• 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

去甲斑蝥素对人胆囊癌GBC-SD细胞增殖、增殖相关基因蛋白增殖细胞核抗原和Ki-67的影响。

Influence of norcantharidin on proliferation, proliferation-related gene proteins proliferating cell nuclear antigen and Ki-67 of human gallbladder carcinoma GBC-SD cells.

作者信息

Fan Yue-Zu, Fu Jin-Ye, Zhao Ze-Ming, Chen Cun-Qiu

机构信息

Department of Surgery, Tongji Hospital of Tongji University, 389 Xincun Road, Shanghai 200065, China.

出版信息

Hepatobiliary Pancreat Dis Int. 2004 Nov;3(4):603-7.

PMID:15567755
Abstract

BACKGROUND

Gallbladder carcinoma is a highly lethal and aggressive disease with early metastasis, strong invasion and poor prognosis. Most patients with this disease are at the advanced and un-resectable stage and should be considered for palliative treatment such as chemotherapy and radiotherapy. Unfortunately, reports of chemotherapy and radiotherapy for gallbladder carcinoma are disappointing. We investigated the influence of norcantharidin (NCTD) on proliferation, proliferation-related gene proteins PCNA and Ki-67 of human gallbladder carcinoma GBC-SD cells in vitro.

METHODS

GBC-SD cell lines of human gallbladder carcinoma were cultured by the cell culture technique. The experiment was divided into NCTD group and control group. The tetrazolium-based colorimetric assay was used to evaluate cell growth. The streptavidin-biotin complex method was used to determine the expressions of proliferation-related gene proteins PCNA and Ki-67 of human gallbladder carcinoma GBC-SD cells.

RESULTS

NCTD inhibited the growth and proliferation of GBC-SD cells from 10 mg/L or after 6 hours in a dose-and time-dependent manner, with the IC50 value of 56.18 microg/ml at 48 hours. After treatment with NCTD, the expression of PCNA (0.932+/-0.031 vs. 0.318+/-0.023, P<0.001) and Ki-67 (0.964+/-0.092 vs. 0.297+/-0.018, P<0.001) proteins were decreased significantly.

CONCLUSION

NCTD inhibits the proliferation of human gallbladder carcinoma GBC-SD cells in vitro and the expression of their proliferation-related gene proteins PCNA and Ki-67.

摘要

背景

胆囊癌是一种具有早期转移、强侵袭性和不良预后的高致死性侵袭性疾病。大多数该疾病患者处于晚期且不可切除阶段,应考虑进行化疗和放疗等姑息治疗。不幸的是,关于胆囊癌化疗和放疗的报道令人失望。我们在体外研究了去甲斑蝥素(NCTD)对人胆囊癌GBC-SD细胞增殖及增殖相关基因蛋白PCNA和Ki-67的影响。

方法

采用细胞培养技术培养人胆囊癌GBC-SD细胞系。实验分为NCTD组和对照组。采用四氮唑比色法评估细胞生长。采用链霉抗生物素蛋白-生物素复合物法测定人胆囊癌GBC-SD细胞增殖相关基因蛋白PCNA和Ki-67的表达。

结果

NCTD从10mg/L起或6小时后以剂量和时间依赖性方式抑制GBC-SD细胞的生长和增殖,48小时时IC50值为56.18μg/ml。用NCTD处理后,PCNA(0.932±0.031对0.318±0.023,P<0.001)和Ki-67(0.964±0.092对0.297±0.018,P<0.001)蛋白的表达显著降低。

