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.
引用
收藏
页码:29 / 34
页数:6
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