Chen Xiaoguang, Lv Qiongxia, Liu Yumei, Deng Wen
Animal Science and Technology School, Henan University of Science and Technology, Luoyang, China.
Cell J. 2017 Winter;18(4):493-502. doi: 10.22074/cellj.2016.4716. Epub 2016 Sep 26.
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.
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.
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.
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.
如今,食管癌已成为中国最常见的癌症类型之一。因此,迫切需要新的药物和治疗策略来提高食管癌患者的术后生存率。作为一种食品添加剂,已有多项证据表明柠檬酸可作为糖酵解抑制剂来抑制某些肿瘤细胞的生长。然而,关于这种有机酸对人食管癌细胞系EC109生长的影响却知之甚少。
在本实验研究中,使用MTT法测定细胞增殖率。采用Hoechst 33258染色,通过荧光显微镜评估细胞凋亡的形态变化。使用流式细胞术检测细胞凋亡率和线粒体膜电位(MMP)。使用乳酸脱氢酶(LDH)检测试剂盒,通过测量LDH活性来评估柠檬酸对细胞膜通透性的影响。
与对照组相比,当细胞用较高浓度的柠檬酸(800、1600μg/ml)处理时,细胞增殖明显降低。用柠檬酸处理后观察到EC109细胞典型的凋亡形态,如染色质浓缩和凋亡小体的出现。用400 - 1600μg/ml浓度的柠檬酸处理后,细胞凋亡指数显著增加(P<0.01)。所有处理组的细胞外LDH活性和MMP的丧失均显著高于对照组(P<0.05),且呈剂量依赖性。
这些结果表明,柠檬酸通过抑制细胞增殖和诱导凋亡来阻止EC109细胞生长,这可能为其在食管癌治疗中的应用提供一些理论指导。