dc.contributor.author | Abtin, M | |
dc.contributor.author | Alivand, MR | |
dc.contributor.author | Khaniani, MS | |
dc.contributor.author | Bastami, M | |
dc.contributor.author | Zaeifizadeh, M | |
dc.contributor.author | Derakhshan, SM | |
dc.date.accessioned | 2018-08-26T04:52:51Z | |
dc.date.available | 2018-08-26T04:52:51Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/37717 | |
dc.description.abstract | Breast cancer (BC) is the leading cause of cancer mortality in women worldwide. It recently was proven that miRNAs play a critical role in BC development. The use of natural agents for control of cancer by modulating miRNAs is promising. Oleuropein is a natural polyphenolic agent with anti-neoplastic properties and is well tolerated by humans. This study was undertaken to determine the therapeutic effects of oleuropein through modulation of master oncomiRs (miR-21 and miR-155) in BC cells. The present study provides the first link between miRNA and oleuropein as a mechanism in BC. MCF-7 cells were tested with and without oleuropein and the cell viability, apoptosis, and migration were examined. The effect of oleuropein on miR-21 and miR-155 expression was assessed through qRT-PCR. It was found that oleuropein induced apoptosis and retarded cell migration and invasion in a dose-dependent manner in the human MCF7 BC cell line. It was observed that oleuropein significantly decreased expression of both miR-21 and miR-155 over time in a dose-dependent manner. These results demonstrate that oleuropein is a potential therapeutic and preventive agent for BC. Oleuropein exhibits an anti-cancer effect by modulation of tumor suppressor gene expression, which is targeted by oncomiRs. | |
dc.language.iso | English | |
dc.relation.ispartof | Journal of cellular biochemistry | |
dc.title | Simultaneous downregulation of miR-21 and miR-155 through oleuropein for breast cancer prevention and therapy. | |
dc.type | article | |
dc.citation.index | Pubmed | |
dc.identifier.DOI | https://doi.org/10.1002/jcb.26754 | |