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CS5931, a Novel Polypeptide in Ciona savignyi, Represses Angiogenesis via Inhibiting Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloproteinases (MMPs)

文献类型: 外文期刊

作者: Liu, Ge 1 ; Liu, Ming 3 ; Wei, Jianteng 4 ; Huang, Haijuan 5 ; Zhang, Yuyan 5 ; Zhao, Jin 6 ; Xiao, Lin 7 ; Wu, Ning 1 ; Zhe 1 ;

作者机构: 1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China

2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China

3.Ocean Univ China, Sch Med & Pharm, Minist Educ, Key Lab Marine Drugs, Qingdao 266003, Peoples R China

4.Chinese Acad Sci, Lanzhou Inst Chem Phys, Lanzhou 730000, Peoples R China

5.Qingdao Univ Sci & Technol, Qingdao 266042, Peoples R China

6.Zhengzhou Univ, Dept Biotechnol, Zhengzhou 450001, Peoples R China

7.Qingdao Agr Univ, Qingdao 266109, Peoples R China

8.Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Qingdao 266071, Peoples R China

9.Capital Med Univ, Dept Pharmacol, Beijing 100069, Peoples R China

关键词: zebrafish;anti-angiogenesis;HUVECs;CS5931;VEGF and MMPs

期刊名称:MARINE DRUGS ( 影响因子:5.118; 五年影响因子:5.951 )

ISSN: 1660-3397

年卷期: 2014 年 12 卷 3 期

页码:

收录情况: SCI

摘要: 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.

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