• 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

伊立替康(CPT-11)耐药激活表皮生长因子受体/核因子 κB,增加 LoVo 结肠癌细胞的细胞转移和自噬。

Resistance to irinotecan (CPT-11) activates epidermal growth factor receptor/nuclear factor kappa B and increases cellular metastasis and autophagy in LoVo colon cancer cells.

机构信息

Graduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan, ROC; Puli Branch, Taichung Veterans General Hospital, Nantou, Taiwan, ROC.

Graduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan, ROC.

出版信息

Cancer Lett. 2014 Jul 10;349(1):51-60. doi: 10.1016/j.canlet.2014.03.023. Epub 2014 Apr 12.

DOI:10.1016/j.canlet.2014.03.023
PMID:24726344
Abstract

Chemotherapy is usually applied to treat colon cancer but leads to chemoresistance, and increased metastasis and invasion. The main focus of this study is to observe effects of resistance to irinotecan (CPT-11) on metastasis, invasion and autophagy in CPT-11 resistant (CPT-11-R) LoVo colon cancer cells. CPT-11, a topoisomerase I inhibitor and a first-line chemotherapeutic drug, is used to treat colon cancer. CPT-11-R cells were constructed in a step-wise fashion with increasing CPT-11 doses. The CPT-11-R strain had a significantly lower expression of Wnt/β-catenin pathway, but induced an EGFR/IKKα/β/NF-κB pathway with elevated cell cycle, metastasis and basal autophagy.

摘要

化疗通常用于治疗结肠癌,但会导致化疗耐药性,并增加转移和侵袭。本研究的主要重点是观察伊立替康(CPT-11)耐药性对 CPT-11 耐药(CPT-11-R)LoVo 结肠癌细胞转移、侵袭和自噬的影响。CPT-11 是拓扑异构酶 I 抑制剂和一线化疗药物,用于治疗结肠癌。通过逐步增加 CPT-11 剂量构建 CPT-11-R 细胞。CPT-11-R 株中 Wnt/β-catenin 通路表达明显降低,但诱导 EGFR/IKKα/β/NF-κB 通路,细胞周期、转移和基础自噬增加。

相似文献

1
Resistance to irinotecan (CPT-11) activates epidermal growth factor receptor/nuclear factor kappa B and increases cellular metastasis and autophagy in LoVo colon cancer cells.伊立替康(CPT-11)耐药激活表皮生长因子受体/核因子 κB,增加 LoVo 结肠癌细胞的细胞转移和自噬。
Cancer Lett. 2014 Jul 10;349(1):51-60. doi: 10.1016/j.canlet.2014.03.023. Epub 2014 Apr 12.
2
Inhibition of NF-κB and metastasis in irinotecan (CPT-11)-resistant LoVo colon cancer cells by thymoquinone via JNK and p38.通过 JNK 和 p38 途径,百里醌抑制伊立替康(CPT-11)耐药 LoVo 结肠癌细胞中的 NF-κB 和转移。
Environ Toxicol. 2017 Feb;32(2):669-678. doi: 10.1002/tox.22268. Epub 2016 Apr 5.
3
The dual EGFR/HER-2 tyrosine kinase inhibitor lapatinib sensitizes colon and gastric cancer cells to the irinotecan active metabolite SN-38.双靶点表皮生长因子受体/人表皮生长因子受体2酪氨酸激酶抑制剂拉帕替尼可使结肠癌细胞和胃癌细胞对伊立替康的活性代谢产物SN-38敏感。
Int J Cancer. 2009 Dec 15;125(12):2957-69. doi: 10.1002/ijc.24658.
4
Bromoethylindole (BEI-9) redirects NF-κB signaling induced by camptothecin and TNFα to promote cell death in colon cancer cells.溴乙靛(BEI-9)将喜树碱和 TNFα 诱导的 NF-κB 信号重定向到促进结肠癌细胞死亡。
Apoptosis. 2017 Dec;22(12):1553-1563. doi: 10.1007/s10495-017-1427-6.
5
Synergistic interaction between the EGFR tyrosine kinase inhibitor gefitinib ("Iressa") and the DNA topoisomerase I inhibitor CPT-11 (irinotecan) in human colorectal cancer cells.表皮生长因子受体(EGFR)酪氨酸激酶抑制剂吉非替尼(“易瑞沙”)与DNA拓扑异构酶I抑制剂CPT-11(伊立替康)在人结肠癌细胞中的协同相互作用。
Int J Cancer. 2004 Jan 20;108(3):464-72. doi: 10.1002/ijc.11539.
6
Inducible chemoresistance to 7-ethyl-10-[4-(1-piperidino)-1-piperidino]-carbonyloxycamptothe cin (CPT-11) in colorectal cancer cells and a xenograft model is overcome by inhibition of nuclear factor-kappaB activation.通过抑制核因子-κB激活可克服大肠癌细胞及异种移植模型中对7-乙基-10-[4-(1-哌啶基)-1-哌啶基]-羰氧基喜树碱(CPT-11)的诱导性化学抗性。
Cancer Res. 2000 May 1;60(9):2323-30.
7
[Experimental study of effect of epidermal growth factor receptor tyrosine kinase inhibitor ZD1839 in combination with irinotecan].表皮生长因子受体酪氨酸激酶抑制剂ZD1839联合伊立替康作用的实验研究
Zhonghua Zhong Liu Za Zhi. 2006 Aug;28(8):578-82.
8
Dual inhibition of epidermal growth factor receptor and vascular endothelial growth factor receptor phosphorylation by AEE788 reduces growth and metastasis of human colon carcinoma in an orthotopic nude mouse model.AEE788对表皮生长因子受体和血管内皮生长因子受体磷酸化的双重抑制作用可降低原位裸鼠模型中人类结肠癌的生长和转移。
Cancer Res. 2005 May 1;65(9):3716-25. doi: 10.1158/0008-5472.CAN-04-3700.
9
Pharmacological targeting of NF-kappaB potentiates the effect of the topoisomerase inhibitor CPT-11 on colon cancer cells.对核因子-κB进行药物靶向作用可增强拓扑异构酶抑制剂CPT-11对结肠癌细胞的作用。
Br J Cancer. 2008 Jan 29;98(2):335-44. doi: 10.1038/sj.bjc.6604082. Epub 2008 Jan 8.
10
SENP1 participates in Irinotecan resistance in human colon cancer cells.SENP1 参与人结肠癌细胞对伊立替康的耐药性。
J Cell Biochem. 2021 Oct;122(10):1277-1294. doi: 10.1002/jcb.29946. Epub 2021 May 26.

