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Metformin Induces Human Esophageal Carcinoma Cell Pyroptosis by Targeting the miR-497/PELP1 Axis

  • Lu Wang
  • , Kai Li
  • , Xianjie Lin
  • , Zhimeng Yao
  • , Shuhong Wang
  • , Xiao Xiong
  • , Zhifeng Ning
  • , Jing Wang
  • , Xiaozheng Xu
  • , Yi Jiang
  • , Ditian Liu
  • , Yuping Chen
  • , Dianzheng Zhang
  • , Hao Zhang

Research output: Contribution to journalArticlepeer-review

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.

Original languageAmerican English
JournalCancer letters
Volume450
StatePublished - Feb 13 2019

Keywords

  • Chemotherapy resistance
  • GSDMD
  • Metformin
  • Pyroptosis
  • miR-497

Disciplines

  • Medicine and Health Sciences
  • Oncology

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