• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

丹参酮 IIA 在体内外诱导胃癌的生长抑制和凋亡。

Tanshinone IIA induces growth inhibition and apoptosis in gastric cancer in vitro and in vivo.

机构信息

Department of Gastroenterology, Huashan Hospital, Fudan University, Shanghai, PR China.

出版信息

Oncol Rep. 2012 Feb;27(2):523-8. doi: 10.3892/or.2011.1524. Epub 2011 Oct 27.

DOI:10.3892/or.2011.1524
PMID:22038415
Abstract

As a phytochemical derived from the roots of Salvia miltiorrhiza Bunge, Tanshinone IIA has been reported to possess anti-inflammatory and antioxidant activity. Studies in breast, colon, prostate and lung cancer indicate that Tanshinone IIA may exhibit a promising antitumor activity. However, systemic studies of the cytotoxic effects of Tanshinone IIA on gastric cancer have not been described. The present study offers a comprehensive evaluation of the antitumor effects of Tanshinone IIA in gastric cancer cells in vitro and in a mouse xenograft model. Cell viability and apoptosis in vitro were evaluated through the MTT assay and flow cytometry analysis. The results indicate that Tanshinone IIA can induce gastric cancer cell growth inhibition and apoptosis in a time- and concentration-dependent manner. Furthermore, we investigated the mechanism of the apoptotic effects induced by Tanshinone IIA. We found that Tanshinone IIA can not only cause cell cycle arrest in the G2/M phase, but also trigger the intrinsic apoptotic signaling pathway. The results suggest that Tanshinone IIA may serve as an effective adjunctive reagent in the treatment of gastric cancer.

摘要

丹参酮 IIA 是从丹参的根部提取的一种植物化学物质,据报道具有抗炎和抗氧化活性。在乳腺癌、结肠癌、前列腺癌和肺癌中的研究表明,丹参酮 IIA 可能具有有前途的抗肿瘤活性。然而,丹参酮 IIA 对胃癌的细胞毒性作用的系统研究尚未描述。本研究对丹参酮 IIA 在体外和小鼠异种移植模型中对胃癌细胞的抗肿瘤作用进行了全面评估。通过 MTT 检测和流式细胞术分析评估了细胞活力和细胞凋亡。结果表明,丹参酮 IIA 可以时间和浓度依赖的方式诱导胃癌细胞生长抑制和凋亡。此外,我们研究了丹参酮 IIA 诱导细胞凋亡的机制。我们发现,丹参酮 IIA 不仅可以引起细胞周期停滞在 G2/M 期,还可以触发内在凋亡信号通路。结果表明,丹参酮 IIA 可能是治疗胃癌的有效辅助试剂。

相似文献

1
Tanshinone IIA induces growth inhibition and apoptosis in gastric cancer in vitro and in vivo.丹参酮 IIA 在体内外诱导胃癌的生长抑制和凋亡。
Oncol Rep. 2012 Feb;27(2):523-8. doi: 10.3892/or.2011.1524. Epub 2011 Oct 27.
2
Tanshinone I effectively induces apoptosis in estrogen receptor-positive (MCF-7) and estrogen receptor-negative (MDA-MB-231) breast cancer cells.丹参酮I可有效诱导雌激素受体阳性(MCF-7)和雌激素受体阴性(MDA-MB-231)乳腺癌细胞凋亡。
Int J Oncol. 2008 Sep;33(3):485-91.
3
Activation of p53 signaling and inhibition of androgen receptor mediate tanshinone IIA induced G1 arrest in LNCaP prostate cancer cells.丹参酮 IIA 通过激活 p53 信号通路和抑制雄激素受体诱导 LNCaP 前列腺癌细胞 G1 期阻滞。
Phytother Res. 2012 May;26(5):669-74. doi: 10.1002/ptr.3616. Epub 2011 Oct 13.
4
Tanshinone IIA inhibits human prostate cancer cells growth by induction of endoplasmic reticulum stress in vitro and in vivo.丹参酮 IIA 通过诱导内质网应激在体外和体内抑制人前列腺癌细胞生长。
Prostate Cancer Prostatic Dis. 2013 Dec;16(4):315-22. doi: 10.1038/pcan.2013.38. Epub 2013 Sep 17.
5
Potentiation of the anticancer effect of doxorubicinin drug-resistant gastric cancer cells by tanshinone IIA.丹参酮IIA增强阿霉素对耐药胃癌细胞的抗癌作用
Phytomedicine. 2018 Dec 1;51:58-67. doi: 10.1016/j.phymed.2018.05.012. Epub 2018 May 19.
6
Tanshinone IIA inhibits the growth, attenuates the stemness and induces the apoptosis of human glioma stem cells.丹参酮IIA抑制人胶质瘤干细胞的生长,减弱其干性并诱导其凋亡。
Oncol Rep. 2014 Sep;32(3):1303-11. doi: 10.3892/or.2014.3293. Epub 2014 Jun 26.
7
Tanshinone IIA inhibits gastric carcinoma AGS cells through increasing p-p38, p-JNK and p53 but reducing p-ERK, CDC2 and cyclin B1 expression.丹参酮 IIA 通过增加 p-p38、p-JNK 和 p53,同时减少 p-ERK、CDC2 和细胞周期蛋白 B1 的表达来抑制胃癌 AGS 细胞。
Anticancer Res. 2014 Dec;34(12):7097-110.
8
Apoptosis induced by the methanol extract of Salvia miltiorrhiza Bunge in non-small cell lung cancer through PTEN-mediated inhibition of PI3K/Akt pathway.丹参甲醇提取物通过PTEN介导的PI3K/Akt通路抑制作用诱导非小细胞肺癌细胞凋亡。
J Ethnopharmacol. 2017 Mar 22;200:107-116. doi: 10.1016/j.jep.2016.12.051. Epub 2017 Jan 12.
9
A novel compound modified from tanshinone inhibits tumor growth in vivo via activation of the intrinsic apoptotic pathway.一种新型丹参酮化合物通过激活内在凋亡途径抑制体内肿瘤生长。
Cancer Lett. 2010 Nov 1;297(1):18-30. doi: 10.1016/j.canlet.2010.04.020. Epub 2010 May 21.
10
Tanshinone IIA acts via p38 MAPK to induce apoptosis and the down-regulation of ERCC1 and lung-resistance protein in cisplatin-resistant ovarian cancer cells.丹参酮 IIA 通过 p38 MAPK 诱导凋亡及下调顺铂耐药卵巢癌细胞中的 ERCC1 和肺耐药蛋白。
Oncol Rep. 2011 Mar;25(3):781-8. doi: 10.3892/or.2010.1107. Epub 2010 Dec 13.

