Genistein inhibits the growth and regulates the migration and invasion abilities of melanoma cells via the FAK/paxillin and MAPK pathways

被引:83
作者
Cui, Shuna [1 ,2 ,3 ]
Wang, Juan [1 ]
Wu, Qingqing [1 ]
Qian, Jing [1 ,2 ]
Yang, Changshui [1 ]
Bo, Ping [1 ]
机构
[1] Yangzhou Univ, Coll Med, Jiangsu Key Lab Integrated Tradit Chinese & Weste, Yangzhou, Jiangsu, Peoples R China
[2] Yangzhou Univ, Affiliated Hosp, Dept Obstet & Gynaecol, Yangzhou, Jiangsu, Peoples R China
[3] Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
genistein; melanoma cells; invasion and migration; FAK/paxillin pathway; MAPK pathway; FOCAL ADHESION KINASE; MATRIX-METALLOPROTEINASE TYPE-2; CANCER CELLS; SIGNALING PATHWAYS; PANCREATIC-CANCER; TYROSINE PHOSPHORYLATION; MALIGNANT-MELANOMA; TUMOR PROGRESSION; REPRESSOR SNAIL; GASTRIC-CANCER;
D O I
10.18632/oncotarget.15535
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genistein is one of the main components of soy-based foods, which are widely known for the ir many benefits, including anti-cancer, anti-inflammatory, and antioxidant effects. In this study, we investigated the anti-metastasis effects of genistein on B16F10 melanoma cells. Our results showed that genistein strongly inhibited B16F10 cell proliferation and induced apoptosis in time-and concentration-dependent manners. Genistein altered the morphology of B16F10 cells to an elongated shape with slim pseudopodia-like protrusions. Moreover, genistein inhibited the invasion and migration abilities of B16F10 cells in a dose-dependent manner. On one hand, a high concentration of genistein (100 mu M) significantly inhibited cell adhesion and migration, as shown by wound healing assays and transwell-migration and invasion assays. Furthermore, the expression levels of p-FAK, p-paxillin, tensin-2, vinculin, and a-actinin were decreased by genistein. As a result, genistein is believed to strongly downregulate the migration and invasion abilities of B16F10 cells via the FAK/paxillin pathway. Moreover, p-p38, p-ERK, and p-JNK levels were also dramatically decreased by treatment with genistein. Finally, genistein significantly decreased the gene expression of FAK, paxillin, vimentin, and epithelial-to-mesenchymal transition-related transcription factor Snail, as shown by real-time PCR (qPCR) analysis. On the other hand, a lower concentration of genistein (12.5 mu M) significantly promoted both invasion and migration by activating the FAK/paxillin and MAPK signaling cascades. Taken together, this study showed for the first time that genistein exerts dual functional effects on melanoma cells. Our findings suggest that genistein regulates the FAK/paxillin and MAPK signaling pathways in a highly concentration-dependent manner. Patients with melanoma should therefore be cautious of consuming soy-based foods in their diets.
引用
收藏
页码:21674 / 21691
页数:18
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