引用本文的文献

1
Aniline TFPA enhances camptothecin-induced anti-NSCLC by modulating oxidative stress and impairing autophagy.苯胺TFPA通过调节氧化应激和损害自噬来增强喜树碱诱导的抗非小细胞肺癌作用。
Cancer Cell Int. 2025 Mar 7;25(1):81. doi: 10.1186/s12935-025-03657-6.
2
Overcoming Irinotecan Resistance by Targeting Its Downstream Signaling Pathways in Colon Cancer.通过靶向结肠癌中伊立替康的下游信号通路克服伊立替康耐药性
Cancers (Basel). 2024 Oct 15;16(20):3491. doi: 10.3390/cancers16203491.
3
The topoisomerase inhibitor CPT-11 prevents the growth and metastasis of lung cancer cells in nude mice by inhibiting EGFR/MAPK signaling pathway.
拓扑异构酶抑制剂CPT-11通过抑制EGFR/MAPK信号通路来阻止裸鼠体内肺癌细胞的生长和转移。
Heliyon. 2023 Apr 27;9(5):e15805. doi: 10.1016/j.heliyon.2023.e15805. eCollection 2023 May.
4
Resistance to TOP-1 Inhibitors: Good Old Drugs Still Can Surprise Us.对拓扑异构酶 I 抑制剂的耐药性:老药仍能给我们带来惊喜。
Int J Mol Sci. 2023 Apr 13;24(8):7233. doi: 10.3390/ijms24087233.
5
Topoisomerase I poisons-induced autophagy: Cytoprotective, Cytotoxic or Non-protective.拓扑异构酶I抑制剂诱导的自噬:细胞保护、细胞毒性还是无保护作用
Autophagy Rep. 2023;2(1):1-16. doi: 10.1080/27694127.2022.2155904. Epub 2022 Dec 25.
6
Synthesis of novel 10,11-methylenedioxy-camptothecin glycoside derivatives and investigation of their anti-tumor effects .新型10,11-亚甲二氧基-喜树碱糖苷衍生物的合成及其抗肿瘤作用研究
RSC Adv. 2019 Apr 9;9(20):11142-11150. doi: 10.1039/c9ra00315k.
7
Chemoresistance-Associated Silencing of miR-4454 Promotes Colorectal Cancer Aggression through the and Pathway.miR-4454的化学抗性相关沉默通过[具体通路]促进结直肠癌侵袭。 (注:原文中“and Pathway”部分信息缺失)
Cancers (Basel). 2020 May 14;12(5):1231. doi: 10.3390/cancers12051231.
8
Irinotecan Induces Autophagy-Dependent Apoptosis and Positively Regulates ROS-Related JNK- and P38-MAPK Pathways in Gastric Cancer Cells.伊立替康诱导胃癌细胞发生自噬依赖性凋亡,并正向调控与活性氧相关的JNK和P38丝裂原活化蛋白激酶信号通路。
Onco Targets Ther. 2020 Apr 2;13:2807-2817. doi: 10.2147/OTT.S240803. eCollection 2020.
9
In Vitro and In Silico Mechanistic Insights into miR-21-5p-Mediated Topoisomerase Drug Resistance in Human Colorectal Cancer Cells.miR-21-5p 介导的人结直肠癌细胞拓扑异构酶药物耐药的体外和计算机模拟机制研究
Biomolecules. 2019 Sep 9;9(9):467. doi: 10.3390/biom9090467.
10
FL118, a novel camptothecin analogue, overcomes irinotecan and topotecan resistance in human tumor xenograft models.新型喜树碱类似物FL118在人肿瘤异种移植模型中克服了伊立替康和拓扑替康耐药性。
Am J Transl Res. 2015 Oct 15;7(10):1765-81. eCollection 2015.