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This suggests that si-PGC-1 carried by LNP exhibits superior tissue penetration within the tumor and has a more extensive distribution compared to the unencapsulated si-PGC-1 group

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ROS also disrupt intercellular junction proteins (e.g., vascular endothelial cadherin, VE-cadherin) in vascular endothelial cells, impairing the endothelial barrier

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