Liu Ge, Liu Ming, Wei Jianteng, Huang Haijuan, Zhang Yuyan, Zhao Jin, Xiao Lin, Wu Ning, Zheng Lanhong, Lin Xiukun
Institute of Oceanology, Chinese Academy of Sciences, 7 Nanhai Road, Qingdao 266071, China.
Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.
Mar Drugs. 2014 Mar 13;12(3):1530-44. doi: 10.3390/md12031530.
CS5931 is a novel polypeptide from Ciona savignyi with anticancer activities. Previous study in our laboratory has shown that CS5931 can induce cell death via mitochondrial apoptotic pathway. In the present study, we found that the polypeptide could inhibit angiogenesis both in vitro and in vivo. CS5931 inhibited the proliferation, migration and formation of capillary-like structures of HUVECs (Human Umbilical Vein Endothelial Cell) in a dose-dependent manner. Additionally, CS5931 repressed spontaneous angiogenesis of the zebrafish vessels. Further studies showed that CS5931 also blocked vascular endothelial growth factor (VEGF) production but without any effect on its mRNA expression. Moreover, CS5931 reduced the expression of matrix metalloproteinases (MMP-2 and MMP-9) both on protein and mRNA levels in HUVEC cells. We demonstrated that CS5931 possessed strong anti-angiogenic activity both in vitro and in vivo, possible via VEGF and MMPs. This study indicates that CS5931 has the potential to be developed as a novel therapeutic agent as an inhibitor of angiogenesis for the treatment of cancer.
CS5931是一种来自萨氏海鞘的具有抗癌活性的新型多肽。我们实验室之前的研究表明,CS5931可通过线粒体凋亡途径诱导细胞死亡。在本研究中,我们发现该多肽在体外和体内均能抑制血管生成。CS5931以剂量依赖的方式抑制人脐静脉内皮细胞(HUVEC)的增殖、迁移和毛细血管样结构的形成。此外,CS5931抑制斑马鱼血管的自发血管生成。进一步研究表明,CS5931还能阻断血管内皮生长因子(VEGF)的产生,但对其mRNA表达没有任何影响。此外,CS5931在蛋白质和mRNA水平上均降低了HUVEC细胞中基质金属蛋白酶(MMP - 2和MMP - 9)的表达。我们证明CS5931在体外和体内均具有强大的抗血管生成活性,可能是通过VEGF和MMPs发挥作用。本研究表明,CS5931有潜力作为一种新型治疗药物,作为血管生成抑制剂用于癌症治疗。