Accumulation of the cell cycle regulators TP53 and CDKN1A (p21) in human fibroblasts after exposure to low- and high-LET radiation

被引:44
作者
Fournier, C [1 ]
Wiese, C [1 ]
Taucher-Scholz, G [1 ]
机构
[1] GSI Biophys, D-64291 Darmstadt, Germany
关键词
D O I
10.1667/RR3182
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The accumulation of the cell cycle regulators TP53 and CDKN1A (p21/CIP1/WAF1) was investigated after exposure to X rays and carbon ions (170 keV mum(-1)) and xenon, bismuth and uranium ions (8900-15,000 keV mum(-1)) in normal human fibroblasts. The influence of the overall dose and the LET of these radiation types was studied systematically and the kinetics of the cell response was followed up to 24 h after exposure. The accumulation of TP53 protein was dependent on the dose and the LET, and TP53 levels declined to lower levels for all radiation types within 24 h after exposure. CDKN1A levels increased and peaked at 3 to 6 h after exposure. The persisting level of this protein at 24 h was strongly dependent on the dose and the LET for X rays and carbon ions. The exposure to very high-LET ions (8900-15,000 keV mum(-1)) did not lead to a further increase in CDKN1A, suggesting a saturation effect for the induction of this protein. The cellular effects of elevated CDKN1A after particle irradiation are discussed. (C) 2004 by Radiation Research Society.
引用
收藏
页码:675 / 684
页数:10
相关论文
共 62 条
[1]   P53 CONTROLS BOTH THE G(2)/M AND THE G(1) CELL-CYCLE CHECKPOINTS AND MEDIATES REVERSIBLE GROWTH ARREST IN HUMAN FIBROBLASTS [J].
AGARWAL, ML ;
AGARWAL, A ;
TAYLOR, WR ;
STARK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) :8493-8497
[2]   Direct evidence for the participation of gap junction-mediated intercellular communication in the transmission of damage signals from α-particle irradiated to nonirradiated cells [J].
Azzam, EI ;
de Toledo, SM ;
Little, JB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :473-478
[3]  
Azzam EI, 2000, CANCER RES, V60, P2623
[4]  
BAILY NTJ, 1981, STAT METHODS BIOL
[5]  
Balcer-Kubiczek EK, 1999, INT J RADIAT BIOL, V75, P529, DOI 10.1080/095530099140177
[6]   P53 MUTATIONAL STATUS AND SURVIVAL OF HUMAN BREAST-CANCER MCF-7 CELL VARIANTS AFTER EXPOSURE TO X-RAYS OR FISSION NEUTRONS [J].
BALCERKUBICZEK, EK ;
YIN, J ;
LIN, K ;
HARRISON, GH ;
ABRAHAM, JM ;
MELTZER, SJ .
RADIATION RESEARCH, 1995, 142 (03) :256-262
[7]   Mammalian G1- and S-phase checkpoints in response to DNA damage [J].
Bartek, J ;
Lukas, J .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (06) :738-747
[8]   Heavy-ion radiobiology: New approaches to delineate mechanisms underlying enhanced biological effectiveness [J].
Blakely, EA ;
Kronenberg, A .
RADIATION RESEARCH, 1998, 150 (05) :S126-S145
[9]   Cell cycle - Piecing together the p53 puzzle [J].
Carr, AM .
SCIENCE, 2000, 287 (5459) :1765-1766
[10]  
Daino K, 2002, RADIAT RES, V157, P478, DOI 10.1667/0033-7587(2002)157[0478:EIOCPA]2.0.CO