• 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

第二代取代喹啉类化合物作为乳腺癌的抗癌药物。

Second-generation substituted quinolines as anticancer drugs for breast cancer.

机构信息

Departments of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS 66506, USA.

出版信息

Anticancer Res. 2010 Oct;30(10):3927-32.

PMID:21036704
Abstract

Cancer cells have reduced capacity for gap junctional inter-cellular communication (GJIC). One feasible approach to reduce growth of cancer cells is to enhance GJIC. This report shows that a second-generation substituted quinoline, PQ7, has anti-tumor effect. Scrape load/dye transfer and colony growth assays were performed to measure GJIC and tumor formation of T47D breast cancer cells. PQ7 at 500 nM induced a 16-fold increase in the GJIC in T47D cells. In addition to an increase in GJIC, a 50% decrease of colony growth was observed with 100 nM of PQ7. PQ7-treated nu/nu mice showed a 100% regression of xenograft tumor growth of T47D cells. The results show that PQ7 has a promising role in exerting anti-tumor activity in human breast cancer cells.

摘要

癌细胞的细胞间隙连接通讯(GJIC)能力降低。增强 GJIC 是减少癌细胞生长的一种可行方法。本报告显示,第二代取代喹啉 PQ7 具有抗肿瘤作用。通过划痕负荷/染料转移和集落生长实验来测量 T47D 乳腺癌细胞的 GJIC 和肿瘤形成。500 nM 的 PQ7 诱导 T47D 细胞中的 GJIC 增加 16 倍。除了 GJIC 增加外,用 100 nM 的 PQ7 观察到集落生长减少 50%。PQ7 处理的 nu/nu 小鼠显示 T47D 细胞的异种移植物肿瘤生长完全消退。结果表明,PQ7 在发挥人类乳腺癌细胞的抗肿瘤活性方面具有广阔的前景。

相似文献

1
Second-generation substituted quinolines as anticancer drugs for breast cancer.第二代取代喹啉类化合物作为乳腺癌的抗癌药物。
Anticancer Res. 2010 Oct;30(10):3927-32.
2
Anti-breast cancer agents, quinolines, targeting gap junction.抗乳腺癌药物,喹啉类,作用于缝隙连接。
Med Chem. 2011 Sep;7(5):448-53. doi: 10.2174/157340611796799131.
3
[Effects of lovastatin on proliferation and gap junctional intercellular communication of human breast cancer cell MCF-7].洛伐他汀对人乳腺癌细胞MCF-7增殖及间隙连接细胞间通讯的影响
Ai Zheng. 2003 Mar;22(3):257-61.
4
[Research on the gap junctional intercellular communication of CHL cells and human cancer cells induced by c9, t11-conjugated linoleic acid].[9,11-共轭亚油酸诱导的CHL细胞与人癌细胞的间隙连接细胞间通讯研究]
Wei Sheng Yan Jiu. 2003 Mar;32(2):113-6.
5
[Studies on the gap junctional intercellular communication (GJIC) of human stomach carcinoma cells in comparison with normal cells and the effect of the tumor promoter, TPA].[人胃癌细胞与正常细胞的间隙连接细胞间通讯(GJIC)研究及肿瘤促进剂佛波酯(TPA)的作用]
Shi Yan Sheng Wu Xue Bao. 1989 Jun;22(2):157-67.
6
Genistein and quercetin increase connexin43 and suppress growth of breast cancer cells.染料木黄酮和槲皮素可增加连接蛋白43的表达并抑制乳腺癌细胞的生长。
Carcinogenesis. 2007 Jan;28(1):93-100. doi: 10.1093/carcin/bgl106. Epub 2006 Jun 15.
7
Potent inhibition of gap junctional intercellular communication by 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) in BALB/c 3T3 cells.3-氯-4-(二氯甲基)-5-羟基-2(5H)-呋喃酮(MX)对BALB/c 3T3细胞间隙连接细胞间通讯的强效抑制作用
Toxicol Lett. 2004 Aug 1;151(3):439-49. doi: 10.1016/j.toxlet.2004.03.012.
8
[Effects of glycidyl methacrylate on gap junctional intercellular communication].甲基丙烯酸缩水甘油酯对间隙连接细胞间通讯的影响
Wei Sheng Yan Jiu. 2000 Mar 30;29(2):73-5.
9
Differential effect of subcellular localization of communication impairing gap junction protein connexin43 on tumor cell growth in vivo.通讯受损的缝隙连接蛋白连接蛋白43亚细胞定位对体内肿瘤细胞生长的差异影响。
Oncogene. 2000 Jan 27;19(4):505-13. doi: 10.1038/sj.onc.1203340.
10
Anticancer activity of litchi fruit pericarp extract against human breast cancer in vitro and in vivo.荔枝果皮提取物对人乳腺癌的体内外抗癌活性
Toxicol Appl Pharmacol. 2006 Sep 1;215(2):168-78. doi: 10.1016/j.taap.2006.02.004. Epub 2006 Mar 23.

