ETV4/ALYREF-mediated glycolytic metabolism through PKM2 enhances resistance to ferroptosis and promotes the development of intrahepatic cholangiocarcinoma

ETV4 promotes ICC development and ferroptosis resistance by facilitating glycolytic metabolism, and regulating PKM2 transcription by directly binding to the PKM2 promoter. Additionally, it mediates m5C-dependent PKM2 stabilization by directly binding to ALYREF. This study identified a new potential therapeutic target for ICC.

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Publication Details

Journal
Cancer & Metabolism
Published
2025-04-22
DOI
https://doi.org/10.1186/s40170-025-00387-1
Citations
7
Primary Topic
Cholangiocarcinoma and Gallbladder Cancer Studies
Type
article
Field-Weighted Citation Impact
14.04

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article

ETV4/ALYREF-mediated glycolytic metabolism through PKM2 enhances resistance to ferroptosis and promotes the development of intrahepatic cholangiocarcinoma

Zhongzhi Ma, Changjun Liu, Xianhai Mao, Hannah Yong Wen et al.
7 citations
Cancer & Metabolism
Cholangiocarcinoma and Gallbladder Cancer Studies
14.04
article

ETV4/ALYREF-mediated glycolytic metabolism through PKM2 enhances resistance to ferroptosis and promotes the development of intrahepatic cholangiocarcinoma

Zhongzhi Ma, Changjun Liu, Xianhai Mao, Hannah Yong Wen, Xiaohui Wang, Wenbin Duan
article en
7 citations

Abstract

ETV4 promotes ICC development and ferroptosis resistance by facilitating glycolytic metabolism, and regulating PKM2 transcription by directly binding to the PKM2 promoter. Additionally, it mediates m5C-dependent PKM2 stabilization by directly binding to ALYREF. This study identified a new potential therapeutic target for ICC.

Cancer & MetabolismVol. 13(1)
Central South University (CN), Hunan Cancer Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Zero hunger
Openalex Percentile: Top 1%
Cholangiocarcinoma and Gallbladder Cancer Studies
14.04
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