Gene interfered-ferroptosis therapy for cancers.
Jinliang GaoTao LuoJinke WangPublished in: Nature communications (2021)
Although some effective therapies have been available for cancer, it still poses a great threat to human health and life due to its drug resistance and low response in patients. Here, we develop a ferroptosis-based therapy by combining iron nanoparticles and cancer-specific gene interference. The expression of two iron metabolic genes (FPN and LCN2) was selectively knocked down in cancer cells by Cas13a or microRNA controlled by a NF-κB-specific promoter. Cells were simultaneously treated by iron nanoparticles. As a result, a significant ferroptosis was induced in a wide variety of cancer cells. However, the same treatment had little effect on normal cells. By transferring genes with adeno-associated virus and iron nanoparticles, the significant tumor growth inhibition and durable cure were obtained in mice with the therapy. In this work, we thus show a cancer therapy based on gene interference-enhanced ferroptosis.
Keyphrases
- cell death
- genome wide
- cell cycle arrest
- genome wide identification
- induced apoptosis
- human health
- papillary thyroid
- dna methylation
- iron deficiency
- copy number
- cancer therapy
- risk assessment
- end stage renal disease
- genome wide analysis
- transcription factor
- newly diagnosed
- signaling pathway
- ejection fraction
- poor prognosis
- crispr cas
- oxidative stress
- chronic kidney disease
- climate change
- endoplasmic reticulum stress
- prognostic factors
- peritoneal dialysis
- genome editing
- type diabetes
- squamous cell carcinoma
- immune response
- mesenchymal stem cells
- adipose tissue
- diabetic rats
- cell therapy
- endothelial cells
- toll like receptor
- bioinformatics analysis