Correlation between unirradiated cell TP53 protein levels and radiosensitivity in MOLT-4 cells

被引:18
作者
Nakano, H
Shinohara, K [1 ]
机构
[1] Univ Tokyo, Fac Med, Radiat Res Inst, Bunkyo Ku, Tokyo 1130033, Japan
[2] Tokyo Metropolitan Inst Med Sci, Dept Radiat Res, Bunkyo Ku, Tokyo 1138613, Japan
关键词
D O I
10.2307/3580207
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
MOLT-4 cells undergo apoptosis after X irradiation. A radiosensitive variant, MOLT-4N1, and a radioresistant variant, MOLT-4N2, have been studied with respect to their radiosensitivity and its relationship to the levels of TP53 protein (formerly known as p53). X irradiation induces apoptosis in both cell lines with the following difference: The induction of apoptosis in MOLT-4N2 cells occurred late's than in MOLT-4N1 cells as determined by the morphological changes and DNA fragmentation, The levels of cell death measured by the dye exclusion test coincided with, the levels of apoptosis in both cell lines, suggesting that radiation-induced cell killing is determined by the induction of apoptosis, Unirradiated MPOLT-4N1 cells contained a significantly higher intracellular level of TP53 protein and a much higher level of TP53 mRNA compared to MOLT-4N2 cells. X irradiation led to an accumulation of TP53 protein in both cell lines that was greater in MOLT-4N1 cells, This accumulation of TP53 protein preceded changes in DNA degradation and ladder-formation and in nuclear morphology. These results strongly suggest that the radiosensitivity of MOLT-4 cells correlates well with the unirradiated control levels of TP53 mRNA and TP53 protein, and that the quantitative levels of TP53 protein must reach a threshold for the cells to undergo apoptosis, (C) 1999 by Radiation Research Society.
引用
收藏
页码:686 / 693
页数:8
相关论文
共 57 条
[1]   Enhanced phosphorylation of p53 by ATN in response to DNA damage [J].
Banin, S ;
Moyal, L ;
Shieh, SY ;
Taya, Y ;
Anderson, CW ;
Chessa, L ;
Smorodinsky, NI ;
Prives, C ;
Reiss, Y ;
Shiloh, Y ;
Ziv, Y .
SCIENCE, 1998, 281 (5383) :1674-1677
[2]  
BREAK Y, 1993, EMBO J, V12, P461
[3]  
BROWN DG, 1993, J BIOL CHEM, V268, P3037
[4]   Activation of the ATM kinase by ionizing radiation and phosphorylation of p53 [J].
Canman, CE ;
Lim, DS ;
Cimprich, KA ;
Taya, Y ;
Tamai, K ;
Sakaguchi, K ;
Appella, E ;
Kastan, MB ;
Siliciano, JD .
SCIENCE, 1998, 281 (5383) :1677-1679
[5]   FREQUENT MUTATIONS IN THE P53 TUMOR SUPPRESSOR GENE IN HUMAN LEUKEMIA T-CELL LINES [J].
CHENG, J ;
HAAS, M .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5502-5509
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   ALTERNATIVE SPLICING OF THE P53 TUMOR-SUPPRESSOR GENE IN THE MOLT-4 T-LYMPHOBLASTIC LEUKEMIA-CELL LINE [J].
CHOW, VTK ;
QUEK, HH ;
TOCK, EPC .
CANCER LETTERS, 1993, 73 (2-3) :141-148
[8]   THYMOCYTE APOPTOSIS INDUCED BY P53-DEPENDENT AND INDEPENDENT PATHWAYS [J].
CLARKE, AR ;
PURDIE, CA ;
HARRISON, DJ ;
MORRIS, RG ;
BIRD, CC ;
HOOPER, ML ;
WYLLIE, AH .
NATURE, 1993, 362 (6423) :849-852
[9]  
FAN SJ, 1994, CANCER RES, V54, P5824
[10]  
FRITSCHE M, 1993, ONCOGENE, V8, P307