Department of Orthopedics, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, P.R. China.
Department of Pathology, Cancer Hospital of Jiangxi Province, Nanchang, Jiangxi, P.R. China.
Int J Mol Med. 2014 Mar;33(3):633-9. doi: 10.3892/ijmm.2013.1602. Epub 2013 Dec 23.
The activation of PI3K/Akt and the overexpression of fatty acid synthase (FASN) are frequently observed in human osteosarcoma (OS). In the present study, in order to investigate the possible association between the phosphorylation of Akt and FASN expression, immunohistochemical staining was conducted on 24 OS specimens from patients with pulmonary metastasis, which revealed a significant positive correlation between phosphorylated Akt (p-Akt) and the expression of FASN (R=0.469, P=0.04). To investigate the association between p-Akt and FASN in vitro, human U2-OS OS cells were treated with FASN-specific RNAi plasmid or LY294002 (an inhibitor of PI3k/Akt). The mRNA levels of Akt and FASN were measured by real-time PCR. Western blot analysis was also performed to detect the protein experession of PI3K, Akt, p-Akt and FASN. The results demonstrated that the PI3K/Akt signaling pathway modulates FASN expression; the inhibition of FASN resulted in the downregulation of p-Akt in the U2-OS cells. Furthermore, the effects induced by the inhibition of the activity of p-Akt or FASN on the malignant phenotype of U2-OS cells were investigated, demonstrating that the malignant phenotype was inhibited by suppressing the activity of PI3K/Akt or FASN in the U2-OS cells. The findings from our study suggest the existence of a positive feedback regulation between Akt phosphorylation and FASN expression and that this loop may play an important role in the malignant phenotype of OS cells.
PI3K/Akt 的激活和脂肪酸合酶(FASN)的过度表达在人类骨肉瘤(OS)中经常观察到。在本研究中,为了研究 Akt 磷酸化与 FASN 表达之间可能存在的关联,对 24 例来自肺转移患者的 OS 标本进行了免疫组织化学染色,结果显示磷酸化 Akt(p-Akt)与 FASN 的表达之间存在显著正相关(R=0.469,P=0.04)。为了研究体外 p-Akt 和 FASN 之间的关联,用人 U2-OS OS 细胞用 FASN 特异性 RNAi 质粒或 LY294002(PI3K/Akt 的抑制剂)处理。通过实时 PCR 测量 Akt 和 FASN 的 mRNA 水平。还进行了 Western blot 分析以检测 PI3K、Akt、p-Akt 和 FASN 的蛋白表达。结果表明,PI3K/Akt 信号通路调节 FASN 表达;抑制 FASN 导致 U2-OS 细胞中 p-Akt 的下调。此外,还研究了抑制 p-Akt 或 FASN 的活性对 U2-OS 细胞恶性表型的影响,结果表明通过抑制 U2-OS 细胞中 PI3K/Akt 或 FASN 的活性抑制了恶性表型。我们的研究结果表明 Akt 磷酸化与 FASN 表达之间存在正反馈调节,该环路可能在 OS 细胞的恶性表型中发挥重要作用。