1. Targeting FTO induces colorectal cancer ferroptotic cell death by decreasing SLC7A11/GPX4 expression.
- Author
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Qiao, Yaya, Su, Meng, Zhao, Huifang, Liu, Huanle, Wang, Chenxi, Dai, Xintong, Liu, Lingling, Liu, Guangju, Sun, Huanran, Sun, Mingming, Wang, Jiyan, Li, Zhen, Fan, Jun, Zhang, Quan, Li, Chunshen, Situ, Fangmin, Xue, Jun, Jia, Zhenghu, Zhang, Chunze, and Zhang, Shuai
- Subjects
CELL death ,COLORECTAL cancer ,CANCER cells ,GLUTATHIONE peroxidase ,ADIPOSE tissues ,MUPIROCIN - Abstract
Ferroptosis is a newly identified iron-dependent form of death that is becoming increasingly recognized as a promising avenue for cancer therapy. N6-methyladenosine (m
6 A) is the most abundant reversible methylation modification in mRNA contributing to tumorigenesis. However, the crucial role of m6 A modification in regulating ferroptosis during colorectal cancer (CRC) tumorigenesis remains elusive. Herein, we find that m6 A modification is increased during ferroptotic cell death and correlates with the decreased m6 A demethylase fat mass and obesity-associated protein (FTO) expression. Functionally, we demonstrate that suppressing FTO significantly induces CRC ferroptotic cell death, as well as enhancing CRC cell sensitivity to ferroptosis inducer (Erastin and RSL3) treatment. Mechanistically, high FTO expression increased solute carrier family 7 member 11 (SLC7A11) or glutathione peroxidase 4 (GPX4) expressions in an m6 A-YTHDF2 dependent manner, thereby counteracting ferroptotic cell death stress. In addition, we identify Mupirocin as a novel inhibitor of FTO, and Mupirocin induces CRC ferroptosis and inhibits tumor growth. Clinically, the levels of FTO, SLC7A11, and GPX4, are highly correlated expression in CRC tissues. Our findings reveal that FTO protects CRC from ferroptotic cell death in promoting CRC tumorigenesis through triggering SLC7A11/GPX4 expression. [ABSTRACT FROM AUTHOR]- Published
- 2024
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