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|Title:||Mequindox induced cellular DNA damage via generation of reactive oxygen species|
|Authors:||Liu, J;Ouyang, M;Jiang, J;Mu, P;Wu, J;Yang, Q;Zhang, C;Xu, W;Wang, L;Huen, MSY;Deng, Y|
|Publisher:||Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/gentox|
|Description:||Mequindox, a quinoxaline-N-dioxide derivative that possesses antibacterial properties, has been widely used as a feed additive in the stockbreeding industry in China. While recent pharmacological studies have uncovered potential hazardous effects of mequindox, exactly how mequindox induces pathological changes and the cellular responses associated with its consumption remain largely unexplored. In this study, we investigated the cellular responses associated with mequindox treatment. We report here that mequindox inhibits cell proliferation by arresting cells at the G2/M phase of the cell cycle. Interestingly, this mequindox-associated deleterious effect on cell proliferation was observed in human, pig as well as chicken cells, suggesting that mequindox acts on evolutionarily conserved target(s). To further understand the mequindox-host interaction and the mechanism underlying mequindox-induced cell cycle arrest, we measured the cellular content of DNA damage, which is known to perturb cell proliferation and compromise cell survival. Accordingly, using γ-H2AX as a surrogate marker for DNA damage, we found that mequindox treatment induced cellular DNA damage, which paralleled the chemical-induced elevation of reactive oxygen species (ROS) levels. Importantly, expression of the antioxidant enzyme catalase partially alleviated these mequindox-associated effects. Taken together, our results suggest that mequindox cytotoxicity is attributable, in part, to its role as a potent inducer of DNA damage via ROS. © 2011 Elsevier B.V.|
|Standard no:||Mutation Research - Genetic Toxicology And Environmental Mutagenesis, 2012, v. 741 n. 1-2, p. 70-75|
|Appears in Collections:||Department of Anatomy|
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