首页> 外文期刊>The Journal of Nutritional Biochemistry >Enhanced inhibition of prostate cancer xenograft tumor growth by combining quercetin and green tea.
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Enhanced inhibition of prostate cancer xenograft tumor growth by combining quercetin and green tea.

机译:通过结合槲皮素和绿茶增强对前列腺癌异种移植肿瘤生长的抑制。

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The chemopreventive activity of green tea (GT) is limited by the low bioavailability and extensive methylation of GT polyphenols (GTPs) in vivo. We determined whether a methylation inhibitor quercetin (Q) will enhance the chemoprevention of prostate cancer in vivo. Androgen-sensitive LAPC-4 prostate cancer cells were injected subcutaneously into severe combined immunodeficiency (SCID) mice one week before the intervention. The concentration of GTPs in brewed tea administered as drinking water was 0.07% and Q was supplemented in diet at 0.2% or 0.4%. After 6-weeks of intervention tumor growth was inhibited by 3% (0.2% Q), 15% (0.4% Q), 21% (GT), 28% (GT+0.2% Q) and 45% (GT+0.4% Q) compared to control. The concentration of non-methylated GTPs was significantly increased in tumor tissue with GT+0.4% Q treatment compared to GT alone, and was associated with a decreased protein expression of catechol-O-methyltransferase and multidrug resistance-associated protein (MRP)-1. The combination treatment was also associated with a significant increase in the inhibition of proliferation, androgen receptor and phosphatidylinositol 3-kinase/Akt signaling, and stimulation of apoptosis. The combined effect of GT+0.4% Q on tumor inhibition was further confirmed in another experiment where the intervention started prior to tumor inoculation. These results provide a novel regimen by combining GT and Q to improve chemoprevention in a non-toxic manner and warrant future studies in humans.
机译:绿茶(GT)的化学预防活性受到体内生物利用度低和GT多酚(GTP)广泛甲基化的限制。我们确定了甲基化抑制剂槲皮素(Q)是否会增强体内前列腺癌的化学预防作用。干预前一周,将对雄激素敏感的LAPC-4前列腺癌细胞皮下注射入严重的联合免疫缺陷(SCID)小鼠中。饮用的冲泡茶中GTP的浓度为0.07%,饮食中补充Q的含量为0.2%或0.4%。干预6周后,肿瘤的生长被抑制了3%(0.2%Q),15%(0.4%Q),21%(GT),28%(GT + 0.2%Q)和45%(GT + 0.4%)问)与对照相比。与单独使用GT相比,GT + 0.4%Q处理的肿瘤组织中非甲基化GTP的浓度显着增加,并且与儿茶酚-O-甲基转移酶和多药耐药相关蛋白(MRP)-1的蛋白表达降低有关。联合治疗还与增殖抑制,雄激素受体和磷脂酰肌醇3-激酶/ Akt信号转导的显着增加以及细胞凋亡的刺激有关。 GT + 0.4%Q对肿瘤抑制的综合作用在另一个实验中得到了进一步证实,该实验在接种肿瘤之前开始。这些结果通过结合GT和Q提供了一种新颖的方案,以无毒的方式改善了化学预防的效果,值得在人类中进行进一步的研究。

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