Immunomodulatory and Anticancer Activities of Enterocin Oe-342 Produced by Enterococcus Feacalis Isolated from Stool

Omnia Momtaz Al-Fakharany, A. Aziz, T. El-Banna, F. Sonbol
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引用次数: 5

Abstract

Objectives: This study evaluated the anticancer activity of Entr. faecalis enterocin OE-342 by testing its direct antitumor effects on colorectal cancer cell line, as well as, its immunomodulatory effects. Methods: The anticancer potentiality of this enterocin against human colorectal adenocarcinoma (HCT-116) cells was evaluated using cytotoxicity, cell cycle analysis, apoptosis and monitoring morphological changes of the treated cells. Also the immunomodulatory effects of the tested enterocin were quantified on LPS-induced PBMCs cell model with monitoring TNF-α and IFNγ levels using flowcytometry. Results: The obtained data showed that enterocin OE342 inhibited HCT-116 cellular viability in a concentration dependant manner with somewhat high IC50 value recording 49.920 mg/ml. Upon HCT-116 treatment with this enterocin the appearance of undergoing apoptotic cells characterized by cellular rounding up, shrinkage and membrane blebbing was observed. Cytotoxicity of enterocin OE-342 was accompanied by cell cycle arrest in the G2/M phase (24.66%) accompanied with an increase in the ratio of the apoptotic cells in the preG1cell cycle phase. Also, this enterocin affected the generation of TNF-α and IFNγ from LPS-induced PBMCs cell resulting in inhibition of the first by 27.3% and induction of the second by 69.5% which suggest the immunomodulatory effects of the tested enterocin. Conclusion: Taken together, our results suggest the anticancer potentialities of enterocin OE-342 against human colon cancer cells represented through its effects on both apoptotic and inflammatory pathways.
粪肠球菌产肠蛋白e-342的免疫调节和抗癌活性
目的:评价enterr的抗癌活性。通过对大肠杆菌肠球菌素OE-342对结直肠癌细胞系的直接抗肿瘤作用以及免疫调节作用进行研究。方法:采用细胞毒性、细胞周期分析、细胞凋亡及形态学变化监测等方法评价该肠球菌素对人结直肠癌(HCT-116)细胞的抑癌作用。采用流式细胞术监测TNF-α和IFNγ水平,定量测定肠球菌素对lps诱导的PBMCs细胞模型的免疫调节作用。结果:肠球菌素OE342抑制HCT-116细胞活力呈浓度依赖性,IC50值较高,为49.920 mg/ml。用该肠肽治疗HCT-116后,观察到凋亡细胞的外观,其特征是细胞聚集,收缩和膜起泡。肠球菌素OE-342的细胞毒性表现为G2/M期细胞周期阻滞(24.66%),g1前细胞周期凋亡细胞比例增加。此外,该肠球蛋白影响lps诱导的PBMCs细胞TNF-α和IFNγ的产生,导致前者抑制27.3%,后者诱导69.5%,这表明所测试的肠球蛋白具有免疫调节作用。结论:综上所述,我们的研究结果表明肠球菌素OE-342对人结肠癌细胞的抗癌潜力通过其对凋亡和炎症途径的影响来表现。
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