结论

NCTD在体外抑制人胆囊癌GBC-SD细胞的增殖及其增殖相关基因蛋白PCNA和Ki-67的表达。

相似文献

1
Influence of norcantharidin on proliferation, proliferation-related gene proteins proliferating cell nuclear antigen and Ki-67 of human gallbladder carcinoma GBC-SD cells.去甲斑蝥素对人胆囊癌GBC-SD细胞增殖、增殖相关基因蛋白增殖细胞核抗原和Ki-67的影响。
Hepatobiliary Pancreat Dis Int. 2004 Nov;3(4):603-7.
2
Inhibitory effect of norcantharidin on the growth of human gallbladder carcinoma GBC-SD cells in vitro.去甲斑蝥素对人胆囊癌GBC-SD细胞体外生长的抑制作用
Hepatobiliary Pancreat Dis Int. 2007 Feb;6(1):72-80.
3
[The in vitro effect of norcantharidin on proliferation and invasion of human gallbladder carcinoma GBC-SD cells and its mechanism].去甲斑蝥素对人胆囊癌GBC-SD细胞增殖和侵袭的体外作用及其机制
Zhonghua Zhong Liu Za Zhi. 2004 May;26(5):271-4.
4
Effect of norcantharidin on proliferation and invasion of human gallbladder carcinoma GBC-SD cells.去甲斑蝥素对人胆囊癌GBC-SD细胞增殖和侵袭的影响
World J Gastroenterol. 2005 Apr 28;11(16):2431-7. doi: 10.3748/wjg.v11.i16.2431.
5
Norcantharidin inhibits growth of human gallbladder carcinoma xenografted tumors in nude mice by inducing apoptosis and blocking the cell cycle in vivo.去甲斑蝥素通过体内诱导细胞凋亡和阻断细胞周期抑制裸鼠人胆囊癌细胞移植瘤的生长。
Hepatobiliary Pancreat Dis Int. 2010 Aug;9(4):414-22.
6
[Anti-tumor mechanism of norcantharidin for the implanted tumors of human gallbladder carcinoma in nude mice in vivo].去甲斑蝥素对人胆囊癌裸鼠移植瘤的体内抗肿瘤机制
Zhonghua Wai Ke Za Zhi. 2006 May 1;44(9):618-22.
7
[Effects of norcantharidin on angiogenesis of human gallbladder carcinoma and its anti-angiogenic mechanisms].去甲斑蝥素对人胆囊癌血管生成的影响及其抗血管生成机制
Zhonghua Yi Xue Za Zhi. 2006 Mar 14;86(10):693-9.
8
Norcantharidin inhibits tumor growth and vasculogenic mimicry of human gallbladder carcinomas by suppression of the PI3-K/MMPs/Ln-5γ2 signaling pathway.去甲基斑蝥素通过抑制 PI3-K/MMPs/Ln-5γ2 信号通路抑制人胆囊癌细胞的生长和血管生成拟态。
BMC Cancer. 2014 Mar 15;14:193. doi: 10.1186/1471-2407-14-193.
9
Norcantharidin: a potential antiangiogenic agent for gallbladder cancers in vitro and in vivo.去甲斑蝥素:一种潜在的抗胆囊癌血管生成的药物,在体内外均有作用。
Int J Oncol. 2012 May;40(5):1501-14. doi: 10.3892/ijo.2011.1314. Epub 2011 Dec 21.
10
Inhibition of tumor vasculogenic mimicry and prolongation of host survival in highly aggressive gallbladder cancers by norcantharidin via blocking the ephrin type a receptor 2/focal adhesion kinase/paxillin signaling pathway.去甲斑蝥素通过阻断 Ephrin A 型受体 2/粘着斑激酶/桩蛋白信号通路抑制高侵袭性胆囊癌的肿瘤血管生成拟态并延长宿主生存期
PLoS One. 2014 May 8;9(5):e96982. doi: 10.1371/journal.pone.0096982. eCollection 2014.

引用本文的文献

1
Insight into norcantharidin, a small-molecule synthetic compound with potential multi-target anticancer activities.对去甲斑蝥素的深入了解,一种具有潜在多靶点抗癌活性的小分子合成化合物。
Chin Med. 2020 May 29;15:55. doi: 10.1186/s13020-020-00338-6. eCollection 2020.
2
Norcantharidin Suppresses Colon Cancer Cell Epithelial-Mesenchymal Transition by Inhibiting the αvβ6-ERK-Ets1 Signaling Pathway.去甲斑蝥素通过抑制αvβ6-ERK-Ets1信号通路抑制结肠癌细胞上皮-间质转化
Sci Rep. 2016 Feb 5;6:20500. doi: 10.1038/srep20500.
3
DMH1 (4-[6-(4-isopropoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl]quinoline) inhibits chemotherapeutic drug-induced autophagy.
DMH1(4-[6-(4-异丙氧基苯基)吡唑并[1,5-a]嘧啶-3-基]喹啉)可抑制化疗药物诱导的自噬。
Acta Pharm Sin B. 2015 Jul;5(4):330-6. doi: 10.1016/j.apsb.2014.12.010. Epub 2015 Feb 21.
4
Interferon-gamma and interlukin-4 patterns in BALB/c mice suffering from cutaneous leishmaniasis treated with cantharidin.用斑蝥素治疗的患皮肤利什曼病的BALB/c小鼠中γ干扰素和白细胞介素-4模式
Jundishapur J Microbiol. 2014 Jun;7(6):e10907. doi: 10.5812/jjm.10907. Epub 2014 Jun 1.
5
Norcantharidin induced DU145 cell apoptosis through ROS-mediated mitochondrial dysfunction and energy depletion.去甲斑蝥素通过 ROS 介导的线粒体功能障碍和能量耗竭诱导 DU145 细胞凋亡。
PLoS One. 2013 Dec 19;8(12):e84610. doi: 10.1371/journal.pone.0084610. eCollection 2013.
6
Norcantharidin induces HT-29 colon cancer cell apoptosis through the alphavbeta6-extracellular signal-related kinase signaling pathway.去甲斑蝥素通过αvβ6-细胞外信号调节激酶信号通路诱导 HT-29 结肠癌细胞凋亡。
Cancer Sci. 2009 Dec;100(12):2302-8. doi: 10.1111/j.1349-7006.2009.01320.x. Epub 2009 Aug 20.