Prospective Application of Ferroptosis in Hypoxic Cells for Tumor Radiotherapy.
Jing SuQin ZhaoZhuangzhuang ZhengHuanhuan WangChenbin BianLingbin MengYing XinXin JiangPublished in: Antioxidants (Basel, Switzerland) (2022)
Radiation therapy plays an increasingly important role in cancer treatment. It can inhibit the progression of various cancers through radiation-induced DNA breakage and reactive oxygen species (ROS) overload. Unfortunately, solid tumors, such as breast and lung cancer, often develop a hypoxic microenvironment due to insufficient blood supply and rapid tumor proliferation, thereby affecting the effectiveness of radiation therapy. Restraining hypoxia and improving the curative effect of radiotherapy have become difficult problems. Ferroptosis is a new type of cell death caused by lipid peroxidation due to iron metabolism disorders and ROS accumulation. It plays an important role in both hypoxia and radiotherapy and can enhance the radiosensitivity of hypoxic tumor cells by amplifying oxidative stress or inhibiting antioxidant regulation. In this review, we summarize the internal relationship and related mechanisms between ferroptosis and hypoxia, thus exploring the possibility of inducing ferroptosis to improve the prognosis of hypoxic tumors.
Keyphrases
- cell death
- radiation induced
- radiation therapy
- cell cycle arrest
- oxidative stress
- locally advanced
- reactive oxygen species
- induced apoptosis
- endothelial cells
- signaling pathway
- early stage
- randomized controlled trial
- systematic review
- mental health
- rectal cancer
- stem cells
- dna damage
- squamous cell carcinoma
- endoplasmic reticulum stress
- fatty acid
- anti inflammatory
- ischemia reperfusion injury
- circulating tumor
- young adults
- quantum dots