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发酵大豆饮料(Q-CAN® PLUS)诱导癌细胞凋亡并降低其活力。

Fermented Soy Drink (Q-CAN® PLUS) Induces Apoptosis and Reduces Viability of Cancer Cells.

机构信息

Department of Internal Medicine (Digestive Diseases), Yale University School of Medicine, New Haven, CT, USA.

Hartford Hospital and University of Connecticut, Hartford, CT, USA.

出版信息

Nutr Cancer. 2022;74(10):3670-3678. doi: 10.1080/01635581.2022.2077385. Epub 2022 May 23.

Abstract

This study tested the ability of a fermented soy product to induce tumor cell toxicity and to assess if this was due to fermentation of soy, and to the genistein content. Four cancer cell lines were cultured without additive, with fermented soy (Q-CAN® PLUS), nonfermented soy, or genistein, and cell viability was examined at 24 h, 48 h, and 72 h. The sensitivity of the cell lines to apoptosis by Q-CAN PLUS was tested with the Annexin V assay. All cell lines demonstrated a dose and time response reduction in tumor cell viability with exposure to Q-CAN PLUS (IC at 24 h 3.8 mg/mL to 9 mg/mL). Unfermented soy did not show reduction in viability of any cell line within the same concentration range. The IC of genistein for each of the cell lines was significantly greater than for Q-CAN PLUS. All four tumor cell lines demonstrated apoptosis in response to Q-CAN PLUS. Q-CAN PLUS reduces viability and increases apoptosis of cancer cells in a concentration- and fermentation-dependent manner. Taking into consideration the IC of genistein and the concentration of genistein in Q-CAN PLUS, the genistein content of Q-CAN PLUS is not responsible for the majority reduction in tumor cell viability. This suggests that fermentation of soy results in the production of metabolites that reduce cancer cell viability and induce cellular apoptosis, and play a major role in addition to any effects produced by their genistein content.

摘要

这项研究测试了一种发酵大豆产品诱导肿瘤细胞毒性的能力,并评估其是否归因于大豆的发酵以及染料木黄酮的含量。将四种癌细胞系在无添加剂、发酵大豆(Q-CAN® PLUS)、非发酵大豆或染料木黄酮的情况下培养,并在 24 小时、48 小时和 72 小时时检查细胞活力。通过 Annexin V 测定法测试 Q-CAN PLUS 对细胞凋亡的敏感性。所有细胞系均显示出与 Q-CAN PLUS 接触时肿瘤细胞活力的剂量和时间反应减少(24 小时的 IC 为 3.8 mg/mL 至 9 mg/mL)。在相同浓度范围内,未发酵的大豆未显示出任何细胞系活力的降低。每种细胞系的染料木黄酮的 IC 均明显大于 Q-CAN PLUS。所有四种肿瘤细胞系均对 Q-CAN PLUS 表现出凋亡。Q-CAN PLUS 以浓度和发酵依赖性方式降低癌细胞活力并增加细胞凋亡。考虑到染料木黄酮的 IC 和 Q-CAN PLUS 中染料木黄酮的浓度,Q-CAN PLUS 中的染料木黄酮含量并不是导致肿瘤细胞活力大部分降低的原因。这表明大豆的发酵导致产生了代谢产物,这些代谢产物降低了癌细胞活力并诱导细胞凋亡,并且除了其染料木黄酮含量产生的任何作用之外,还发挥了主要作用。

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