Ozen Mustafa, Karatas Omer Faruk, Gulluoglu Sukru, Bayrak Omer Faruk, Sevli Serhat, Guzel Esra, Ekici Isin D, Caskurlu Turhan, Solak Mustafa, Creighton Chad J, Ittmann Michael
1Department of Medical Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Cancer Invest. 2015 Jul;33(6):251-8. doi: 10.3109/07357907.2015.1025407. Epub 2015 May 7.
We aimed to perform functional analysis of miR-145-5p in prostate cancer (PCa) cells and to identify targets of miR-145-5p for understanding its role in PCa pathogenesis. PC3, DU145, LNCaP PCa, and PNT1a nontumorigenic prostate cell lines were utilized for functional analysis of miR-145-5p. Its overexpression caused inhibition of proliferation through apoptosis and reduced migration in PCa cells. SOX2 expression was significantly decreased in both mRNA and protein level in miR-145-5p-overexpressed PCa cells. We proposed that miR-145-5p, being an important regulator of SOX2, carries a crucial role in PCa tumorigenesis.
我们旨在对前列腺癌细胞中的miR-145-5p进行功能分析,并确定miR-145-5p的靶标,以了解其在前列腺癌发病机制中的作用。利用PC3、DU145、LNCaP前列腺癌细胞系和PNT1a非致瘤性前列腺细胞系对miR-145-5p进行功能分析。其过表达通过诱导凋亡抑制前列腺癌细胞增殖,并降低细胞迁移能力。在miR-145-5p过表达的前列腺癌细胞中,SOX2的mRNA和蛋白水平均显著降低。我们认为,miR-145-5p作为SOX2的重要调节因子,在前列腺癌的肿瘤发生过程中起着关键作用。