Animals
  • Brain Neoplasms* / drug therapy
  • Brain Neoplasms* / metabolism
  • Brain Neoplasms* / pathology
  • Catechols* / pharmacology
  • Catechols* / therapeutic use
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Drug Resistance, Neoplasm / drug effects
  • Epithelial-Mesenchymal Transition / drug effects
  • Fatty Alcohols* / pharmacology
  • Fatty Alcohols* / therapeutic use
  • Glioblastoma* / drug therapy
  • Glioblastoma* / metabolism
  • Glioblastoma* / pathology
  • Humans
  • Mice
  • Mice, Nude
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins c-myc / metabolism
  • Signal Transduction / drug effects
  • Temozolomide* / pharmacology
  • Temozolomide* / therapeutic use
  • Xenograft Model Antitumor Assays
  • beta Catenin / metabolism

Substances

  • gingerol
  • Catechols
  • Fatty Alcohols
  • Proto-Oncogene Proteins c-akt
  • beta Catenin
  • Temozolomide
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-myc
  • CTNNB1 protein, human
  • MYC protein, human