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芍药苷抑制人肝癌细胞的肿瘤侵袭和转移。

Paeoniflorin inhibited the tumor invasion and metastasis in human hepatocellular carcinoma cells.

作者信息

Lu J T, He W, Song S S, Wei W

出版信息

Bratisl Lek Listy. 2014;115(7):427-33. doi: 10.4149/bll_2014_084.

Abstract

OBJECTIVE

Evidence suggests that paeoniflorin may be involved in anticancer activities. Here, we have investigated the effects of paeoniflorin and correlative mechanisms on anti-invasion and anti-metastasis in human hepatocellular carcinoma (HCC) cell lines.

MATERIALS AND METHODS

In the current study, we have applied 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) assay to determine the proliferative effect of HepG2 and Bel-7402, two human hepatoma cell lines, and we have established a boyden chamber assay, a wound healing assay and cell adhesion assay to detect and quantify the invasion, metastasis and adhesion of both HepG2 and Bel-7402. In addition, we have analyzed the protein expression of matrix metalloproteinas (MMP)-9, E-cadherin (E-cad) and extracellular signal-regulated kinase (ERK) in both cell lines through western blot analysis.

RESULTS

Paeoniflorin (6. 25-200 µM) had inhibitory effect on the growth of HepG2 and Bel-7402 cell lines, and reduced significantly invasion, metastasis and adhesion of HCC cell lines. In addition, paeoniflorin decreased the expression of MMP-9 and ERK in HepG2 and Bel-7402 cells, and increased expression of E-cad in both cell lines.

CONCLUSIONS

Paeoniflorin is effective anti-metastatic and anti-invasive agent for suppressing HCC invasion and metastasis (Fig. 5, Ref. 30).

摘要

目的

有证据表明芍药苷可能参与抗癌活动。在此,我们研究了芍药苷对人肝癌(HCC)细胞系抗侵袭和抗转移的影响及其相关机制。

材料与方法

在本研究中,我们应用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法测定两种人肝癌细胞系HepG2和Bel-7402的增殖作用,并建立了博伊登小室试验、伤口愈合试验和细胞黏附试验来检测和量化HepG2和Bel-7402的侵袭、转移和黏附情况。此外,我们通过蛋白质印迹分析来检测两种细胞系中基质金属蛋白酶(MMP)-9、E-钙黏蛋白(E-cad)和细胞外信号调节激酶(ERK)的蛋白表达。

结果

芍药苷(6.25 - 200μM)对HepG2和Bel-7402细胞系的生长有抑制作用,并显著降低了肝癌细胞系的侵袭、转移和黏附能力。此外,芍药苷降低了HepG2和Bel-7402细胞中MMP-9和ERK的表达,并增加了两种细胞系中E-cad的表达。

结论

芍药苷是一种有效的抗转移和抗侵袭药物,可抑制肝癌的侵袭和转移(图5,参考文献30)。

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