The role of the stress-activated protein kinase (SAPK/JNK) signaling pathway in radiation-induced apoptosis

被引:85
作者
Verheij, M
Ruiter, GA
Zerp, SF
van Blitterswijk, WJ
Fuks, Z
Haimovitz-Friedman, A
Bartelink, H
机构
[1] Netherlands Canc Inst, Dept Radiotherapy, Antoni van Leeuwenhoek Huis, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Div Cellular Biochem, Antoni van Leeuwenhoek Huis, NL-1066 CX Amsterdam, Netherlands
[3] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10021 USA
关键词
SAPK/JNK; radiation; stress; signal transduction; apoptosis;
D O I
10.1016/S0167-8140(98)00007-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ionizing radiation, like a variety of other cellular stress factors, initiates apoptosis, or programmed cell death, in many cell systems. This mode of radiation-induced cell kill should be distinguished from clonogenic cell death due to unrepaired DNA damage. Ionizing radiation not only exerts its effect on the nuclear DNA, but also at the plasma membrane level where it may activate multiple signal transduction pathways. One of these pathways is the stress-activated protein kinase (SAPK) cascade which transduces death signals from the cell membrane to the nucleus. This review discusses recent evidence on the critical role of this signaling system in radiation-and stress-induced apoptosis. An improved understanding of the mechanisms involved in radiation-induced apoptosis may ultimately provide novel strategies of intervention in specific signal transduction pathways to favorably alter the therapeutic ratio in the treatment of human malignancies. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:225 / 232
页数:8
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