HPV18 E6 inhibits α‐ketoglutarate‐induced pyroptosis of esophageal squamous cell carcinoma cells via the P53/MDH1/ROS/GSDMC pathway

Author:

Tang Duo1ORCID,Zheng Yuchen1,Wang Guozhen12,Sheng Chao1,Liu Zijia1,Wang Biqi1,Zong Qi1,Zhang Yuchen1,Hou Xiaonan1,Yao Mengfei1,Zhou Zhixiang1

Affiliation:

1. Beijing International Science and Technology Cooperation Base of Antivirus Drug, Department of Biology, Faculty of Environment and Life Beijing University of Technology Beijing China

2. Department of Clinical Laboratory China‐Japan Friendship Hospital Beijing China

Abstract

Oncogene E6 plays a critical role in the development and progression of esophageal cancer caused by human papillomavirus (HPV) infection. Alpha‐ketoglutarate (AKG) is a key metabolite in the tricarboxylic acid cycle and has been widely used as a dietary and anti‐ageing supplement. In this study, we found that treating esophageal squamous carcinoma cells with a high dose of AKG can induce cell pyroptosis. Furthermore, our research confirms that HPV18 E6 inhibits AKG‐induced pyroptosis of esophageal squamous carcinoma cells by lowering P53 expression. P53 downregulates malate dehydrogenase 1 (MDH1) expression; however, MDH1 downregulates L‐2‐hydroxyglutarate (L‐2HG) expression, which inhibits a rise in reactive oxygen species (ROS) levels—as L‐2HG is responsible for excessive ROS. This study reveals the actuating mechanism behind cell pyroptosis of esophageal squamous carcinoma cells induced by high concentrations of AKG, and we posit the molecular pathway via which the HPV E6 oncoprotein inhibits cell pyroptosis.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

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