Radiation-induced cell death mechanisms

被引:507
作者
Eriksson, David [1 ]
Stigbrand, Torgny [1 ]
机构
[1] Umea Univ, Dept Immunol, S-90185 Umea, Sweden
关键词
Radiation; Therapy; Apoptosis; Senescence; Mitotic catastrophe; p53; HELA HEP2 CELLS; WILD-TYPE P53; ACUTE LYMPHOBLASTIC-LEUKEMIA; BH3-ONLY PROTEINS PUMA; PROSTATE-CANCER CELLS; DNA-DAMAGE RESPONSE; BREAST-TUMOR CELLS; INDUCED APOPTOSIS; MITOTIC CATASTROPHE; IONIZING-RADIATION;
D O I
10.1007/s13277-010-0042-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:363 / 372
页数:10
相关论文
共 143 条
[1]   Reasons to reconsider the significance of apoptosis for cancer therapy [J].
Abend, M .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2003, 79 (12) :927-941
[2]   A comprehensive study of p53 transcriptional activity in thymus and spleen of γ irradiated mouse:: High sensitivity of genes involved in the two main apoptotic pathways [J].
Alvarez, Sandra ;
Drane, Pascal ;
Meiller, Anne ;
Bras, Marlene ;
Deguin-Chambon, Valerie ;
Bouvard, Veronique ;
May, Evelyne .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2006, 82 (11) :761-770
[3]   Living with p53, dying of p53 [J].
Aylon, Yael ;
Oren, Moshe .
CELL, 2007, 130 (04) :597-600
[4]   Structural and Functional Basis for Therapeutic Modulation of p53 Signaling [J].
Bassett, Emily A. ;
Wang, Wenge ;
Rastinejad, Farzan ;
El-Deiry, Wafik S. .
CLINICAL CANCER RESEARCH, 2008, 14 (20) :6376-6386
[5]   DESMOID TUMORS IN ADULTS - THE ROLE OF RADIOTHERAPY IN THEIR MANAGEMENT [J].
BATAINI, JP ;
BELLOIR, C ;
MAZABRAUD, A ;
PILLERON, JP ;
CARTIGNY, A ;
JAULERRY, C ;
GHOSSEIN, NA .
AMERICAN JOURNAL OF SURGERY, 1988, 155 (06) :754-760
[6]   Radiation-induced acute immediate nuclear abnormalities in oral cancer cells -: Serial cytologic evaluation [J].
Bhattathiri, NV ;
Bindu, L ;
Remani, P ;
Chandralekha, B ;
Nair, KM .
ACTA CYTOLOGICA, 1998, 42 (05) :1084-1090
[7]   Prediction of radiosensitivity of oral cancers by serial cytological assay of nuclear changes [J].
Bhattathiri, NV ;
Bharathykkutty, C ;
Prathapan, R ;
Chirayathmanjiyil, DA ;
Nair, KM .
RADIOTHERAPY AND ONCOLOGY, 1998, 49 (01) :61-65
[8]   Cytostatic activity of paclitaxel in coronary artery smooth muscle cells is mediated through transient mitotic arrest followed by permanent post-mitotic arrest - Comparison with cancer cells [J].
Blagosklonny, Mikhail V. ;
Demidenko, Zoya N. ;
Giovino, Maria ;
Szynal, Carmin ;
Donskoy, Elina ;
Herrmann, Robert A. ;
Barry, James J. ;
Whalen, Anne M. .
CELL CYCLE, 2006, 5 (14) :1574-1579
[9]   DNA damage induces Chk1-dependent centrosome amplification [J].
Bourke, Emer ;
Dodson, Helen ;
Merdes, Andreas ;
Cuffe, Lorraine ;
Zachos, George ;
Walker, Mark ;
Gillespie, David ;
Morrison, Ciaran G. .
EMBO REPORTS, 2007, 8 (06) :603-609
[10]   Awakening guardian angels: drugging the p53 pathway [J].
Brown, Christopher J. ;
Lain, Sonia ;
Verma, Chandra S. ;
Fersht, Alan R. ;
Lane, David P. .
NATURE REVIEWS CANCER, 2009, 9 (12) :862-873