dc.contributor.author | Zununi Vahed, S | |
dc.contributor.author | Barzegari, A | |
dc.contributor.author | Rahbar Saadat, Y | |
dc.contributor.author | Goreyshi, A | |
dc.contributor.author | Omidi, Y | |
dc.date.accessioned | 2018-08-26T08:59:59Z | |
dc.date.available | 2018-08-26T08:59:59Z | |
dc.date.issued | 2017 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54865 | |
dc.description.abstract | Promising results from different studies on the effect of probiotics in cancer prevention and therapy have so far been reported. However, the molecular mechanism of the interaction of probiotics with cancer cells is yet to be fully understood. In the present study, Leuconostoc mesenteroides was isolated from traditional dairy products, and its probiotic characteristics were determined. HT-29 cells were treated with conditioned-medium of designated bacteria and the cell apoptosis was studied at cellular and molecular level using DAPI staining, flow cytometry, DNA ladder assays, and real-time quantitative-PCR (q-PCR). Based on our findings, L. mesenteroides promoted apoptosis in colon cancer cell line by upregulation of MAPK1, Bax, and caspase 3, and downregulation of AKT, NF-?B, Bcl-XL expressions and some key oncomicroRNAs such as miRNA-21 and miRNA-200b significantly (p ? 0.03). The results indicated the likelihood of the examined probiotic as an alternative or complementary treatment modality in signaling-targeted cancer therapy. é 2017 | |
dc.language.iso | English | |
dc.relation.ispartof | Biomedicine and Pharmacotherapy | |
dc.subject | caspase 3 | |
dc.subject | immunoglobulin enhancer binding protein | |
dc.subject | microRNA 200b | |
dc.subject | microRNA 21 | |
dc.subject | mitogen activated protein kinase | |
dc.subject | mitogen activated protein kinase 1 | |
dc.subject | phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase | |
dc.subject | probiotic agent | |
dc.subject | protein Bax | |
dc.subject | protein bcl xl | |
dc.subject | protein kinase B | |
dc.subject | antineoplastic agent | |
dc.subject | apoptosis regulatory protein | |
dc.subject | caspase 3 | |
dc.subject | immunoglobulin enhancer binding protein | |
dc.subject | microRNA | |
dc.subject | mitogen activated protein kinase | |
dc.subject | phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase | |
dc.subject | protein kinase B | |
dc.subject | PTEN protein, human | |
dc.subject | antiinflammatory activity | |
dc.subject | apoptosis | |
dc.subject | Article | |
dc.subject | cancer cell | |
dc.subject | cancer inhibition | |
dc.subject | cell survival | |
dc.subject | colon cancer | |
dc.subject | conditioned medium | |
dc.subject | controlled study | |
dc.subject | down regulation | |
dc.subject | flow cytometry | |
dc.subject | HT-29 cell line | |
dc.subject | Leuconostoc mesenteroides | |
dc.subject | nonhuman | |
dc.subject | priority journal | |
dc.subject | protein expression | |
dc.subject | real time polymerase chain reaction | |
dc.subject | upregulation | |
dc.subject | cell survival | |
dc.subject | colon tumor | |
dc.subject | drug effect | |
dc.subject | human | |
dc.subject | inflammation | |
dc.subject | Leuconostoc mesenteroides | |
dc.subject | metabolism | |
dc.subject | signal transduction | |
dc.subject | tumor cell line | |
dc.subject | Antineoplastic Agents | |
dc.subject | Apoptosis | |
dc.subject | Apoptosis Regulatory Proteins | |
dc.subject | Caspase 3 | |
dc.subject | Cell Line, Tumor | |
dc.subject | Cell Survival | |
dc.subject | Colonic Neoplasms | |
dc.subject | Down-Regulation | |
dc.subject | HT29 Cells | |
dc.subject | Humans | |
dc.subject | Inflammation | |
dc.subject | Leuconostoc mesenteroides | |
dc.subject | MicroRNAs | |
dc.subject | Mitogen-Activated Protein Kinases | |
dc.subject | NF-kappa B | |
dc.subject | Proto-Oncogene Proteins c-akt | |
dc.subject | PTEN Phosphohydrolase | |
dc.subject | Signal Transduction | |
dc.subject | Up-Regulation | |
dc.title | Leuconostoc mesenteroides-derived anticancer pharmaceuticals hinder inflammation and cell survival in colon cancer cells by modulating NF-?B/AKT/PTEN/MAPK pathways | |
dc.type | Article | |
dc.citation.volume | 94 | |
dc.citation.spage | 1094 | |
dc.citation.epage | 1100 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.1016/j.biopha.2017.08.033 | |