The glycosphingolipid globotriaosylceramide in the metastatic transformation of colon cancer
摘要:
The most devastating aspect of cancer is the emergence of metastases. Thus, identification of potentially metastatic cells among a tumor cell population and the underlying molecular changes that switch cells to a metastatic state are among the most important issues in cancer biology. Here we show that although normal human colonic epithelial cells lack the glycosphingolipid globotriaosylceramide (Gb3) this molecule is highly expressed in metastatic colon cancer. In addition, a subpopulation of cells that are greatly enriched in Gb3and have an invasive phenotype was identified in human colon cancer cell lines. In epithelial cells in culture, Gb3was necessary and sufficient for cell invasiveness. Transfection of Gb3synthase, resulting in Gb3expression in non-cancerous polarized epithelial cells lacking endogenous Gb3induced cell invasiveness. Furthermore, Gb3knockdown by small inhibitory RNA in colon cancer epithelial cells inhibited cell invasiveness. Gb3is the plasma membrane receptor for Shiga toxin 1. The noncatalytic B subunit of Shiga toxin 1 causes apoptosis of human colon cancer cells expressing Gb3Injections of the B subunit of Shiga toxin 1 into HT29 human colon cancer cells engrafted into the flanks of nude mice inhibited tumor growth. These data demonstrate the appearance of a subpopulation of Gb3containing epithelial cells in the metastatic stage of human colon cancer and suggest their possible role in colon cancer invasiveness.
展开
关键词:
DOI:
10.1073/pnas.0506474102
被引量:
年份:
2005


































通过文献互助平台发起求助,成功后即可免费获取论文全文。
相似文献
参考文献
引证文献
研究点推荐
引用走势
辅助模式
引用
文献可以批量引用啦~
欢迎点我试用!