共 288 条
Death receptors in chemotherapy and cancer
被引:402
作者:

Debatin, KM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Childrens Hosp, D-89075 Ulm, Germany

Krammer, PH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Childrens Hosp, D-89075 Ulm, Germany
机构:
[1] Univ Childrens Hosp, D-89075 Ulm, Germany
[2] German Canc Res Ctr, D-69120 Heidelberg, Germany
来源:
关键词:
apoptosis;
death receptors;
CD95;
drugs;
resistance;
D O I:
10.1038/sj.onc.1207558
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Apoptosis, the cell's intrinsic death program, is a key regulator of tissue homeostasis. An imbalance between cell death and proliferation may result in tumor formation. Also, killing of cancer cells by cytotoxic therapies such as chemotherapy, gamma-irradiation or ligation of death receptors is predominantly mediated by triggering apoptosis in target cells. In addition to the intrinsic mitochondrial pathway, elements of death receptor signaling pathways have been implied to contribute to the efficacy of cancer therapy. Failure to undergo apoptosis in response to anticancer therapy may lead to resistance. Also, deregulated expression of death receptor pathway molecules may contribute to tumorigenesis and tumor escape from endogenous growth control. Understanding the molecular events that regulate apoptosis induced by anticancer therapy and how cancer cells evade apoptosis may provide new opportunities for pathway-based rational therapy and for drug development.
引用
收藏
页码:2950 / 2966
页数:17
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