Investigating the effects of miR-۱۳۸ replacement on inhibiting cell migration and induction of apoptosis in breast cancer cell line

Publish Year: 1399
نوع سند: مقاله کنفرانسی
زبان: English
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CIGS16_025

تاریخ نمایه سازی: 14 اردیبهشت 1400

Abstract:

Background and Aim: MicroRNAs (small noncoding RNAs of ۲۰-۲۴ nucleotides long) are involved in the regulation of post-transcriptional gene expression, have close links with various cancers. Of these, miR-۱۳۸ is a well-known microRNA with multiple tumor suppressor effects. In this study we investigated the effects of miR-۱۳۸ replacement on inhibiting cell migration and induction of apoptosis in breast cancer cell line.Methods: At first miR-۱۳۸ mimic was transfected into MAD-MB-۲۳۱ cells using electroporation method and optimum dose of miR-۱۳۸ was determinded by MTT assay. At next stages we evaluated the effects of miR-۱۳۸ mimic on cell migration and apoptosis using wound healing assay and Annexin V- FITC/PI kit (flowcytometry) respectively. All data was analyzed by Graph Pad Prism software.Results: The optimum dose of transfected miR-۱۳۸ mimic into MDA-MB-۲۳۱ cells was determinded in ۲۰ pMol/ul. The flowcytometery method demonstrated that transfected cells with miR-۱۳۸ mimic have significant apoptotic profiles in comparison with control cells and transfected cells with NC-miR-mimic. As well as, wound healing assay showed that miR-۱۳۸ mimic decreases the migration ability of cells.Conclusion: This study showed that miR-۱۳۸ is downregulated in MDA-MB-۲۳۱cells in comparison with control cells. Also the transfection of miR-۱۳۸ mimic into MDA-MB-۲۳۱ cells decreases cell migration and induces cell apoptosis.

Authors

Mina Rasoolnezhad

Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran

Reza Safaralizadeh

Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran

Behzad Baradaran

lmmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran