Ginkgo biloba extract induce cell apoptosis and G0/G1 cycle arrest in gastric cancer cells.

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-11-15 eCollection Date: 2015-01-01
Yu Bai, Feng Zhao, Yan Li, Lei Wang, Xiang-Jie Fang, Chen-Yu Wang
{"title":"Ginkgo biloba extract induce cell apoptosis and G0/G1 cycle arrest in gastric cancer cells.","authors":"Yu Bai, Feng Zhao, Yan Li, Lei Wang, Xiang-Jie Fang, Chen-Yu Wang","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Previous studies have shown that the Ginkgo biloba extract (EGb761) can be used to anti-cancer. However, the mechanism by which EGb761 mediate this effect is still unclear. In the present study, EGb761 inhibited cell proliferation and induced cell apoptosis in gastric cancer cell was explored.</p><p><strong>Methods: </strong>The cell viability was detected by the CCK8 assay. The cell cycle and apoptosis was assessed by flow cytometry. The protein expression of caspase-3, p53 and Bcl-2 were analyzed by western blot.</p><p><strong>Results: </strong>Treatment of human gastric cancer cells with EGb761 induced cell death in a dose-dependent manner by using CCK8 assay. Consistent with the CCK8 assay, the flow cytometry results showed that gastric cancer cells were accumulated in G0/G1 phase when exposed to EGb761. Furthermore, the proportion of apoptosis cells was increased after EGb761 treatment as compared to untreated group. In addition, our results showed that the treatment of AGS cells with EGb761 significantly increased the expression of caspase3 and p53, and decreased the anti-apoptotic Bcl-2 level.</p><p><strong>Conclusions: </strong>Our results demonstrated that EGb761 could inhibit gastric cancer proliferation through adjusting cell cycle and inducing cell apoptosis.</p>","PeriodicalId":13892,"journal":{"name":"International journal of clinical and experimental medicine","volume":"8 11","pages":"20977-82"},"PeriodicalIF":0.2000,"publicationDate":"2015-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723873/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of clinical and experimental medicine","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Previous studies have shown that the Ginkgo biloba extract (EGb761) can be used to anti-cancer. However, the mechanism by which EGb761 mediate this effect is still unclear. In the present study, EGb761 inhibited cell proliferation and induced cell apoptosis in gastric cancer cell was explored.

Methods: The cell viability was detected by the CCK8 assay. The cell cycle and apoptosis was assessed by flow cytometry. The protein expression of caspase-3, p53 and Bcl-2 were analyzed by western blot.

Results: Treatment of human gastric cancer cells with EGb761 induced cell death in a dose-dependent manner by using CCK8 assay. Consistent with the CCK8 assay, the flow cytometry results showed that gastric cancer cells were accumulated in G0/G1 phase when exposed to EGb761. Furthermore, the proportion of apoptosis cells was increased after EGb761 treatment as compared to untreated group. In addition, our results showed that the treatment of AGS cells with EGb761 significantly increased the expression of caspase3 and p53, and decreased the anti-apoptotic Bcl-2 level.

Conclusions: Our results demonstrated that EGb761 could inhibit gastric cancer proliferation through adjusting cell cycle and inducing cell apoptosis.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
银杏叶提取物可诱导胃癌细胞凋亡和 G0/G1 周期停滞。
研究目的以往的研究表明,银杏叶提取物(EGb761)可用于抗癌。然而,EGb761 的作用机制尚不清楚。本研究探讨了 EGb761 在胃癌细胞中抑制细胞增殖和诱导细胞凋亡的作用:方法:采用 CCK8 检测法检测细胞活力。流式细胞术评估细胞周期和细胞凋亡。结果:CCK8 可诱导胃癌细胞凋亡:结果:采用 CCK8 检测法,EGb761 以剂量依赖性方式诱导人胃癌细胞死亡。与 CCK8 试验结果一致,流式细胞术结果显示,暴露于 EGb761 的胃癌细胞在 G0/G1 期积累。此外,与未处理组相比,EGb761 处理后凋亡细胞的比例增加。此外,我们的研究结果表明,用EGb761处理AGS细胞可显著增加caspase3和p53的表达,并降低抗凋亡的Bcl-2水平:我们的研究结果表明,EGb761可通过调整细胞周期和诱导细胞凋亡来抑制胃癌细胞的增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊介绍: Information not localized
期刊最新文献
A case report of moderate COVID-19 with an extremely long-term viral shedding period in China Lentivirus-Mediated knockdown of tectonic family member 1 inhibits medulloblastoma cell proliferation [Retraction]. Classification of MRI and psychological testing data based on support vector machine. Nucleostemin regulates proliferation and migration of gastric cancer and correlates with its malignancy [Retraction]. Effect of lipiodol and methylene blue on the thoracoscopic preoperative positioning [Retraction].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1