引用本文的文献

1
Quinoline as a Privileged Structure: A Recent Update on Synthesis and Biological Activities.喹啉作为一种优势结构:合成与生物活性的最新研究进展。
Curr Top Med Chem. 2024;24(27):2377-2419. doi: 10.2174/0115680266314303240830074056.
2
Synthesis, Docking, and Machine Learning Studies of Some Novel Quinolinesulfonamides-Triazole Hybrids with Anticancer Activity.具有抗癌活性的一些新型喹啉磺胺-三唑杂合体的合成、对接和机器学习研究。
Molecules. 2024 Jul 2;29(13):3158. doi: 10.3390/molecules29133158.
3
An efficient and green synthesis of ferrocenyl-quinoline conjugates a TsOH-catalyzed three-component reaction in water.
一种高效绿色的二茂铁基喹啉共轭物的合成——水相中对甲苯磺酸催化的三组分反应。
RSC Adv. 2018 Mar 6;8(17):9555-9563. doi: 10.1039/c8ra01004h. eCollection 2018 Feb 28.
4
Communication in the Cancer Microenvironment as a Target for Therapeutic Interventions.癌症微环境中的通讯作为治疗干预的靶点
Cancers (Basel). 2020 May 14;12(5):1232. doi: 10.3390/cancers12051232.
5
Facile Synthesis and Photophysical Characterization of New Quinoline Dyes.新型喹啉染料的简便合成与光物理表征
J Fluoresc. 2017 Jan;27(1):271-280. doi: 10.1007/s10895-016-1954-5. Epub 2016 Oct 27.
6
Induction of Apoptosis by PQ1, a Gap Junction Enhancer that Upregulates Connexin 43 and Activates the MAPK Signaling Pathway in Mammary Carcinoma Cells.PQ1诱导乳腺癌细胞凋亡,PQ1是一种间隙连接增强剂,可上调连接蛋白43并激活丝裂原活化蛋白激酶信号通路。
Int J Mol Sci. 2016 Jan 29;17(2):178. doi: 10.3390/ijms17020178.
7
Increased expression of CX43 on stromal cells promotes leukemia apoptosis.基质细胞上CX43表达增加促进白血病细胞凋亡。
Oncotarget. 2015 Dec 29;6(42):44323-31. doi: 10.18632/oncotarget.6249.
8
The anticancer effect of PQ1 in the MMTV-PyVT mouse model.PQ1 在 MMTV-PyVT 小鼠模型中的抗癌作用。
Int J Cancer. 2014 Mar 15;134(6):1474-83. doi: 10.1002/ijc.28461. Epub 2013 Sep 19.
9
Bioavailability and efficacy of a gap junction enhancer (PQ7) in a mouse mammary tumor model.间隙连接增强剂(PQ7)在小鼠乳腺肿瘤模型中的生物利用度和疗效。
PLoS One. 2013 Jun 12;8(6):e67174. doi: 10.1371/journal.pone.0067174. Print 2013.
10
Design, synthesis, and evaluation of bioactive small molecules.设计、合成与生物活性小分子的评估。
Chem Rec. 2013 Feb;13(1):60-9. doi: 10.1002/tcr.201200016. Epub 2012 Dec 20.