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靶向肿瘤细胞中的神经酰胺系统。

Targeting the ceramide system in cancer.

机构信息

Dept. of Molecular Biology, University of Duisburg-Essen, Hufelandstrasse 55, 45 122 Essen, Germany.

出版信息

Cancer Lett. 2013 May 28;332(2):286-94. doi: 10.1016/j.canlet.2011.07.010. Epub 2011 Jul 23.

Abstract

Sphingolipids, in particular ceramide, have been described as important components of cellular signalling pathways. Ceramide can be produced via multiple mechanisms including through the hydrolysis of sphingomyelin by acid and neutral sphingomyelinase or by a de novo synthesis pathway. Recent studies have identified sphingomyelinases and ceramide synthases as important targets for γ-irradiation and chemotherapeutic drugs. Likewise, common cancer treatment modalities, such as γ-irradiation and many chemotherapeutic agents, induce cell death via the generation of ceramide. This suggests that the manipulation of ceramide production and metabolism could offer promising means for the enhancement of anti-tumor therapies. The focus of this mini-review will be to discuss contemporary evidence suggesting that ceramide forming pathways and ceramide itself are important targets for the treatment of tumors and the development of novel tumor treatment strategies.

摘要

鞘脂类,特别是神经酰胺,已被描述为细胞信号通路的重要组成部分。神经酰胺可以通过多种机制产生,包括通过酸性和中性鞘磷脂酶水解鞘磷脂,或通过从头合成途径。最近的研究已经确定了鞘磷脂酶和神经酰胺合酶是γ-辐射和化疗药物的重要靶点。同样,常见的癌症治疗方式,如γ-辐射和许多化疗药物,通过产生神经酰胺诱导细胞死亡。这表明,神经酰胺生成和代谢的操纵可能为增强抗肿瘤治疗提供有前途的手段。本综述的重点将讨论当代证据,表明神经酰胺形成途径和神经酰胺本身是治疗肿瘤和开发新的肿瘤治疗策略的重要靶点。

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