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microRNA-372 inhibits proliferation and induces apoptosis in human breast cancer cells by directly targeting E2F1

Breast cancer is the most prevalent cancer and the leading cause of cancer-associated mortalities among women worldwide today. Accumulating evidence suggested that miR-372 may serve important roles in the initiation and development of various human cancers. However, the role of miR-372 in breast can...

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Detalles Bibliográficos
Autores principales: Zhao, Ya-Xin, Liu, Hua-Cheng, Ying, Wei-Yang, Wang, Cheng-Yu, Yu, Yao-Jun, Sun, Wei-Jian, Liu, Jie-Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779890/
https://www.ncbi.nlm.nih.gov/pubmed/28944922
http://dx.doi.org/10.3892/mmr.2017.7591
Descripción
Sumario:Breast cancer is the most prevalent cancer and the leading cause of cancer-associated mortalities among women worldwide today. Accumulating evidence suggested that miR-372 may serve important roles in the initiation and development of various human cancers. However, the role of miR-372 in breast cancer remains unknown. The present study demonstrated that the expression level of miR-372 in human breast cancer tissues and cell lines is significantly reduced compared with normal breast tissues cell lines. Furthermore, results of functional assays indicated that miR-372 inhibits cell proliferation and induces apoptosis in the MCF-7 human breast cancer cell line. E2F1 was identified as a direct functional target of miR-372 in breast cancer. In conclusion, the findings revealed that miR-372 may have the potential to act as a novel molecule for the diagnosis and therapy of patients with breast cancer.