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红高粱衍生的脱氧花青素及其O-β-D-葡萄糖苷对PC-3前列腺癌细胞中E-钙黏蛋白启动子活性的影响

Effects of Red Sorghum-Derived Deoxyanthocyanidins and Their O-β-D-Glucosides on E-Cadherin Promoter Activity in PC-3 Prostate Cancer Cells.

作者信息

Mora Nathalie, Rosa Maxence, Touaibia Mohamed, Martin Luc J

机构信息

UMR408 INRA-UAPV, SQPO, Qualim, University Avignon, Campus Jean-Henri Fabre, Pôle Agrosciences, 301, Rue Baruch de Spinoza, 84911 Avignon, France.

Chemistry and Biochemistry Department, Université de Moncton, Moncton, NB E1A 3E9, Canada.

出版信息

Molecules. 2024 Apr 21;29(8):1891. doi: 10.3390/molecules29081891.

Abstract

Although much less common than anthocyanins, 3-Deoxyanthocyanidins (3-DAs) and their glucosides can be found in cereals such as red sorghum. It is speculated that their bioavailability is higher than that of anthocyanins. Thus far, little is known regarding the therapeutic effects of 3-DAs and their O-β-D-glucosides on cancer, including prostate cancer. Thus, we evaluated their potential to decrease cell viability, to modulate the activity of transcription factors such as NFκB, CREB, and SOX, and to regulate the expression of the gene , encoding E-Cadherin. We found that 4',7-dihydroxyflavylium chloride (P7) and the natural apigeninidin can reduce cell viability, whereas 4',7-dihydroxyflavylium chloride (P7) and 4'-hydroxy-7-O-β-D-glucopyranosyloxyflavylium chloride (P3) increase the activities of NFkB, CREB, and SOX transcription factors, leading to the upregulation of promoter activity in PC-3 prostate cancer cells. Thus, these compounds may contribute to the inhibition of the epithelial-to-mesenchymal transition in cancer cells and prevent the metastatic activity of more aggressive forms of androgen-resistant prostate cancer.

摘要

虽然3-脱氧花青素(3-DAs)及其糖苷比花青素少见得多,但在诸如红高粱等谷物中可以找到它们。据推测,它们的生物利用度高于花青素。到目前为止,关于3-DAs及其O-β-D-葡萄糖苷对癌症(包括前列腺癌)的治疗作用知之甚少。因此,我们评估了它们降低细胞活力、调节转录因子如NFκB、CREB和SOX的活性以及调节编码E-钙黏蛋白的基因表达的潜力。我们发现,4',7-二羟基氯化黄酮(P7)和天然芹菜苷配基可以降低细胞活力,而4',7-二羟基氯化黄酮(P7)和4'-羟基-7-O-β-D-吡喃葡萄糖氧基氯化黄酮(P3)会增加NFkB、CREB和SOX转录因子的活性,导致PC-3前列腺癌细胞中启动子活性上调。因此,这些化合物可能有助于抑制癌细胞的上皮-间质转化,并防止更具侵袭性的雄激素抵抗性前列腺癌形式的转移活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c901/11054106/fc27688b198c/molecules-29-01891-sch001.jpg

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