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纯化的牡荆素化合物 1 抑制人绒癌荷瘤小鼠肿瘤生长并诱导细胞凋亡。

Purified vitexin compound 1 suppresses tumor growth and induces cell apoptosis in a mouse model of human choriocarcinoma.

机构信息

Department of Obstetrics and Gynecology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.

出版信息

Int J Gynecol Cancer. 2012 Mar;22(3):360-6. doi: 10.1097/IGC.0b013e31823de844.

Abstract

OBJECTIVE

In our previous study, we had isolated a series of lignan compounds, termed vitexins, from the seed of Chinese herb Vitex negundo and found broad antitumor activities of these compounds in many cancer xenograft models and cell lines. This study was aimed to determine the antitumor effect of purified vitexin compound 1 (VB1) on choriocarcinoma in vitro and in vivo.

MATERIALS AND METHODS

The severe combined immunodeficiency mouse model of choriocarcinoma was established to investigate the in vivo effect of VB1. Its effect on proliferation and apoptosis in JEG-3 cell line was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, colony formation assay and flow cytometry, respectively. The expression of caspase-3, Bcl-2, and some molecules involved in the mammalian target of rapamycin (mTOR) signaling was detected by Western blot.

RESULTS

Vitexin compound 1 significantly inhibited the growth of choriocarcinoma in severe combined immunodeficient mice and reduced the serum β-human chorionic gonadotropin level. Vitexin compound 1 inhibited cell proliferation, induced apoptosis, and inhibited the mTOR signaling in JEG-3 cell line.

CONCLUSION

Vitexin compound 1 could inhibit choriocarcinoma via inducing cell apoptosis and suppressing the mTOR pathway.

摘要

目的

在我们之前的研究中,我们从中药牡荆的种子中分离出一系列木脂素化合物,称为牡荆素,并发现这些化合物在许多癌症异种移植模型和细胞系中具有广泛的抗肿瘤活性。本研究旨在确定纯化的牡荆素化合物 1(VB1)对绒毛膜癌的体内和体外抗肿瘤作用。

材料与方法

建立严重联合免疫缺陷小鼠绒毛膜癌模型,研究 VB1 的体内作用。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)比色法、集落形成实验和流式细胞术分别评估 VB1 对 JEG-3 细胞系增殖和凋亡的影响。采用 Western blot 检测 caspase-3、Bcl-2 和哺乳动物雷帕霉素靶蛋白(mTOR)信号通路中一些分子的表达。

结果

牡荆素化合物 1 显著抑制严重联合免疫缺陷小鼠绒毛膜癌的生长,并降低血清β-人绒毛膜促性腺激素水平。牡荆素化合物 1 抑制 JEG-3 细胞系的细胞增殖,诱导细胞凋亡,并抑制 mTOR 信号通路。

结论

牡荆素化合物 1 可通过诱导细胞凋亡和抑制 mTOR 通路抑制绒毛膜癌。

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