期刊
JOURNAL OF CELLULAR PHYSIOLOGY
卷 234, 期 10, 页码 17876-17885出版社
WILEY
DOI: 10.1002/jcp.28418
关键词
crocin; epithelial-mesenchymal transition; gastric cancer; metastasis; miR-320; KLF5; HIF-1 alpha
资金
- Shanghai Pudong Commission of Health and Family Planning [PWRd2016-12]
- National Natural Science Foundation of China [81503541]
- Talents Training Program of Seventh People's Hospital of Shanghai University of TCM [BDX2016-01]
The biological activities of crocin, one of the main bioactive compounds of saffron, include anti-inflammatory, antioxidant, antidepressant, and anticancer effects. Crocin has been shown to trigger the apoptosis of gastric cancer cells, but its effect on the metastasis of gastric cancer cells remains unclear. Kruppel-like factor 5 (KLF5) and hypoxia-inducible factor-1 alpha (HIF-1 alpha) are important transcription factors in the development of gastric cancer. KLF5 and HIF-1 alpha expression were analyzed in gastric cancer tissues and cells. Following exposure to crocin, AGS and HGC-27 gastric cancer cells were assessed with regard to migration, invasion, and epithelial-mesenchymal transition (EMT) as well as the expression of KLF5, HIF-1 alpha, and microRNA-320 (miR-320). The miR-320/KLF5/HIF-1 alpha signaling pathway became the focus for further investigation of the mechanism of crocin in gastric cancer cell migration, invasion, and EMT. KLF5 and HIF-1 alpha expression were elevated in gastric cancer tissues and cells, and KLF5 expression was positively correlated with the HIF-1 alpha level in gastric cancer tissues. Crocin was associated with reduced expression of KLF5 and HIF-1 alpha, whereas miR-320 expression was increased. Crocin also inhibited the migration, invasion, and EMT of gastric cancer cells. Upregulation of KLF5 attenuated crocin's function and elevated HIF-1 alpha expression. Dual-luciferase reporter assay demonstrated that KLF5 was a target gene of miR-320. Crocin modulated KLF5 expression via elevation of miR-320 expression. In conclusion, crocin inhibits the EMT, migration, and invasion of gastric cancer cells, and this activity is mediated through miR-320/KLF5/HIF-1 alpha signaling.
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