Impact of the circadian clock on in vitro genotoxic risk assessment assays

被引:6
作者
Destici, Eugin [1 ]
Oklejewicz, Malgorzata [1 ]
Nijman, Romana [1 ]
Tamanini, Filippo [1 ]
van der Horst, Gijsbertus T. J. [1 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Genet, Ctr Biomed Genet, NL-3000 CA Rotterdam, Netherlands
关键词
Genotoxicity; DNA damage; Carcinogenesis; Risk assessment; Circadian clock; DNA-DAMAGE RESPONSE; GENE-EXPRESSION; BIOLOGICAL CLOCK; GANGLION-CELLS; TRANSCRIPTION; MELANOPSIN; RHYTHMS; MPER2; CYCLE; MOUSE;
D O I
10.1016/j.mrgentox.2009.09.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Our society expects safety assessment for drugs, chemicals, cosmetics, and foods, which to date cannot be achieved without the use of laboratory animals. At the same time, society aims at refining, reducing, and (ultimately) replacing animal testing. As a consequence, much effort is taken to establish alternatives, such as toxicogenomics-based risk assessment assays on cultured cells and tissues. Evidently, the properties of cells in vitro will considerably differ from the in vivo situation. This review will discuss the impact of the circadian clock, an internal time keeping system that drives 24-h rhythms in metabolism, physiology and behavior, on in vitro genotoxic risk assessment. Our recent observation that DNA damaging agents can synchronize the circadian clock of individual cells in culture (and as a consequence the cyclic expression of clock-controlled genes, comprising up to 10% of the transcriptome) implies that the circadian clock should not be neglected when developing cell or tissue-based alternatives for chronic rodent toxicity assays. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 94
页数:8
相关论文
共 88 条
[1]  
Akashi M, 2000, GENE DEV, V14, P645
[2]   Differential functions of mPer1, mPer2, and mPer3 in the SCN circadian clock [J].
Bae, K ;
Jin, XW ;
Maywood, ES ;
Hastings, MH ;
Reppert, SM ;
Weaver, DR .
NEURON, 2001, 30 (02) :525-536
[3]   Initiating cellular stress responses [J].
Bakkenist, CJ ;
Kastan, MB .
CELL, 2004, 118 (01) :9-17
[4]   Multiple signaling pathways elicit circadian gene expression in cultured Rat-1 fibroblasts [J].
Balsalobre, A ;
Marcacci, L ;
Schibler, U .
CURRENT BIOLOGY, 2000, 10 (20) :1291-1294
[5]   A serum shock induces circadian gene expression in mammalian tissue culture cells [J].
Balsalobre, A ;
Damiola, F ;
Schibler, U .
CELL, 1998, 93 (06) :929-937
[6]   DNA damage checkpoints: from initiation to recovery or adaptation [J].
Bartek, Jiri ;
Lukas, Jiri .
CURRENT OPINION IN CELL BIOLOGY, 2007, 19 (02) :238-245
[7]   Phototransduction by retinal ganglion cells that set the circadian clock [J].
Berson, DM ;
Dunn, FA ;
Takao, M .
SCIENCE, 2002, 295 (5557) :1070-1073
[8]   Circadian variation in the expression of cell-cycle proteins in human oral epithelium [J].
Bjarnason, GA ;
Jordan, RCK ;
Sothern, RB .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (02) :613-622
[9]   Circadian expression of clock genes in human oral mucosa and skin : Association with specific cell-cycle phases [J].
Bjarnason, GA ;
Jordan, RCK ;
Wood, PA ;
Li, Q ;
Lincoln, DW ;
Sothern, RB ;
Hrushesky, WJM ;
Ben-David, Y .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (05) :1793-1801
[10]   A REVIEW AND MATHEMATICAL-ANALYSIS OF CIRCADIAN-RHYTHMS IN CELL-PROLIFERATION IN MOUSE, RAT, AND HUMAN EPIDERMIS [J].
BROWN, WR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (02) :273-280