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CD95L/FasL与肿瘤坏死因子相关凋亡诱导配体在肿瘤监测与癌症治疗中的作用

CD95L/FasL and TRAIL in tumour surveillance and cancer therapy.

作者信息

Wajant Harald

机构信息

Department of Molecular Internal Medicine, Medical Polyclinic, University of Wuerzburg, Roentgenring 11, 97070 Wuerzburg, Germany.

出版信息

Cancer Treat Res. 2006;130:141-65. doi: 10.1007/0-387-26283-0_7.

Abstract

The membrane-bound death ligands CD95L/FasL and TRAIL, which activate the corresponding death receptors CD95/Fas, TRAILR1 and TRAILR2, induce apoptosis in many tumour cells, but can also elicit an inflammatory response. This chapter focuses on the relevance of CD95L/FasL and TRAIL for the tumour surveillance function of natural killer cells and cytotoxic T-cells and discuss current concepts of utilizing these ligands in tumour therapy.

摘要

膜结合死亡配体CD95L/FasL和TRAIL可激活相应的死亡受体CD95/Fas、TRAILR1和TRAILR2,在许多肿瘤细胞中诱导凋亡,但也可引发炎症反应。本章重点关注CD95L/FasL和TRAIL与自然杀伤细胞和细胞毒性T细胞的肿瘤监视功能的相关性,并讨论在肿瘤治疗中利用这些配体的当前概念。

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