Effects of chemopreventive natural products on non-homologous end-joining DNA double-strand break repair

被引:25
作者
Charles, Catherine [1 ]
Nachtergael, Amandine [1 ]
Ouedraogo, Moustapha [2 ]
Belayew, Alexandra [3 ]
Duez, Pierre [1 ,4 ]
机构
[1] Univ Mons UMONS, Inst Hlth Sci & Technol, Dept Therapeut Chem & Pharmacognosy, B-7000 Mons, Belgium
[2] Univ Ouagadougou, Lab Pharmacol & Toxicol, Fac Hlth Sci, Ouagadougou 03, Burkina Faso
[3] Univ Mons UMONS, Mol Biol Lab, Inst Hlth Sci & Technol, B-7000 Mons, Belgium
[4] Univ Libre Bruxelles, Lab Pharmacognosy Bromatol & Human Nutr, Fac Pharm, B-1050 Brussels, Belgium
关键词
Chemoprevention; Flavonoids; Arbutin; Curcumin; Indole-3-carbinol; Microelectrophoresis; INDUCED APOPTOSIS; CANCER PREVENTION; GENE-EXPRESSION; BACKUP PATHWAYS; TUMOR-CELLS; FLAVONOIDS; INDOLE-3-CARBINOL; QUERCETIN; PROTEIN; ASSAY;
D O I
10.1016/j.mrgentox.2014.04.014
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
Double-strand breaks (DSBs) may result from endogenous (e.g., reactive oxygen species, variable (diversity) joining, meiotic exchanges, collapsed replication forks, nucleases) or exogenous (e.g., ionizing radiation, chemotherapeutic agents, radiomimetic compounds) events. DSBs disrupt the integrity of DNA and failed or improper DSBs repair may lead to genomic instability and, eventually, mutations, cancer, or cell death. Non-homologous end-joining (NHEJ) is the major pathway used by higher eukaryotic cells to repair these lesions. Given the complexity of NHEJ and the number of proteins and cofactors involved, secondary metabolites from medicinal or food plants might interfere with the process, activating or inhibiting repair. Twelve natural products, arbutin, curcumin, indole-3-carbinol, and nine flavonoids (apigenin, baicalein, chalcone, epicatechin, genistein, myricetin, naringenin, quercetin, sakuranetin) were chosen for their postulated roles in cancer chemoprevention and/or treatment. The effects of these compounds on NHEJ were investigated with an in vitro protocol based on plasmid substrates. Plasmids were linearized by a restriction enzyme, generating cohesive ends, or by a combination of enzymes, generating incompatible ends; plasmids were then incubated with a nuclear extract prepared from normal human small-intestinal cells (FHS 74 Int), either treated with these natural products or untreated (controls). The NHEJ repair complex from nuclear extracts ligates linearized plasmids, resulting in plasmid oligomers that can be separated and quantified by on-chip microelectrophoresis. Some compounds (chalcone, epicatechin, myricetin, sakuranetin and arbutin) clearly activated NHEJ, whereas others (apigenin, baicalein and curcumin) significantly reduced the repair rate of both types of plasmid substrates. Although this in vitro protocol is only partly representative of the in vivo situation, the natural products appear to interfere with NHEJ repair and warrant further investigation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
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