| Literature DB >> 30771436 |
Lu Wang1, Kai Li1, Xianjie Lin2, Zhimeng Yao2, Shuhong Wang3, Xiao Xiong3, Zhifeng Ning3, Jing Wang4, Xiaozheng Xu3, Yi Jiang5, Ditian Liu4, Yuping Chen4, Dianzheng Zhang6, Hao Zhang7.
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.Entities:
Keywords: Chemotherapy resistance; GSDMD; Metformin; Pyroptosis; miR-497
Year: 2019 PMID: 30771436 DOI: 10.1016/j.canlet.2019.02.014
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679