3.8 Review

Killing cancer cells by poly-drug elevation of ceramide - A hypothesis whose time has come?

期刊

EUROPEAN JOURNAL OF BIOCHEMISTRY
卷 268, 期 2, 页码 193-204

出版社

WILEY
DOI: 10.1046/j.1432-1033.2001.01845.x

关键词

apoptosis; cancer chemotherapy; ceramide concentration; ceramide metabolism; glucosylceramide synthesis inhibition; hormone effects on ceramide; multidrug resistance; sphingomyelin-ceramide pathway

向作者/读者索取更多资源

Many papers have shown that sphingolipids control the balance in cells between growth and proliferation, and cell death by apoptosis. Sphingosine-1-phosphate (Sph1P) and glucosylceramide (GlcCer) induce proliferation processes, and ceramide (Cer), a metabolic intermediate between the two, induces apoptosis. In cancers, the balance seems to have come undone and it should be possible to kill the cells by enhancing the processes that lead to ceramide accumulation. The two control systems are intertwined, modulated by a variety of agents affecting the activities of the enzymes in Cer-GlcCer-Sph1P interdependence. It is proposed that successful cancer chemotherapy requires the use of many agents to elevate ceramide levels adequately. This review updates current knowledge of sphingolipid metabolism and some of the evidence showing that ceramide plays a causal role in apoptosis induction, as well as a chemotherapeutic agent.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据