Metformin induces human esophageal carcinoma cell pyroptosis by targeting the miR-497/PELP1 axis

Cancer Lett. 2019 May 28:450:22-31. doi: 10.1016/j.canlet.2019.02.014. Epub 2019 Feb 13.

Abstract

Evasion of apoptosis is a major contributing factor to the development of chemo- and radiotherapy resistance. Therefore, activation of non-apoptotic programmed cell death (PCD) could be an effective alternative against apoptosis-resistant cancers. In this study, we demonstrated in vitro and in vivo that metformin can induce pyroptosis, a non-apoptotic PCD, in esophageal squamous cell carcinoma (ESCC), a commonly known chemo-refractory cancer, especially at its advanced stages. Proline-, glutamic acid- and leucine-rich protein-1 (PELP1) is a scaffolding oncogene and upregulated PELP1 in advanced stages of ESCC is highly associated with cancer progression and patient outcomes. Intriguingly, metformin treatment leads to gasdermin D (GSDMD)-mediated pyroptosis, which is abrogated by forced expression of PELP1. Mechanistically, metformin induces pyroptosis of ESCC by targeting miR-497/PELP1 axis. Our findings suggest that metformin and any other pyroptosis-inducing reagents could serve as alternative treatments for chemo- and radiotherapy refractory ESCC or other cancers sharing the same pyroptosis mechanisms.

Keywords: Chemotherapy resistance; GSDMD; Metformin; Pyroptosis; miR-497.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation / drug effects
  • Co-Repressor Proteins / biosynthesis
  • Co-Repressor Proteins / genetics
  • Co-Repressor Proteins / metabolism*
  • Disease Progression
  • Down-Regulation / drug effects
  • Esophageal Neoplasms / drug therapy*
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / pathology
  • Esophageal Squamous Cell Carcinoma / drug therapy*
  • Esophageal Squamous Cell Carcinoma / genetics
  • Esophageal Squamous Cell Carcinoma / metabolism
  • Esophageal Squamous Cell Carcinoma / pathology
  • Female
  • Humans
  • Male
  • Metformin / pharmacology*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Middle Aged
  • Neoplasm Staging
  • Pyroptosis / drug effects
  • Signal Transduction / drug effects
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Up-Regulation / drug effects

Substances

  • Co-Repressor Proteins
  • MIRN497 microRNA, human
  • MicroRNAs
  • PELP1 protein, human
  • Transcription Factors
  • Metformin