The dietary bioflavonoid quercetin synergizes with epigallocathechin gallate (EGCG) to inhibit prostate cancer stem cell characteristics, invasion, migration and epithelial-mesenchymal transition.

Q2 Biochemistry, Genetics and Molecular Biology
Su-Ni Tang, Chandan Singh, Dara Nall, Daniel Meeker, Sharmila Shankar, Rakesh K Srivastava
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引用次数: 189

Abstract

Background: Much attention has been recently focused on the role of cancer stem cells (CSCs) in the initiation and progression of solid malignancies. Since CSCs are able to proliferate and self-renew extensively due to their ability to express anti-apoptotic and drug resistant proteins, thus sustaining tumor growth. Therefore, the strategy to eradicate CSCs might have significant clinical implications. The objectives of this study were to examine the molecular mechanisms by which epigallocathechin gallate (EGCG) inhibits stem cell characteristics of prostate CSCs, and synergizes with quercetin, a major polyphenol and flavonoid commonly detected in many fruits and vegetables.

Results: Our data indicate that human prostate cancer cell lines contain a small population of CD44+CD133+ cancer stem cells and their self-renewal capacity is inhibited by EGCG. Furthermore, EGCG inhibits the self-renewal capacity of CD44+alpha2beta1+CD133+ CSCs isolated from human primary prostate tumors, as measured by spheroid formation in suspension. EGCG induces apoptosis by activating capase-3/7 and inhibiting the expression of Bcl-2, survivin and XIAP in CSCs. Furthermore, EGCG inhibits epithelial-mesenchymal transition by inhibiting the expression of vimentin, slug, snail and nuclear beta-catenin, and the activity of LEF-1/TCF responsive reporter, and also retards CSC's migration and invasion, suggesting the blockade of signaling involved in early metastasis. Interestingly, quercetin synergizes with EGCG in inhibiting the self-renewal properties of prostate CSCs, inducing apoptosis, and blocking CSC's migration and invasion. These data suggest that EGCG either alone or in combination with quercetin can eliminate cancer stem cell-characteristics.

Conclusion: Since carcinogenesis is a complex process, combination of bioactive dietary agents with complementary activities will be beneficial for prostate cancer prevention and/ortreatment.

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生物类黄酮槲皮素与没食子儿茶素没食子酸酯(EGCG)协同抑制前列腺癌干细胞特性、侵袭、迁移和上皮-间质转化。
背景:近年来,肿瘤干细胞(CSCs)在实体恶性肿瘤的发生和发展中的作用受到了广泛关注。由于CSCs能够表达抗凋亡和耐药蛋白,因此能够广泛增殖和自我更新,从而维持肿瘤的生长。因此,根除csc的策略可能具有重要的临床意义。本研究的目的是研究表没食子儿茶素没食子酸酯(EGCG)抑制前列腺干细胞特征的分子机制,并与槲皮素协同作用,槲皮素是一种主要的多酚和类黄酮,常见于许多水果和蔬菜中。结果:我们的数据表明,人类前列腺癌细胞系含有少量CD44+CD133+癌症干细胞,它们的自我更新能力受到EGCG的抑制。此外,EGCG抑制从人原发性前列腺肿瘤中分离的CD44+alpha2beta1+CD133+ CSCs的自我更新能力,通过悬浮球体形成来测量。EGCG通过激活capase-3/7,抑制CSCs中Bcl-2、survivin和XIAP的表达诱导细胞凋亡。此外,EGCG通过抑制vimentin、slug、snail和细胞核β -catenin的表达以及LEF-1/TCF应答报告蛋白的活性,抑制上皮-间质转化,并延缓CSC的迁移和侵袭,提示阻断了参与早期转移的信号通路。有趣的是,槲皮素与EGCG协同抑制前列腺CSC的自我更新特性,诱导细胞凋亡,阻断CSC的迁移和侵袭。这些数据表明,EGCG单独使用或与槲皮素联合使用都可以消除癌症干细胞特征。结论:由于前列腺癌的发生是一个复杂的过程,生物活性膳食制剂与补充活性膳食制剂的结合将有利于前列腺癌的预防和/或治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Signaling
Journal of Molecular Signaling Biochemistry, Genetics and Molecular Biology-Biochemistry
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期刊介绍: Journal of Molecular Signaling is an open access, peer-reviewed online journal that encompasses all aspects of molecular signaling. Molecular signaling is an exponentially growing field that encompasses different molecular aspects of cell signaling underlying normal and pathological conditions. Specifically, the research area of the journal is on the normal or aberrant molecular mechanisms involving receptors, G-proteins, kinases, phosphatases, and transcription factors in regulating cell proliferation, differentiation, apoptosis, and oncogenesis in mammalian cells. This area also covers the genetic and epigenetic changes that modulate the signaling properties of cells and the resultant physiological conditions.
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