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The term ferroptosis was formally proposed in 2012, with mechanistic studies demonstrating erastins dual action in HT-1080 fibrosarcoma models: mitochondrial voltage-dependent anion channel (VDAC) modulation and inhibition of the Xc system subunit solute carrier family 7 member 11 (SLC7A11), leading to glutathione depletion and iron-dependent lipid ROS accumulation ( A pivotal 2014 study established glutathione peroxidase 4 (GPX4) as the central regulator of ferroptosis, with therapeutic implications validated in tumor xenografts (Yang et al., 2014)
This is an updated review of the clinical diagnosis and treatment of fibroids
The vortex model may elucidate why a single treatment, such as antibiotics or anti-inflammatory drugs, yields only modest improvements in the clinical outcomes of bronchiectasis
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