Effect of Metformin in Combination With Trametinib and Paclitaxel on Cell Survival and Metastasis in Melanoma Cells

Anticancer Res. 2021 Mar;41(3):1387-1399. doi: 10.21873/anticanres.14896.

Abstract

Background/aim: Despite clinical benefit from treatment with dabrafenib and trametinib in melanoma patients with BRAF mutations, half relapse within months and one-third are unresponsive to treatment. We evaluated the anticancer potential of metformin in combination with trametinib plus paclitaxel, against four melanoma cell lines.

Materials and methods: Metformin with trametinib and paclitaxel was tested for effects on cell viability, signaling molecules in MAPK and mTOR pathways, factors involved in epithelial-mesenchymal transition (EMT), and cell motility.

Results: The combination of metformin with trametinib and paclitaxel showed differential growth inhibitory effects; synergistic effects were observed in a cell line in which metformin suppresses ERK activity, whereas the combination showed antagonistic effects in a cell line with metformin-induced ERK activation. Trametinib or paclitaxel increased the expression of EMT regulators and melanoma cell motility, which were suppressed by combining metformin with trametinib and paclitaxel.

Conclusion: The combined treatment of metformin with trametinib and paclitaxel showed divergent effects on melanoma cell viability. Metformin might be useful as a potential adjuvant against cell proliferation and metastatic activity in melanoma patients.

Keywords: Metformin; combined treatment; melanoma cell; paclitaxel; trametinib.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Drug Synergism
  • Epithelial-Mesenchymal Transition / drug effects
  • Humans
  • Melanoma / genetics
  • Melanoma / metabolism
  • Melanoma / pathology*
  • Metformin / pharmacology*
  • Mutation
  • Paclitaxel / pharmacology*
  • Proto-Oncogene Proteins B-raf / genetics
  • Pyridones / pharmacology*
  • Pyrimidinones / pharmacology*
  • Signal Transduction / drug effects
  • Skin Neoplasms / genetics
  • Skin Neoplasms / metabolism
  • Skin Neoplasms / pathology*

Substances

  • Antineoplastic Agents
  • Pyridones
  • Pyrimidinones
  • trametinib
  • Metformin
  • Proto-Oncogene Proteins B-raf
  • Paclitaxel