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. 2022 Jun 30;10:860344. doi: 10.3389/fcell.2022.860344

TABLE 1.

Candidate substances and genes for inducing ferroptosis in gastric cancer.

Substances and Genes Target/Function Mechanism
Actinidia chinensis Planch (Gao et al., 2020) GPx4, SLC7A11 Induces ROS accumulation
Tanshinone IIA (Guan et al., 2020) Ptgs2, Chac1, p53, xCT Tanshinone IIA upregulates p53 expression and downregulates xCT expression; Tan IIA decreases intracellular glutathione and cysteine levels and increases the levels of intracellular ROS.
Tanshinone IIA (Ni et al., 2021a) SLC7A11 Induces ROS accumulation
Physcion 8-O-β-glucopyranoside (Niu et al., 2019) GLS2 Induces ROS accumulation
Erastin (Sun et al., 2020) Mitochondrial dysfunction Induces ROS accumulation
Erastin (Chen L. et al., 2020; Mao et al., 2021) SLC7A11 Induces ROS accumulation
Cysteine Dioxygenase 1 GPX4, maintains stability of mitochondrial morphology Mediates erastin (Hao et al., 2017); induces ROS accumulation
Exosomes miR-522 (Zhang et al., 2020) ALOX15 Leads to ALOX15 suppression, decreased lipid-ROS accumulation in cancer cells, and ultimately results in decreased chemosensitivity
SIRT6 (Cai et al., 2021) GPX4 Inhibits GPX4 activity, induces ROS accumulation
CPEB1 (Wang J. et al., 2021) Gpx4 Induces ROS accumulation
MiR-375 (Ni et al., 2021b) SLC7A11 Induces ROS accumulation