Department of Traditional Chinese Medicine, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Biochem Biophys Res Commun. 2012 Sep 21;426(2):247-52. doi: 10.1016/j.bbrc.2012.08.075. Epub 2012 Aug 23.
MicroRNAs (miRNAs) have crucial roles in the development and progression of human cancers, including hepatocellular carcinoma (HCC). Recent studies have shown that microRNA-124 (miR-124) was downregulated in HCC; however, the underlying mechanisms by which miR-124 suppresses tumorigenesis in HCC are largely unknown. In this study, we report that phosphoinositide 3-kinase catalytic subunit alpha (PIK3CA) is a novel target of miR-124 in HepG2 cells. Overexpression of miR-124 resulted in decreased expression of PIK3CA at both mRNA and protein levels. We found that miR-124 overexpression markedly suppressed cell proliferation by inducing G1-phase cell-cycle arrest in vitro. Consistent with the restoring miR-124 expression, PIK3CA knockdown suppressed cell proliferation, whereas overexpression of PIK3CA abolished the suppressive effect of miR-124. Mechanistic studies showed that miR-124-mediated reduction of PIK3CA resulted in suppression of PI3K/Akt pathway. The expressions of Akt and mTOR, key components of the PI3K/Akt pathway, were all downregulated. Moreover, we found overexpressed miR-124 effectively repressed tumor growth in xenograft animal experiments. Taken together, our results demonstrate that miR-124 functions as a growth-suppressive miRNA and plays an important role in inhibiting the tumorigenesis through targeting PIK3CA.
微小 RNA(miRNAs)在人类癌症的发展和进展中起着至关重要的作用,包括肝细胞癌(HCC)。最近的研究表明,微小 RNA-124(miR-124)在 HCC 中下调;然而,miR-124 抑制 HCC 肿瘤发生的潜在机制在很大程度上尚不清楚。在这项研究中,我们报告说,磷酸肌醇 3-激酶催化亚基 α(PIK3CA)是 HepG2 细胞中 miR-124 的一个新靶点。miR-124 的过表达导致 PIK3CA 在 mRNA 和蛋白水平上的表达降低。我们发现 miR-124 过表达通过体外诱导 G1 期细胞周期停滞显著抑制细胞增殖。与恢复 miR-124 表达一致,PIK3CA 敲低抑制细胞增殖,而 PIK3CA 的过表达则消除了 miR-124 的抑制作用。机制研究表明,miR-124 介导的 PIK3CA 减少导致 PI3K/Akt 途径的抑制。Akt 和 mTOR 的表达,PI3K/Akt 途径的关键组成部分,均下调。此外,我们发现过表达的 miR-124 在异种移植动物实验中有效地抑制了肿瘤生长。总之,我们的研究结果表明,miR-124 作为一种生长抑制性 miRNA 发挥作用,通过靶向 PIK3CA 在抑制肿瘤发生中发挥重要作用。