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Enhanced Anti-tumor Activity by the Combination of the Natural Compounds (−)-Epigallocatechin-3-gallate and Luteolin: POTENTIAL ROLE OF p53*

机译:通过天然化合​​物(-)-表没食子儿茶素-3-没食子酸酯和木犀草素的组合增强的抗肿瘤活性:p53的潜在作用*

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摘要

Natural dietary agents have drawn a great deal of attention toward cancer prevention because of their wide safety margin. However, single agent intervention has failed to bring the expected outcome in clinical trials; therefore, combinations of chemopreventive agents are gaining increasingly popularity. In the present study, we investigated a combinatorial approach using two natural dietary polyphenols, luteolin and EGCG, and found that their combination at low doses (at which single agents induce minimal apoptosis) synergistically increased apoptosis (3–5-fold more than the additive level of apoptosis) in both head and neck and lung cancer cell lines. This combination also significantly inhibited growth of xenografted tumors in nude mice. The in vivo findings also were supported by significant inhibition of Ki-67 expression and increase in TUNEL-positive cells in xenografted tissues. Mechanistic studies revealed that the combination induced mitochondria-dependent apoptosis in some cell lines and mitochondria-independent apoptosis in others. Moreover, we found more efficient stabilization and ATM-dependent Ser15 phosphorylation of p53 due to DNA damage by the combination, and ablation of p53 using shRNA strongly inhibited apoptosis as evidenced by decreased poly(ADP-ribose) polymerase and caspase-3 cleavage. In addition, we observed mitochondrial translocation of p53 after treatment with luteolin or the combination of EGCG and luteolin. Taken together, our results for the first time suggest that the combination of luteolin and EGCG has synergistic/additive growth inhibitory effects and provides an important rationale for future chemoprevention trials of head and neck and lung cancers.
机译:天然饮食剂因其广泛的安全性而在癌症预防方面引起了极大的关注。但是,单药干预未能在临床试验中带来预期的结果。因此,化学预防剂的组合越来越受欢迎。在本研究中,我们研究了使用两种天然饮食多酚,木犀草素和EGCG的组合方法,并发现它们在低剂量时(单药诱导最小凋亡)的组合协同增加了凋亡(比添加剂多3-5倍)头颈部和肺癌细胞系的凋亡水平)。这种组合还显着抑制了裸鼠中异种移植肿瘤的生长。体内发现也得到了Ki-67表达的显着抑制和异种移植组织中TUNEL阳性细胞增加的支持。机理研究表明,该组合在某些细胞系中诱导线粒体依赖性凋亡,而在另一些细胞系中诱导线粒体非依赖性凋亡。此外,我们发现由于组合的DNA损伤,p53可以更有效地稳定化和依赖ATM的Ser15磷酸化,并且使用shRNA消融p53可以强烈抑制细胞凋亡,如聚(ADP-核糖)聚合酶和caspase-3裂解的减少所证明。另外,我们观察到在用木犀草素或EGCG和木犀草素的组合治疗后p53的线粒体易位。两者合计,我们的结果首次表明,木犀草素和EGCG的组合具有协同/加性生长抑制作用,并为未来头颈和肺癌的化学预防试验提供了重要的依据。

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