游离脂肪酸受体1
GPR120
生物
A549电池
基因敲除
受体
癌细胞
G蛋白偶联受体
游离脂肪酸受体
细胞生物学
细胞
生物化学
癌症研究
脂肪酸
癌症
细胞凋亡
兴奋剂
多不饱和脂肪酸
遗传学
作者
Tsubasa Kita,Yui Kadochi,Kazuhisa Takahashi,Kaori Fukushima,Eri Yamasaki,Taiki Uemoto,Miku Hirane,Nobuyuki Fukushima,Kanya Honoki,Toshifumi Tsujiuchi
标识
DOI:10.1016/j.yexcr.2016.03.008
摘要
Free fatty acids (FFAs) are dietary nutrients which mediate a variety of biological effects through binding to G-protein-coupled FFA receptors (FFARs). G-protein-coupled receptor 120 (GPR120) and GPR40 are identified as FFARs for long- and medium-chain fatty acids. Here we investigated whether GPR120 and GPR40 are involved in the acquisition of malignant properties in lung cancer cells. Three lung cancer RLCNR, LL/2 and A549 cells used in this study expressed GPR120 and GPR40 genes. The cell motile activities of all cells were significantly suppressed by a GPR40 antagonist GW1100. In addition, GPR40 knockdown inhibited the cell motile activity of A549 cells. In gelatin zymography, matrix metalloproteinase-2 (MMP-2) activity in GPR40 knockdown was significantly lower than that in control cells. Next, to evaluate effects of GPR120 and GPR40 on cellular functions induced by anti-cancer drug, the long-term cisplatin (CDDP) treated (A549-CDDP) cells were generated. The expression levels of GPR120 and GPR40 were significantly decreased in A549-CDDP cells. While A549-CDDP cells showed the high cell motile activity, GW1100 suppressed the cell motile activity of A549-CDDP cells. These results demonstrate that GPR120 negatively and GPR40 positively regulate cellular functions during tumor progression in lung cancer cells.
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