Siroos Tarighi - Department of Cellular and molecular biology, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
Maryam Montazeri - Department of Medical Biotechnology, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
Fatemeh Rohollah - Department of Cellular and molecular biology, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran

Background: Breast cancer is one of the common malignancies in women, for which doxorubicin (DOX) is widely used in its chemotherapy. Recently, it has been found that DOX affects the expression profile of oncogene genes and miRNAs. In this study, the impacts of DOX on the expressions of the STAT۳ gene, miR-۸۷۴-۳p, and miR-۳۳۷-۳p were studied in the MCF-۷ breast cancer cell line. Methods: After exposure of MCF-۷ cells with DOX, the MTT method was applied for evaluating the cell viability. Apoptosis and necrosis percentages were measured using flow cytometry. Also, the levels of ROS and NF-κB were measured in DOX-treated cells. Then, exosomes secreted from these cells were prepared. The shape of exosomes was studied by SEM. Finally, the expression of bax, bcl-۲, p۵۳, casp۳, STAT۳ gene, and miR-۸۷۴-۳p and miR-۳۳۷-۳p in MCF-۷ cells as well as exosomes were evaluated using the RT-PCR technique. Data analysis was done by T-test in GraphPad Prism۸ software. Results: The exposure of MCF-۷ cells to doxorubicin led to a concentration-dependent decrease in cell viability and increases in apoptosis and necrosis. ROS and NF-κB activity were increased in DOX-treated cells. In DOX-treated cells, decreased expressions of bcl-۲ and STAT۳ genes and overexpression of bax, p۵۳, casp۳, miR-۸۷۴-۳p, and miR-۳۳۷-۳p were observed compared to untreated control cells. Conclusion: One of the mechanisms of the anti-breast cancer effects of DOX is the induction of changes in the expression of oncogenic genes, mediating by downregulating of STAT۳ gene and overexpressing miR-۸۷۴-۳p and miR-۳۳۷-۳p. More studies are needed in this field.

Breast cancer, Gene, miRNA, Doxorubicin