下调和上调
小RNA
蛋白激酶B
细胞周期
癌症研究
信号转导
癌基因
细胞生长
MAPK/ERK通路
PI3K/AKT/mTOR通路
生物
细胞生物学
细胞
胰腺癌
激酶
癌症
生物化学
遗传学
基因
作者
Jian Zhou,Shiduo Song,Songbing He,Xinguo Zhu,Yi Zhang,Bin Yi,Bing Zhang,Gongzhao Qin,Dechun Li
标识
DOI:10.3892/ijmm.2014.1638
摘要
MicroRNAs (miRNAs or miRs) are believed to have great potential for use as molecular targets in the diagnosis and treatment of cancer. In this study, we demonstrate that miR-375 is downregulated in pancreatic carcinoma (PC) tissues and PC cell lines. We found that miR-375 negatively regulates the expression of 3-phosphoinositide-dependent protein kinase 1 (PDK1) by directly targeting the 3'UTR of the PDK1 transcript. To investigate the biological roles and the potential mechanisms of action of miR‑375, we induced either the up- or downregulation of miR-375 expression by transfecting various PC cells with miR-375 mimics or an inhibitor. Our results revealed that the upregulation of miR-375 inhibited cell growth and induced cell apoptosis, while the downregulation of miR-375 with the inhibitor had the opposite effect. In addition, our data demonstrate that miR-375 suppresses the malignant behavior of PC cells through the Akt signaling pathway rather than mitogen-activated protein kinase (MAPK) signaling pathways. Taken together, our findings indicate that targeting miR-375 by a genetic approach may provide a novel strategy for the treatment of PC.
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