Up-regulation of miR-۲۱ decreases chemotherapeutic effect of dendrosomal curcumin in breast cancer cells

  • سال انتشار: 1396
  • محل انتشار: مجله علوم پایه پزشکی ایران، دوره: 20، شماره: 4
  • کد COI اختصاصی: JR_IJBMS-20-4_002
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 237
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نویسندگان

Mohammad Javad Dehghan Esmatabadi

Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Baharak Farhangi

Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Maryam Montazeri

Department of Medical Biotechnology, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran

Hamideh Monfared

Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Roohollah Nakhaei Sistani

Department of Cellular Biotechnology, Faculty of Chemistry, Kashan University, Kashan, Iran

Majid Sadeghizadeh

Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

چکیده

Objective(s): Despite the good results of anticancer activities by curcumin, there are some hurdles that limit the use of curcumin as an anticancer agent. Many methods were examined to overcome this defect like the use of the dendrosomal curcumin (DNC). There is increasing evidence that miRNAs play important roles in biological processes. In this study, we focus on the roles of microRNA-۲۱ in the anti-cancer effects of DNC in breast cancer. Materials and Methods: Also, we have used different methods such as MTT, apoptosis, cell cycle analysis, transwell migration assay and RT-PCR to find out more. Results: We observed that miR-۲۱ decreased apoptotic cells in both cells (from ۶.۳۵% to ۰.۳۴ % and from ۷.۷۲% to ۱.۳۲% orderly) and DNC increased it. As well as, our findings indicated that cell migration capacity was increased by miR-۲۱ over expression and was decreased by DNC. The combination of miR-۲۱ vector transfection and DNC treatment showed lower percentage of apoptotic cells or a higher level of penetration through the membrane compared with DNC treatment alone. Furthermore, DNC induced a marked increase in the number of cells in sub G۱/G۱ phase and a decrease in G۲/M phase of the cell cycle in both; but, we observed reverse results compared it, after transfection with miR-۲۱ vector. Conclusion: We observed that miR-۲۱ suppress many aspects of anti-cancer effects of DNC in breast cancer cells, it seems that co-treatment with DNC and mir-۲۱ down-regulation may provide a clinically useful tool for drug-resistance breast cancer cells.

کلیدواژه ها

Breast Cancer, Cell cycle, Cell Proliferation, Curcumin, Dendrosomal curcumin, MicroRNA-۲۱

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