引用本文的文献

1
Mechanism of Fuzheng Qudu prescription in the treatment of lung cancer based on network pharmacology and experimental validation.基于网络药理学和实验验证的扶正祛毒方治疗肺癌的机制
Heliyon. 2024 Sep 6;10(18):e37546. doi: 10.1016/j.heliyon.2024.e37546. eCollection 2024 Sep 30.
2
transcription factor inhibits tanshinone accumulation in response to ethylene signaling in .转录因子抑制丹参酮在响应乙烯信号时的积累 。 (注:原文句子不完整,推测补充完整后翻译,原句中“in.”应是有遗漏的内容)
Front Plant Sci. 2024 Apr 2;15:1356922. doi: 10.3389/fpls.2024.1356922. eCollection 2024.
3
Tanshinone IIA targeting cell signaling pathways: a plausible paradigm for cancer therapy.
丹参酮 IIA 靶向细胞信号通路:癌症治疗的合理范例。
Pharmacol Rep. 2023 Aug;75(4):907-922. doi: 10.1007/s43440-023-00507-y. Epub 2023 Jul 13.
4
Traditional Chinese medicine for transformation of gastric precancerous lesions to gastric cancer: A critical review.中药对胃癌前病变向胃癌转化的作用:一项批判性综述。
World J Gastrointest Oncol. 2023 Jan 15;15(1):36-54. doi: 10.4251/wjgo.v15.i1.36.
5
in cancer: Potential role in regulating MicroRNAs and epigenetic enzymes.在癌症中:在调节微小RNA和表观遗传酶方面的潜在作用。
Front Pharmacol. 2022 Sep 12;13:1008222. doi: 10.3389/fphar.2022.1008222. eCollection 2022.
6
Dihydrotanshinone I Enhances Cell Adhesion and Inhibits Cell Migration in Osteosarcoma U-2 OS Cells through CD44 and Chemokine Signaling.二氢丹参酮 I 通过 CD44 和趋化因子信号增强骨肉瘤 U-2 OS 细胞的黏附和抑制细胞迁移。
Molecules. 2022 Jun 9;27(12):3714. doi: 10.3390/molecules27123714.
7
Construction and Screening of Fractional Library of Radix et Rhizoma for the Rapid Identification of Active Compounds against Prostate Cancer.用于快速鉴定抗前列腺癌活性化合物的根茎类药材组分库的构建与筛选
J Oncol. 2022 Feb 24;2022:9955834. doi: 10.1155/2022/9955834. eCollection 2022.
8
Anticancer Applications and Pharmacological Properties of Piperidine and Piperine: A Comprehensive Review on Molecular Mechanisms and Therapeutic Perspectives.哌啶和胡椒碱的抗癌应用及药理特性:关于分子机制和治疗前景的综合综述
Front Pharmacol. 2022 Jan 7;12:772418. doi: 10.3389/fphar.2021.772418. eCollection 2021.
9
Cryptotanshinone inhibits proliferation and induces apoptosis of breast cancer MCF-7 cells via GPER mediated PI3K/AKT signaling pathway.隐丹参酮通过 G 蛋白偶联雌激素受体(GPER)介导的 PI3K/AKT 信号通路抑制乳腺癌 MCF-7 细胞的增殖并诱导其凋亡。
PLoS One. 2022 Jan 21;17(1):e0262389. doi: 10.1371/journal.pone.0262389. eCollection 2022.
10
Cryptotanshinone inhibits cytotoxin-associated gene A-associated development of gastric cancer and mucosal erosions.隐丹参酮抑制细胞毒素相关基因A相关的胃癌发展和黏膜糜烂。
World J Gastrointest Oncol. 2021 Jul 15;13(7):693-705. doi: 10.4251/wjgo.v13.i7.693.