• 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

相似文献

1
Rebuilding cancer metastasis in the mouse.在小鼠中重建癌症转移。
Mol Oncol. 2013 Apr;7(2):283-96. doi: 10.1016/j.molonc.2013.02.009. Epub 2013 Feb 20.
2
Mouse models of metastasis: progress and prospects.转移的小鼠模型:进展与展望。
Dis Model Mech. 2017 Sep 1;10(9):1061-1074. doi: 10.1242/dmm.030403.
3
Epithelial-mesenchymal plasticity is a decisive feature for the metastatic outgrowth of disseminated WAP-T mouse mammary carcinoma cells.上皮-间质可塑性是播散的WAP-T小鼠乳腺癌细胞转移生长的决定性特征。
BMC Cancer. 2015 Mar 26;15:178. doi: 10.1186/s12885-015-1165-5.
4
Modeling metastasis in the mouse.在小鼠中建立转移模型。
Curr Opin Pharmacol. 2010 Oct;10(5):571-7. doi: 10.1016/j.coph.2010.06.003. Epub 2010 Jul 1.
5
Metastasis suppression by adiponectin: LKB1 rises up to the challenge.脂联素抑制转移:LKB1 迎难而上。
Cell Adh Migr. 2010 Jul-Sep;4(3):358-62. doi: 10.4161/cam.4.3.11541. Epub 2010 Jul 17.
6
Mouse Models of Metastasis and Dormancy.转移和休眠的小鼠模型。
Cold Spring Harb Perspect Med. 2024 Aug 1;14(8):a041386. doi: 10.1101/cshperspect.a041386.
7
SCID-hu mice for the study of human cancer metastasis.用于人类癌症转移研究的重症联合免疫缺陷-人源化小鼠。
Cancer Chemother Pharmacol. 1999;43 Suppl:S37-41. doi: 10.1007/s002800051096.
8
Modeling metastatic breast cancer in mice.在小鼠中模拟转移性乳腺癌。
J Mammary Gland Biol Neoplasia. 2007 Sep;12(2-3):191-203. doi: 10.1007/s10911-007-9050-8.
9
Spontaneous and experimental metastasis models: nude mice.自发和实验性转移模型:裸鼠。
Methods Mol Biol. 2014;1070:223-33. doi: 10.1007/978-1-4614-8244-4_17.
10
Metastatic cancer cells with macrophage properties: evidence from a new murine tumor model.具有巨噬细胞特性的转移性癌细胞:来自一种新型小鼠肿瘤模型的证据。
Int J Cancer. 2008 Jul 1;123(1):73-84. doi: 10.1002/ijc.23492.

