Department of Biochemistry and Molecular Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
J Food Drug Anal. 2018 Jul;26(3):1180-1191. doi: 10.1016/j.jfda.2018.01.012. Epub 2018 Feb 13.
Flavonoids luteolin and quercetin can inhibit growth and metastasis of cancer cells. In our previous report, luteolin and quercetin was shown to block Akt/mTOR/c-Myc signaling. Here, we found luteolin and quercetin reduced protein level and transactivation activity of RPS19 in A431-III cells, which is isolated from parental A431 (A431-P) cell line. Further investigation the inhibitory mechanism of luteolin and quercetin on RPS19, we found c-Myc binding sites on RPS19 promoter. The Akt inhibitor LY294002, mTOR inhibitor rapamycin and c-Myc inhibitor 10058-F4 significantly suppressed RPS19 expression and transactivation activities. Overexpression and knockdown of c-Myc in cancer cells show RPS19 expression was regulated by c-Myc. Furthermore, Knockdown and overexpression of RPS19 was used to analyze of the function of RPS19 in cancer cells. The epithelial-mesenchymal transition (EMT) markers and metastasis abilities of cancer cells were also regulated by RPS19. These data suggest that luteolin and quercetin might inhibit metastasis of cancer cells by blocking Akt/mTOR/c-Myc signaling pathway to suppress RPS19-activated EMT signaling.
类黄酮木犀草素和槲皮素可以抑制癌细胞的生长和转移。在我们之前的报告中,木犀草素和槲皮素被证明可以阻断 Akt/mTOR/c-Myc 信号通路。在这里,我们发现木犀草素和槲皮素可以降低 A431-III 细胞(从亲本 A431(A431-P)细胞系中分离出来)中 RPS19 的蛋白水平和转录激活活性。进一步研究木犀草素和槲皮素对 RPS19 的抑制机制,我们发现 RPS19 启动子上有 c-Myc 结合位点。Akt 抑制剂 LY294002、mTOR 抑制剂 rapamycin 和 c-Myc 抑制剂 10058-F4 显著抑制 RPS19 的表达和转录激活活性。在癌细胞中过表达和敲低 c-Myc 表明 c-Myc 调节 RPS19 的表达。此外,敲低和过表达 RPS19 用于分析 RPS19 在癌细胞中的功能。上皮-间充质转化 (EMT) 标志物和癌细胞的转移能力也受到 RPS19 的调节。这些数据表明,木犀草素和槲皮素可能通过阻断 Akt/mTOR/c-Myc 信号通路抑制 RPS19 激活的 EMT 信号来抑制癌细胞的转移。