Genotoxicity of topoisomerase II inhibitors: An anti-infective perspective

被引:20
作者
Smart, Daniel J. [1 ]
机构
[1] GlaxoSmithKline R&D, Genet Toxicol, Ware SG12 0DP, Herts, England
关键词
Anti-infective agents; Topoisomerase II; DNA double-strand breaks; DNA damage response; gamma H2AX; Genotoxicity thresholds;
D O I
10.1016/j.tox.2008.08.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
At present, an inevitable consequence of a chemical's inhibitory activity on key regulators of DNA topology in bacteria, the type II topoisomerases, is a less pronounced effect on their eukaryotic counterparts. In the context of anti-infectives drug development, this may pose a risk to patient safety as inhibition of eukaryotic type II topoisomerases (TOPO II) can result in the generation of DNA double-strand breaks (DSBs), which have the potential to manifest as mutations, chromosome breakage or cell death. The biological effects of several TOPO II inhibitors in mammalian cells are described herein; their modulation of DSB damage response parameters is examined and evidence for the existence of a threshold concept for genotoxicity and its relevance in safety assessment is discussed. The potential utility of gamma H2AX, a promising and highly sensitive molecular marker for DSBs, in a novel genotoxicity 'pre-screen' to conventional assays is also highlighted. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:192 / 198
页数:7
相关论文
共 84 条
[11]   Antibacterial drug discovery in the 21st century [J].
Bush, K .
CLINICAL MICROBIOLOGY AND INFECTION, 2004, 10 :10-17
[12]   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
[13]   Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks [J].
Celeste, A ;
Fernandez-Capetillo, O ;
Kruhlak, MJ ;
Pilch, DR ;
Staudt, DW ;
Lee, A ;
Bonner, RF ;
Bonner, WM ;
Nussenzweig, A .
NATURE CELL BIOLOGY, 2003, 5 (07) :675-U51
[14]   Genomic instability in mice lacking histone H2AX [J].
Celeste, A ;
Petersen, S ;
Romanienko, PJ ;
Fernandez-Capetillo, O ;
Chen, HT ;
Sedelnikova, OA ;
Reina-San-Martin, B ;
Coppola, V ;
Meffre, E ;
Difilippantonio, MJ ;
Redon, C ;
Pilch, DR ;
Olaru, A ;
Eckhaus, M ;
Camerini-Otero, RD ;
Tessarollo, L ;
Livak, F ;
Manova, K ;
Bonner, WM ;
Nussenzweig, MC ;
Nussenzweig, A .
SCIENCE, 2002, 296 (5569) :922-927
[15]   DNA double-strand break repair signalling:: The case of RAD51 post-translational regulation [J].
Daboussi, F ;
Dumay, A ;
Delacôte, F ;
Lopez, BS .
CELLULAR SIGNALLING, 2002, 14 (12) :969-975
[16]  
DARPA P, 1990, CANCER RES, V50, P6919
[17]  
Degrassi Francesca, 2004, Current Medicinal Chemistry - Anti-Cancer Agents, V4, P317, DOI 10.2174/1568011043352920
[18]   Indications for a threshold of chemically-induced aneuploidy in vitro in human lymphocytes [J].
Elhajouji, A ;
VanHummelen, P ;
KirschVolders, M .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1995, 26 (04) :292-304
[19]   Indication for thresholds of chromosome non-disjunction versus chromosome lagging induced by spindle inhibitors in vitro in human lymphocytes [J].
Elhajouji, A ;
Tibaldi, F ;
KirschVolders, M .
MUTAGENESIS, 1997, 12 (03) :133-140
[20]   Quinolones share a common interaction domain on topoisomerase II with other DNA cleavage-enhancing antineoplastic drugs [J].
Elsea, SH ;
Westergaard, M ;
Burden, DA ;
Lomenick, JP ;
Osheroff, N .
BIOCHEMISTRY, 1997, 36 (10) :2919-2924