放射治疗
核分裂突变
细胞凋亡
癌症研究
程序性细胞死亡
细胞周期
放射免疫疗法
衰老
有丝分裂
细胞
医学
细胞生长
细胞周期检查点
生物
免疫学
细胞生物学
内科学
遗传学
抗体
单克隆抗体
作者
David Eriksson,Torgny Stigbrand
出处
期刊:Tumor Biology
[SAGE]
日期:2010-05-19
卷期号:31 (4): 363-372
被引量:606
标识
DOI:10.1007/s13277-010-0042-8
摘要
The main goal when treating malignancies with radiation therapy is to deprive tumor cells of their reproductive potential. One approach to achieve this is by inducing tumor cell apoptosis. Accumulating evidences suggest that induction of apoptosis alone is insufficient to account for the therapeutic effect of radiotherapy. It has become obvious in the last few years that inhibition of the proliferative capacity of malignant cells following irradiation, especially with solid tumors, can occur via alternative cell death modalities or permanent cell cycle arrests, i.e., senescence. In this review, apoptosis and mitotic catastrophe, the two major cell deaths induced by radiation, are described and dissected in terms of activating mechanisms. Furthermore, treatment-induced senescence and its relevance for the outcome of radiotherapy of cancer will be discussed. The importance of p53 for the induction and execution of these different types of cell deaths is highlighted. The efficiency of radiotherapy and radioimmunotherapy has much to gain by understanding the cell death mechanisms that are induced in tumor cells following irradiation. Strategies to use specific inhibitors that will manipulate key molecules in these pathways in combination with radiation might potentiate therapy and enhance tumor cell kill.
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