28 اردیبهشت 1403
زهره جهان افروز

زهره جهان افروز

مرتبه علمی: استادیار
نشانی: گروه زیست شناسی دانشگاه مراغه
تحصیلات: دکترای تخصصی / زیست شناسی- علوم سلولی مولکولی
تلفن: 04137278001-523
دانشکده: دانشکده علوم پایه

مشخصات پژوهش

عنوان
Effects of miR-21 downregulation and silibinin treatment in breast cancer cell lines
نوع پژوهش مقاله چاپ شده
کلیدواژه‌ها
Anti-miR-21; Apoptosis; Breast Cancer; MiR-21 mimic, Silibinin; PTEN
سال
2017
مجله CYTOTECHNOLOGY
شناسه DOI doi:10.1007/s10616-017-0076-5)
پژوهشگران زهره جهان افروز ، نسرین معتمد ، بهناز بخشنده

چکیده

Silibinin is a natural polyphenol with high antioxidant and anticancer properties, which causes cell cycle arrest and apoptosis in most cancer cell types including breast cancer, but the in-line mechanisms, are still unknown. Silibinin significantly downregulated oncomiR miR-21 expression in breast cancer cells. Here the effect of anti-miR-21 on cell viability, apoptotic induction, cell cycle distribution, and the expression levels of downstream targets of miR-21 were investigated in MCF-7 and T47D cells. MiR-21 mimic transfection was also applied in silibinin treated samples to evaluate functional role of miR-21downregulation on silibinin effects. It was found that after anti-miR-21 transfection, no significant changes were detected in cell viability, apoptosis (except early apoptosis), and cell cycle in MCF-7 and T47D cells. Compared to silibinin, miR-21 mimic transfection in combination with silibinin caused a slight modulation in some of the examined silibinin effects including apoptosis, Bcl2 mRNA and PTEN mRNA and protein levels. Silibinin slightly changed luciferase activity from reporters containing the miR-21 recognition elements from PTEN-3ʹUTR and Bcl2-3ʹUTR in both cell lines. Together these data demonstrated negligible cancer-progression impact of miR-21 and limited roles of miR-21 downregulation in examined silibinin effects, and strengthened the anti-cancer pathways of silibinin other than miR-21downregulation in MCF-7 and T47D cells.