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前列腺素 E(2)和 F(2)(α)恢复白藜芦醇对培养肝癌细胞侵袭的抑制作用。

Restoration by Prostaglandins E(2) and F (2) (alpha) of Resveratrol-Induced Suppression of Hepatoma Cell Invasion in Culture.

机构信息

Department of Applied Biological Science, Tokyo Noko University, Saiwaicho 3-5-8, Fuchu, Tokyo, 183-8509, Japan.

出版信息

Cytotechnology. 2003 Nov;43(1-3):155-9. doi: 10.1023/b:cyto.0000039903.22449.79.

DOI:10.1023/b:cyto.0000039903.22449.79
PMID:19003221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3449602/
Abstract

In our previous study, resveratrol, a polyphenolic compound in grapes with antioxidative property, and resveratol-loaded rat serum (RS) were found to suppress the invasion of AH109A cells, an ascite hepatoma cell line. The aim of the present study was to investigate whether and which prostaglandins (PGs) would be involved in the invasion of AH109A cells and its suppression by resveratrol and resveratrol-loaded RS, using an in vitro invasion assay system. Not only PGE(2) but also PGF(2) (alpha) stimulated the spontaneous invasion of AH109A cells.They also canceled the resveratrol-induced suppression of hepatoma cell invasion. Results obtained suggest an involvement of PGs, especially PGE(2), in the invasion of hepatoma cells.

摘要

在我们之前的研究中,白藜芦醇,葡萄中的一种具有抗氧化特性的多酚化合物,以及负载白藜芦醇的大鼠血清(RS)被发现能够抑制腹水肝癌细胞系 AH109A 细胞的侵袭。本研究的目的是使用体外侵袭测定系统,探讨白藜芦醇和负载白藜芦醇的 RS 是否以及哪种前列腺素(PG)参与 AH109A 细胞的侵袭及其抑制。不仅 PGE(2),而且 PGF(2)(alpha)刺激 AH109A 细胞的自发侵袭。它们还取消了白藜芦醇诱导的肝癌细胞侵袭抑制。研究结果表明前列腺素,特别是 PGE(2),参与了肝癌细胞的侵袭。

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本文引用的文献

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Cytotechnology. 1997 Jan;23(1-3):127-32. doi: 10.1023/A:1007951231617.
2
Hypolipidemic action of dietary resveratrol, a phytoalexin in grapes and red wine, in hepatoma-bearing rats.膳食白藜芦醇(一种存在于葡萄和红酒中的植物抗毒素)对荷肝癌大鼠的降血脂作用。
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3
Potentiation of invasive activity of hepatoma cells by reactive oxygen species is mediated by autocrine/paracrine loop of hepatocyte growth factor.活性氧对肝癌细胞侵袭活性的增强作用是由肝细胞生长因子的自分泌/旁分泌环路介导的。
Biochem Biophys Res Commun. 2003 May 23;305(1):160-5. doi: 10.1016/s0006-291x(03)00725-3.
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Int J Cancer. 2002 Aug 10;100(5):515-9. doi: 10.1002/ijc.10508.
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