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These findings suggest that surface-modified MPs may contribute to vascular injury by disrupting the endothelial barrier and eliciting inflammatory responses
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Many patients experience slower progress after nine to twelve months of therapy, although timing varies depending on adherence, dose optimization, and underlying metabolic conditions
In conclusion, our data reveal that targeting estrogen-regulated SLC7A11 and SLC3A2 enhances ferroptosis in ER+ breast cancer, offering a novel therapeutic option for patients with ER+ breast cancer, particularly those with endocrine resistance
However, they are not always the right option for everyone
