淋巴
唾液酸
细胞生物学
细胞粘附
基因敲除
化学
帕西林
粘附
分子生物学
转染
生物
细胞
生物化学
病理
医学
基因
有机化学
作者
Shujing Wang,Xixi Chen,Anwen Wei,Xiao Yu,Bachir Niang,Jianing Zhang
出处
期刊:Tumor Biology
[SAGE Publishing]
日期:2014-10-10
卷期号:36 (2): 885-892
被引量:30
标识
DOI:10.1007/s13277-014-2638-x
摘要
The alterations of cell surface sialylation play a key role in tumor metastasis. Enhanced α2,6-sialylation on N-glycans results from overexpression of the sialyltransferase ST6Gal-I. Hca-F and Hca-P cells are murine hepatocarcinoma cell lines which metastasize only to the lymph nodes. Our previous study revealed that ST6Gal-I was involved in the adhesion of Hca-F cells to fibronectin. However, the roles of sialic acids in the adhesion of Hca-F cells to lymph nodes still remain poorly understood. In this study, we observed that expression levels of α2,6-linked sialic acids on Hca-F cells were higher compared to Hca-P cells. Knockdown of ST6Gal-I by small hairpin RNA (shRNA) transfection decreased the expression of α2,6-linked sialic acids and inhibited the adhesion of Hca-F cells to lymph nodes. The adhesion ability was reported to be mediated by siglec-2 which preferentially binds to α2,6-linked sialic acids, and in addition, ST6Gal-I knockdown inhibited the phosphorylated levels of focal adhesion kinase (FAK) and paxillin when cells were treated with siglec-2. Taken together, these results suggest that interaction of α2,6-linked sialic acids with siglec-2 might modulate the adhesion of hepatocarcinoma cells to lymph nodes through the FAK signaling pathway.
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