• NEDD4L overexpression in HUVECs suppresses proliferation and migration, while enhancing autophagy.
• NEDD4L promotes K48-linked ubiquitination and degradation of eEF1A1, a key mechanism in regulating endothelial cell function.
• Loss of endothelial NEDD4L enhances tumor growth and angiogenesis in vivo, underscoring its tumor-suppressive role.
• The NEDD4L-eEF1A1 axis represents a novel therapeutic target for cancer therapy by inhibiting angiogenesis.
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