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石榴提取物抑制体外 MMTV-Wnt-1 小鼠乳腺肿瘤干细胞的增殖和活力。

Pomegranate extract inhibits the proliferation and viability of MMTV-Wnt-1 mouse mammary cancer stem cells in vitro.

机构信息

Department of Nutritional Sciences, School of Human Ecology, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Oncol Rep. 2010 Oct;24(4):1087-91.

Abstract

Pomegranate (Punica granatum L.) is known to possess anticancer activities. The effects of a standardized extract of pomegranate (PE) on a mouse mammary cancer cell line (designated WA4) derived from mouse MMTV-Wnt-1 mammary tumors were examined in this study. The WA4 cell line has been previously characterized as containing a majority of cells possessing stem cell characteristics. PE inhibited the proliferation of WA4 cells in a time- and concentration-dependent manner. This was due to an arrest of cell cycle progression in the G0/G1 phase. PE was also cytotoxic to quiescent WA4 cells in a concentration-dependent manner at concentrations >10 microg/ml. PE treatment of WA4 cells resulted in an increase in caspase-3 enzyme activity in a time- and concentration-dependent manner, indicating that the cytotoxic effect of PE was due to the induction of apoptosis. We tested the effect of several individual phytochemicals derived from PE on WA4 cells. Ellagic acid, ursolic acid and luteolin caused a time- and concentration-dependent reduction of cell proliferation and viability, suggesting that they contribute to the inhibitory effect of PE, while caffeic acid had no effect. Cancer stem cells, which are highly resistant to conventional chemotherapeutic agents, are thought to be the origin of both primary and secondary breast tumors, and thus are a critical target in both breast cancer therapy and prevention. These data suggest that PE, which is a proven and safe dietary supplement, has promise as an treatment against breast cancer by preventing proliferation of cancer stem cells.

摘要

石榴(Punica granatum L.)被认为具有抗癌活性。本研究旨在研究石榴(PE)标准化提取物对源自鼠 MMTV-Wnt-1 乳腺肿瘤的鼠乳腺癌细胞系(命名为 WA4)的影响。WA4 细胞系先前被表征为包含大多数具有干细胞特征的细胞。PE 以时间和浓度依赖的方式抑制 WA4 细胞的增殖。这是由于细胞周期停滞在 G0/G1 期。PE 以浓度依赖的方式对静止的 WA4 细胞也具有细胞毒性,浓度>10μg/ml。PE 处理 WA4 细胞导致 caspase-3 酶活性呈时间和浓度依赖性增加,表明 PE 的细胞毒性作用是由于诱导细胞凋亡所致。我们测试了几种源自 PE 的单个植物化学物质对 WA4 细胞的影响。鞣花酸、熊果酸和木犀草素导致细胞增殖和活力呈时间和浓度依赖性降低,表明它们有助于 PE 的抑制作用,而咖啡酸没有作用。癌症干细胞对常规化疗药物具有高度抵抗力,被认为是原发性和继发性乳腺癌的起源,因此是乳腺癌治疗和预防的关键靶点。这些数据表明,PE 作为一种经过验证且安全的膳食补充剂,通过防止癌症干细胞的增殖,有望成为治疗乳腺癌的方法。

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