Table 2 Ferroptosis inducers that could be radiosensitizer.
Compound | Classification | Target | Cell line | Mechanism |
|---|---|---|---|---|
Artesunate | Class IV | ROS | These cell lines include the human pancreatic duct epithelial HPDE cell line, human embryonic kidney 293T cell lines, and four pancreatic adenocarcinoma cell lines (Panc-1, COLO357, AsPC-1, and BxPC-3). | Endogenous Fe2+ causes the cleavage of endoperoxide bridge, and leads to the generation of ROS |
Buthionine sulfoximine (BSO) | Class I | GSH | 4T1 cell | Inhibit GSH synthesis |
Cisplatin | Class I | GSH | Cell lines include colorectal cancer (HCT116), fibrosarcoma (HT-1080), and non-small cell lung cancer (NSCLC) (A549, NCIH358, NCIH460, and Calu-1) | Inhibit GSH synthesis |
Dihydroartemisinin (DHA) | Class IV | ROS | Human hepatocyte cell line HL-7702, human umbilical vein endothelial cells (HUVECs), human laryngeal carcinoma HEP-2, human nasopharyngeal carcinoma cell lines (5-8F, CNE-1, CNE-2, CNE-2Z), and a non-cancerous immortalized nasopharyngeal epithelial cell line NP-69 | Endogenous Fe2+ causes the cleavage of endoperoxide bridge, and leads to the generation of ROS |
Erastin | Class I | SLC7A11 | The following human cell lines were used: A549, H460, H1299, and H23 for non-small cell lung cancer; MCF-7 for breast adenocarcinoma; HT-1080 for fibrosarcoma; FLO-1 for esophageal adenocarcinoma; UMRC6 for renal carcinoma; and human embryonic kidney 293 (HEK293T) cells | Inhibit SLC7A11 activity |
Ferroptocide | Class IV | Thioredoxin | ES-2 (ovarian cancer) cell line and HCT 116 cell lines | Inhibit thioredoxin |
FIN56 | Class III | CoQ, GPX4 | The following human cell lines were used: A549, H460, H1299, and H23 for non-small cell lung cancer; MCF-7 for breast adenocarcinoma; HT-1080 for fibrosarcoma; FLO-1 for esophageal adenocarcinoma; UMRC6 for renal carcinoma; and human embryonic kidney 293 (HEK293T) cells | Deplete CoQ and degrade GPX4 |
Imidazole ketone erastin (IKE) | Class I | SLC7A11 | The following cell lines are available: SUDHL-5 (female), SUDHL-6 (male), SUDHL-16 (male), HT-1080 (male), DOHH-2 (male), HBL-1 (male), U2932 (female), SUDHL-7 (male), SUDHL-9 (male), A4/FUK (female), WSU-NHL (female), Ly18 (OCI-Ly18) (male), Karpas422 (female), SUDHL-1 (male), SUDHL-2 (female), SUDHL-8 (male), SUDHL-10 (male), A3/KAW (female), RIVA (female), Ly9 (OCI-Ly9) (male), U937 (male), and Ly7 (OCI-Ly7) (male) | Inhibit SLC7A11 activity |
ML162 | Class II | GPX4 | The following human cell lines were used: A549, H460, H1299, and H23 for non-small cell lung cancer; MCF-7 for breast adenocarcinoma; HT-1080 for fibrosarcoma; FLO-1 for esophageal adenocarcinoma; UMRC6 for renal carcinoma; and human embryonic kidney 293 (HEK293T) cells | Inhibit GPX4 activity |
Nonthermal plasma | Class IV | ROS | Human lung cancer cell lines, Calu-1, H1299, H1975, HCC827, A549 and PC9 cells | Promote the release of Fe2+ from ferritin |
RSL3, (1S,3R)-RSL3 | Class II | GPX4 | The following human cell lines were used: A549, H460, H1299, and H23 for non-small cell lung cancer; MCF-7 for breast adenocarcinoma; HT-1080 for fibrosarcoma; FLO-1 for esophageal adenocarcinoma; UMRC6 for renal carcinoma; and human embryonic kidney 293 (HEK293T) cells | Inhibit GPX4 activity |
Salazosulfapyridine | Class I | SLC7A11 | The following human cell lines were used: A549, H460, H1299, and H23 for non-small cell lung cancer; MCF-7 for breast adenocarcinoma; HT-1080 for fibrosarcoma; FLO-1 for esophageal adenocarcinoma; UMRC6 for renal carcinoma; and human embryonic kidney 293 (HEK293T) cells | Inhibit SLC7A11 activity |
Salinomycin | Class IV | ROS | Human osteosarcoma U2OS cell line, human mammary epithelial cell line HMLER CD44high/CD24low cells, ICSCL-10A2 cells | Inhibit iron translocation and deplete ferritin |
Sorafenib | Class I | SLC7A11 | BJeH, BJeHLT, BJeLR, 143B, HT-1080 and Calu-1 cell lines | Inhibit SLC7A11 activity |
Withaferin A | Class II | GPX4 | IMR-32, SK-N-SH, Kelly, NB69, CHP-134, SH-EP, SH-SY5Y, SK-N-AS, SK-N-DZ, CHP-212 etc. cells | Inhibit GPX4 activity |