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Modulating the SDF-1/CXCL12-induced cancer cell growth and adhesion by sulfated K5 polysaccharides in vitro
被引:11
|作者:
Teng, Liping
[1
,2
]
Fu, Haitian
[3
]
Deng, Chao
[1
]
Chen, Jingxiao
[3
]
Chen, Jinghua
[2
,3
]
机构:
[1] Jiangnan Univ, Wuxi Med Sch, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Minist Educ, Key Lab Ind Biotechnol, Wuxi 214122, Peoples R China
[3] Jiangnan Univ, Sch Pharmaceut Sci, Wuxi 214122, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Escherichia coli K5 capsular polysaccharide;
Sulfation SDF-1/CXCL12;
Cell growth;
Cell adhesion;
HUMAN-ENDOTHELIAL-CELLS;
METASTASIS;
DERIVATIVES;
INVASION;
IDENTIFICATION;
PROLIFERATION;
MIGRATION;
MIMETICS;
CXCR4;
D O I:
10.1016/j.biopha.2015.05.009
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Stromal cell-derived factor-1 (SDF-1)/chemokine (CXC motif) ligand 12 (CXCL12) is involved in the process of tumor progression. Sulfated K5 polysaccharides have shown anti-cancer activity by acting on multiple targets, though it remains unclear whether sulfated K5 polysaccharides would disrupt SDF-1/CXCL12-stimulated cancer biology. This study aimed to investigate the effects of sulfated K5 polysaccharides on cell growth, adhesion in murine B16 melanoma cells and the underlying mechanism by targeting SDF-1/CXCL12. Results indicated that K5-NS, OS inhibited the proliferation of B16 melanoma cells, induced the cell cycle arrest mainly at the G0/G1 phase, and suppressed cancer cell proliferation or adhesion induced by SDF-1/CXCL12. It was possible that K5-NS, OS appeared to interact with CXCL12 and block the subsequent biological functions. This work suggests that the existence of O- and N-sulfate groups is more effective in targeting CXCL12 and exhibiting anti-cancer activity. (C) 2015 Elsevier Masson SAS. All rights reserved.
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页码:29 / 34
页数:6
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