Tong Kehui, Xin Chang, Chen Wenzhong
Department of Oncological Surgery, Yinzhou People's Hospital, School of Medicine, Ningbo University, Ningbo, Zhejiang 315040, P.R. China.
Department of Hepatobiliary Surgery, Yinzhou People's Hospital, School of Medicine, Ningbo University, Ningbo, Zhejiang 315040, P.R. China.
Oncol Lett. 2017 Jan;13(1):518-524. doi: 10.3892/ol.2016.5387. Epub 2016 Nov 15.
The present study was designed to investigate the antiproliferative activity of isoimperatorin against SGC-7901 cells and to examine the possible mechanisms. The antiproliferative activity of isoimperatorin against SGC-7901 cells was evaluated using an MTT assay, and the mechanisms were investigated using flow cytometry and western blot assays, which were used to determine the apoptotic rate and expression levels of mitochondria-mediated apoptosis-associated proteins, including Survivin, myeloid leukemia cell-1 (Mcl-1), B cell lymphoma-extra large (Bcl-xl), B cell lymphoma 2 (Bcl-2), second mitochondria-derived activator of caspase (Smac), Bcl-2-associated X factor (Bax), cleaved (c)-caspase-3 and c-caspase-9 in SGC-7901 cells. Additionally, a xenograft assay was used to confirm whether isoimperatorin had an inhibitory effect on SGC-7901 cell-induced tumors . The results of the MTT assay suggested that isoimperatorin significantly inhibited the proliferation of SGC-7901 cells in a dose- and time-dependent manner, and the half maximal inhibitory concentration was 18.75 µg/ml. The results of the flow cytometric analysis indicated that, following treatment with isoimperatorin, the apoptotic rate of SGC-7901 cells was significantly increased, compared with that of cells in the control group. The results of the western blot analysis indicated that, following treatment with isoimperatorin, the expression levels of the pro-apoptotic proteins, Bax, c-caspase-3 and c-caspase-9, were significantly increased and the expression levels of the anti-apoptotic proteins, Survivin and Bcl-2, were significantly reduced, compared with the control group. No alterations in expression were found in the other apoptosis-associated proteins, including Mcl-1, Bcl-xl and Smac. The results of the xenograft assay indicated that isoimperatorin significantly inhibited the growth of SGC-7901 cell-induced tumor by increasing the expression levels of pro-apoptotic proteins (Bax, c-caspase-3 and c-caspase-9) and reducing the expression levels of anti-apoptotic proteins (Survivin and Bcl-2) without adverse effects on the increasing body weight of nude mice. In conclusion, the present study revealed that isoimperatorin may be able to induce the apoptosis of SGC-7901 cells and by regulating the expression levels of mitochondria-mediated apoptosis-associated proteins.
本研究旨在探讨异欧前胡素对SGC - 7901细胞的抗增殖活性,并研究其可能的作用机制。采用MTT法评估异欧前胡素对SGC - 7901细胞的抗增殖活性,运用流式细胞术和蛋白质免疫印迹法研究其作用机制,以确定SGC - 7901细胞中线粒体介导的凋亡相关蛋白的凋亡率和表达水平,这些蛋白包括生存素、髓样白血病细胞-1(Mcl - 1)、B细胞淋巴瘤-特大(Bcl - xl)、B细胞淋巴瘤2(Bcl - 2)、第二线粒体衍生的半胱天冬酶激活剂(Smac)、Bcl - 2相关X因子(Bax)、裂解的(c)-半胱天冬酶-3和c-半胱天冬酶-9。此外,采用异种移植试验来确认异欧前胡素是否对SGC - 7901细胞诱导的肿瘤具有抑制作用。MTT试验结果表明,异欧前胡素以剂量和时间依赖性方式显著抑制SGC - 7901细胞的增殖,半数最大抑制浓度为18.75μg/ml。流式细胞术分析结果表明,用异欧前胡素处理后,SGC - 7901细胞的凋亡率与对照组细胞相比显著增加。蛋白质免疫印迹分析结果表明,用异欧前胡素处理后,与对照组相比,促凋亡蛋白Bax、c-半胱天冬酶-3和c-半胱天冬酶-9的表达水平显著增加,抗凋亡蛋白生存素和Bcl - 2的表达水平显著降低。在其他凋亡相关蛋白,包括Mcl - 1、Bcl - xl和Smac中未发现表达改变。异种移植试验结果表明,异欧前胡素通过增加促凋亡蛋白(Bax、c-半胱天冬酶-3和c-半胱天冬酶-9)的表达水平和降低抗凋亡蛋白(生存素和Bcl - 2)的表达水平,显著抑制SGC - 7901细胞诱导的肿瘤生长,且对裸鼠体重增加无不良影响。总之,本研究表明异欧前胡素可能能够通过调节线粒体介导的凋亡相关蛋白的表达水平诱导SGC - 7901细胞凋亡。