Simultaneous downregulation of miR-21 and miR-155 through oleuropein for breast cancer prevention and therapy

被引:48
作者
Abtin, Maryam [1 ,2 ]
Alivand, Mohammad R. [2 ]
Khaniani, Mahmoud S. [2 ]
Bastami, Milad [2 ]
Zaeifizadeh, Mohammad [3 ]
Derakhshan, Sima M. [1 ,2 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Med, Dept Med Genet, Tabriz, Iran
[3] Islamic Azad Univ, Dept Genet, Ardabil Branch, Ardebil, Iran
关键词
anti-cancer effect; breast cancer; miRNA; miR-21; miR-155; oleuropein; EPITHELIAL-MESENCHYMAL TRANSITION; LYMPH-NODE METASTASIS; TUMOR-SUPPRESSOR; MICRORNA-21; TARGETS; UP-REGULATION; STEM-CELLS; PATHWAY; EXPRESSION; APOPTOSIS; GROWTH;
D O I
10.1002/jcb.26754
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:7151 / 7165
页数:15
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