Fusaric acid induces oxidative stress and apoptosis in human cancerous oesophageal SNO cells

被引:26
作者
Devnarain, Nikita [1 ]
Tiloke, Charlette [1 ]
Nagiah, Savania [1 ]
Chuturgoon, Anil A. [1 ]
机构
[1] Univ KwaZulu Natal, Discipline Med Biochem, Durban, South Africa
基金
新加坡国家研究基金会;
关键词
Fusaric acid; Apoptosis; Oxidative stress; SNO oesophageal cancer cells; Caspases-3/7; -8; -9; CARCINOMA; GROWTH; MITOCHONDRIA; INHIBITION; MECHANISM; TOXICITY; CLEAVAGE; ZINC;
D O I
10.1016/j.toxicon.2016.12.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oesophageal cancer (OC) is a global problem incrementally incident among black South African males. The high incidence of OC may be due to the consumption of corn as a staple, often contaminated with mycotoxins. Fusaric acid (FA), a neglected mycotoxin, is known to disrupt mitochondrial energy metabolism, chelates divalent metal cations and induces cell death in plants. This study investigated FA induced cytotoxicity and apoptotic induction in the SNO OC cell line. Cells were treated with FA (IC50 = 78.81 mu g/mL; 24 h; MIT assay) and assayed for oxidative stress and membrane damage (TBARS, LDH cytotoxicity and glutathione), apoptotic induction (ATP levels, caspase-8,-9,-3/7 activities) (Luminometry), single strand DNA and nuclear fragmentation (Comet and Hoechst assay). Additionally, relative expression of pro- and anti-apoptotic proteins were determined (Western Blotting). Significant antioxidant depletion was consistent with a concomitant increase in ROS-induced lipid peroxidation and extracellular LDH levels. FA induced apoptosis by significantly increasing Bax expression and caspase-8, -9 and-3/7 activities whilst decreasing ATP levels and Bcl-2 expression. Further, FA significantly increased comet tail lengths, PARP-1 expression and late stage apoptotic body formation in SNO cells. This study shows that FA is cytotoxic and induces increased apoptosis in SNO cells. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4 / 11
页数:8
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