Effect of Food Additive Citric Acid on The Growth of Human Esophageal Carcinoma Cell Line EC109

Xiaoguang Chen, Q. Lv, Yumei Liu, W. Deng
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引用次数: 27

Abstract

Objective Today, esophageal cancer (EC) has become one of the most common cancer types in China. Therefore, new drug and therapeutic strategies are urgently needed to improve postoperative survival rate of patients with EC. As a food additive, several lines of evidence have shown that citric acid can be served as glycolysis suppressor to inhibit growth of some tumor cells. However, little is known about the effect of this organic acid on the growth of human esophageal carcinoma cell line, EC109. Materials and Methods In this experimental study, cell proliferation rate was determined using MTT assay. Apoptotic morphological changes were evaluated by fluorescent microscopy using Hoechst 33258 staining. Cell apoptosis rate and mitochondrial membrane potential (MMP) were detected using flow-cytometry. Effect of citric acid on cellular membrane permeability was assessed by measuring lactate dehydrogenase (LDH) activity, using LDH assay kit. Results Compared to the control group, there was a marked decrease in cells proliferation when the cells were treated with higher citric acid concentrations (800, 1600 μg/ml). Typical apoptotic morphology of EC109 cells was observed upon treatment with citric acid, such as chromatin condensation and appearance of apoptotic body. Cell apoptotic indexes were significantly increased (P<0.01) after treatment with citric acid at the concentration of 400-1600 μg/ml. Extracellular LDH activity and loss of MMP in all of the treated groups were significantly higher than control (P<0.05), in a dose-dependent manner. Conclusion These results suggest that citric acid prevents EC109 cell growth by inhibiting cell proliferation and inducing apoptosis, which perhaps offers some theoretical guidance for its application in EC treatment.
食品添加剂柠檬酸对人食管癌EC109细胞生长的影响
目的食管癌已成为中国最常见的肿瘤类型之一。因此,迫切需要新的药物和治疗策略来提高EC患者的术后生存率。作为一种食品添加剂,多项证据表明柠檬酸可以作为糖酵解抑制剂来抑制某些肿瘤细胞的生长。然而,这种有机酸对人食管癌细胞株EC109生长的影响尚不清楚。材料与方法本实验采用MTT法测定细胞增殖率。荧光显微镜下采用Hoechst 33258染色观察细胞凋亡形态学变化。流式细胞术检测细胞凋亡率和线粒体膜电位(MMP)。采用乳酸脱氢酶(LDH)测定试剂盒测定柠檬酸对细胞膜通透性的影响。结果与对照组相比,较高柠檬酸浓度(800、1600 μg/ml)处理后,细胞增殖能力明显降低。柠檬酸处理后EC109细胞出现典型的凋亡形态,如染色质凝集和凋亡小体的出现。400 ~ 1600 μg/ml柠檬酸处理后,细胞凋亡指标显著升高(P<0.01)。各治疗组细胞外LDH活性和MMP损失均显著高于对照组(P<0.05),且呈剂量依赖性。结论柠檬酸通过抑制EC109细胞增殖和诱导细胞凋亡来抑制EC109细胞的生长,可能为其在EC治疗中的应用提供一定的理论指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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