In vitro study on anti-cancer properties of genistein in tongue cancer

被引:11
|
作者
Ardito, Fatima [1 ]
Pellegrino, Mario R. [1 ]
Perrone, Donatella [1 ]
Troiano, Giuseppe [1 ]
Cocco, Armando [1 ]
Lo Muzio, Lorenzo [1 ]
机构
[1] Foggia Univ, Dept Clin & Expt Med, Via Rovelli 50, I-71122 Foggia, Italy
来源
ONCOTARGETS AND THERAPY | 2017年 / 10卷
关键词
genistein; tongue cancer; xCELLgence system; cell adhesion; cell proliferation; SQUAMOUS-CELL CARCINOMA; ORAL-CANCER; KINASE INHIBITORS; APOPTOSIS; PATHWAY; GROWTH; HEAD; 5-FLUOROURACIL; PROLIFERATION; INVASIVENESS;
D O I
10.2147/OTT.S133632
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Purpose: Tongue cancer is an extremely aggressive disease and is characterized by a poor prognosis. It is a complex disease to treat and current therapies have produced mediocre results with many side effects. Some facts suggest that natural essences can support traditional cancer therapy by carrying out a synergistic function with chemotherapy. Therefore, we evaluated the antitumor effects of genistein on tongue carcinoma cells. Methods: Genistein 20, 50 and 100 mu M were used for 24, 48 and 72 hours on 3 tongue carcinoma cell lines. xCELLigence system was used to evaluate the effects on cell adhesion, proliferation and to calculate IC50 values. Both MTT assay and Trypan blue assay were used to evaluate alterations in cell viability, scratch assay for cell migration and Western blot analysis for expression of some proteins. Results: Cell adhesion was inhibited especially between 20 and 50 mu M of genistein treatment. Proliferation was reduced by 50% for treatments with 20 mu M at 24 hours, with 20 or 50 mu M at 48 and 50 mu M at 72 hours (P<0.0001). Viability tests confirmed a proportional reduction in concentration of genistein and duration of treatments. Even cell migration was reduced significantly (P<0.001). Genistein down-regulates vitronectin, OCT4 and survivin. Conclusion: This in vitro study clarifies the anti-tumor effect of genistein on tongue carcinoma. In vivo studies are needed to confirm these data and develop a suitable delivery system that is capable of acting directly on tumor.
引用
收藏
页码:5405 / 5415
页数:11
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