Omnia Momtaz Al-Fakharany, A. Aziz, T. El-Banna, F. Sonbol
{"title":"粪肠球菌产肠蛋白e-342的免疫调节和抗癌活性","authors":"Omnia Momtaz Al-Fakharany, A. Aziz, T. El-Banna, F. Sonbol","doi":"10.4172/2155-9899.1000558","DOIUrl":null,"url":null,"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.","PeriodicalId":15473,"journal":{"name":"Journal of clinical & cellular immunology","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Immunomodulatory and Anticancer Activities of Enterocin Oe-342 Produced by Enterococcus Feacalis Isolated from Stool\",\"authors\":\"Omnia Momtaz Al-Fakharany, A. Aziz, T. El-Banna, F. Sonbol\",\"doi\":\"10.4172/2155-9899.1000558\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":15473,\"journal\":{\"name\":\"Journal of clinical & cellular immunology\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical & cellular immunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2155-9899.1000558\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical & cellular immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2155-9899.1000558","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Immunomodulatory and Anticancer Activities of Enterocin Oe-342 Produced by Enterococcus Feacalis Isolated from Stool
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.