From: Induction and application of ferroptosis in cancer therapy
Therapy | Treatment | Combination drugs | Mechanism | Tumour type | Refs |
---|---|---|---|---|---|
Chemotherapy | Sorafenib | siRNA | Inhibit the MT-1G and the system xc- | HCC, RCC, NSCLC, PDAC | |
Artemisinin | Iron | Increase the level of intracellular free iron | PDAC, AML, HNSCC | ||
Cyst(e)inase | FINs | Deplete extracellular cystine | PDAC, Prostate cancer, Chronic lymphocytic leukemia | ||
Statins | - | Reduce selenoproteins (such as GPX4) and CoQ10 biosynthesis | Breast Cancer | [138] | |
Radiotherapy | RT | FINs | Up-regulates ACSL4, inhibit SLC7A11 or GPX4 | Neuroblastoma, NSCLC, Fibrosarcoma, Melanoma, Breast Cancer, Cervical cancer | |
Immunotherapy | PD-L1 inhibitors | FINs | Releas IFNγ to reduce the uptake of cystine | Fibrosarcoma | [11] |
TGF-β inhibitors and PD-1 antibodies | FINs | Generate an immunogenic microenvironment and produce H2O2, promoting the Fenton reaction | Melanoma | [146] | |
Nanomedicine | Metal–Organic Frameworks (MOF) | – | Release iron | Mononuclear macrophage leukemia | [148] |
FePt-NP2 | Iron nanoparticles and cisplatin | Increase the sensitivity of cancer cells to cisplatin | Ovarian cancer | [117] | |
SRF@FeIIITA (SFT) | Fe3+ and TA, nanocrystals of SRF, | Inhibit GPX4 and generate ROS | Fibrosarcoma | [71] | |
Nano-delivery vehicle | WithaferinA, IKE | Improve solubility and biocompatibility, and increase accumulation | Neuroblastoma, DLBCL | ||
AMSNs | Target cancer by ASS and release Mn ion to consume GSH | HCC | [149] | ||
MON-p53 | Providie unstable iron, and deliver p53 to cells | Fibrosarcoma | [150] | ||
Ultra-small poly(ethylene glycol) coated silica nanoparticles | Transport of extracellular iron into the cell | NeuroblastomaHCC | [151] | ||
PDT | FINs | Produce ROS and consume O2 | OTSCC, Breast Cancer, HCC | ||
PTT | SRF@MPDA-SPIO, FPMF@CpGODN | Release iron and SRF, produce ROS and consume O2 | CRC, Breast Cancer |