Liu Kuiliang, Fan Jianghao, Wu Jing
Department of Gastroenterology, Beijing Shijitan Hospital, Capital Medical University.
Drug Discov Ther. 2017;11(4):212-217. doi: 10.5582/ddt.2017.01017.
Sushi repeat-containing protein X-linked 2 (SRPX2) is a newly identified chondroitin sulfate proteoglycan that is markedly elevated in multiple solid tumors. It is also suggested that SRPX2 is associated with angiogenesis. A conditioned medium of SRPX2 overexpressing colorectal cancer (CRC) cells and SRPX2 recombinant protein was used to evaluate the effect of secretory SRPX2 on the angiogenesis ability of human umbilical vein endothelial cells (HUVECs) and the involved molecular mechanisms. It was revealed that the activity of SRPX2 is dependent on the urokinase-type plasminogen activator receptor and cooperation of the integrin αvβ3 co-receptor. Subsequent studies showed that both PI3K/Akt and Ras/MAPK pathways and phosphorylation of focal adhesion kinase is involved in the intracellular signaling pathway of SRPX2/uPAR. This study suggests that SRPX2 promotes angiogenesis of HUVECs through the cooperation of the uPAR and integrin/FAK pathway.
含寿司重复序列的X连锁蛋白2(SRPX2)是一种新发现的硫酸软骨素蛋白聚糖,在多种实体瘤中显著升高。也有研究表明SRPX2与血管生成有关。使用SRPX2过表达的结肠直肠癌(CRC)细胞条件培养基和SRPX2重组蛋白来评估分泌型SRPX2对人脐静脉内皮细胞(HUVECs)血管生成能力的影响及其相关分子机制。结果显示,SRPX2的活性依赖于尿激酶型纤溶酶原激活物受体以及整合素αvβ3共受体的协同作用。后续研究表明,PI3K/Akt和Ras/MAPK信号通路以及粘着斑激酶的磷酸化均参与了SRPX2/uPAR的细胞内信号通路。本研究提示,SRPX2通过uPAR与整合素/FAK信号通路的协同作用促进HUVECs的血管生成。