化学
药品
药理学
药物输送
巴基斯坦卢比
常用化疗药物
癌症研究
医学
生物化学
新陈代谢
糖酵解
丙酮酸激酶
细胞凋亡
有机化学
作者
Cheng Qian,Yueke Zhou,Teng Zhang,Guanglu Dong,Mengyao Song,Yu Tang,Zhonghong Wei,Suyun Yu,Qiuhong Shen,Wenxing Chen,Jaesung P. Choi,Juming Yan,Chongjin Zhong,Li Wan,Jia Li,Aiyun Wang,Yin Lu,Yang Zhao
标识
DOI:10.1016/j.apsb.2024.02.003
摘要
Aberrant tumor blood vessels are prone to propel the malignant progression of tumors, and targeting abnormal metabolism of tumor endothelial cells emerges as a promising option to achieve vascular normalization and antagonize tumor progression. Herein, we demonstrated that salvianic acid A (SAA) played a pivotal role in contributing to vascular normalization in the tumor-bearing mice, thereby improving delivery and effectiveness of the chemotherapeutic agent. SAA was capable of inhibiting glycolysis and strengthening endothelial junctions in the human umbilical vein endothelial cells (HUVECs) exposed to hypoxia. Mechanistically, SAA was inclined to directly bind to the glycolytic enzyme PKM2, leading to a dramatic decrease in endothelial glycolysis. More importantly, SAA improved the endothelial integrity via activating the β-Catenin/Claudin-5 signaling axis in a PKM2-dependent manner. Our findings suggest that SAA may serve as a potent agent for inducing tumor vascular normalization.
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