交易激励
木犀草素
PI3K/AKT/mTOR通路
癌症研究
基因敲除
蛋白激酶B
癌细胞
化学
槲皮素
细胞培养
生物
分子生物学
癌症
信号转导
生物化学
转录因子
基因
遗传学
抗氧化剂
作者
Ku‐Chung Chen,Wen-Hsien Hsu,Jhih-Yun Ho,Cheng-Wei Lin,Cheng-Ying Chu,Chithan Kandaswami,Ming-Ting Lee,Chia‐Hsiung Cheng
出处
期刊:Journal of Food and Drug Analysis
[The Journal of Food and Drug Analysis (JFDA), Food and Drug Administration, Taiwan (TFDA)]
日期:2018-02-13
卷期号:26 (3): 1180-1191
被引量:60
标识
DOI:10.1016/j.jfda.2018.01.012
摘要
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.
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