引用本文的文献

1
Establishment of an Orthotopic and Metastatic Colorectal Cancer Mouse Model Using a Tissue Adhesive-Based Implantation Method.使用基于组织粘合剂的植入方法建立原位和转移性结直肠癌小鼠模型
Cancers (Basel). 2025 Jul 7;17(13):2266. doi: 10.3390/cancers17132266.
2
Biological profile of breast cancer brain metastasis.乳腺癌脑转移的生物学特征。
Acta Neuropathol Commun. 2025 Apr 19;13(1):78. doi: 10.1186/s40478-025-01983-4.
3
A Review of Talin- and Integrin-Dependent Molecular Mechanisms in Cancer Invasion and Metastasis.关于癌症侵袭和转移中依赖于踝蛋白和整合素的分子机制的综述。
Int J Mol Sci. 2025 Feb 20;26(5):1798. doi: 10.3390/ijms26051798.
4
Multiplex, high-throughput method to study cancer and immune cell mechanotransduction.用于研究癌症和免疫细胞力学转导的多重、高通量方法。
Commun Biol. 2024 Jun 1;7(1):674. doi: 10.1038/s42003-024-06327-x.
5
Compromised Blood-Brain Barrier Junctions Enhance Melanoma Cell Intercalation and Extravasation.受损的血脑屏障连接增强黑色素瘤细胞的嵌入和外渗。
Cancers (Basel). 2023 Oct 20;15(20):5071. doi: 10.3390/cancers15205071.
6
Nanotechnology-Aided Advancement in Combating the Cancer Metastasis.纳米技术助力对抗癌症转移的进展
Pharmaceuticals (Basel). 2023 Jun 19;16(6):899. doi: 10.3390/ph16060899.
7
Investigating the Role of Heparanase in Breast Cancer Development Utilising the MMTV-PyMT Murine Model of Mammary Carcinoma.利用MMTV-PyMT小鼠乳腺癌模型研究乙酰肝素酶在乳腺癌发展中的作用。
Cancers (Basel). 2023 Jun 5;15(11):3062. doi: 10.3390/cancers15113062.
8
miR-1246 in tumor extracellular vesicles promotes metastasis increased tumor cell adhesion and endothelial cell barrier destruction.肿瘤细胞外囊泡中的miR-1246促进转移,增加肿瘤细胞黏附并破坏内皮细胞屏障。
Front Oncol. 2023 Apr 12;13:973871. doi: 10.3389/fonc.2023.973871. eCollection 2023.
9
The Chemotherapeutic Efficacy of Hyaluronic Acid Coated Polymeric Nanoparticles against Breast Cancer Metastasis in Female NCr-Nu/Nu Nude Mice.透明质酸包被的聚合物纳米颗粒对雌性NCr-Nu/Nu裸鼠乳腺癌转移的化疗疗效
Polymers (Basel). 2023 Jan 5;15(2):284. doi: 10.3390/polym15020284.
10
A Tumor Accelerator Based on Multicomponent Bone Scaffolds and Cancer Cell Homing.基于多组分骨支架和癌细胞归巢的肿瘤加速器
Polymers (Basel). 2022 Aug 16;14(16):3340. doi: 10.3390/polym14163340.

本文引用的文献

1
Chick chorioallantoic membrane (CAM) assay as an in vivo model to study the effect of newly identified molecules on ovarian cancer invasion and metastasis.鸡胚绒毛尿囊膜(CAM)试验作为一种体内模型,用于研究新鉴定分子对卵巢癌侵袭和转移的影响。
Int J Mol Sci. 2012;13(8):9959-9970. doi: 10.3390/ijms13089959. Epub 2012 Aug 10.
2
Role of wild type p53 and double suicide genes in interventional therapy of liver cancer in rabbits.野生型p53和双自杀基因在兔肝癌介入治疗中的作用
Acta Cir Bras. 2012 Aug;27(8):522-8. doi: 10.1590/s0102-86502012000800002.
3
[Not Available].[无可用内容]。
Drug Discov Today Dis Models. 2011 Fall;8(2-3):67-74. doi: 10.1016/j.ddmod.2011.05.003. Epub 2011 Jul 1.
4
Unravelling the complexity of metastasis - molecular understanding and targeted therapies.解析转移的复杂性 - 分子理解和靶向治疗。
Nat Rev Cancer. 2011 Sep 23;11(10):735-48. doi: 10.1038/nrc3125.
5
The influence of removal of primary tumor on incidence and phenotype of circulating tumor cells in primary breast cancer.原发肿瘤切除对原发性乳腺癌循环肿瘤细胞发生率和表型的影响。
Breast Cancer Res Treat. 2012 Feb;132(1):121-9. doi: 10.1007/s10549-011-1569-0. Epub 2011 May 12.
6
Loss of PI3K blocks cell-cycle progression in a Drosophila tumor model.PI3K 的缺失会阻止果蝇肿瘤模型中的细胞周期进程。
Oncogene. 2011 Sep 29;30(39):4067-74. doi: 10.1038/onc.2011.125. Epub 2011 Apr 25.
7
A perspective on cancer cell metastasis.癌症细胞转移的观点。
Science. 2011 Mar 25;331(6024):1559-64. doi: 10.1126/science.1203543.
8
Hallmarks of cancer: the next generation.癌症的特征:下一代。
Cell. 2011 Mar 4;144(5):646-74. doi: 10.1016/j.cell.2011.02.013.
9
SMAD4-dependent barrier constrains prostate cancer growth and metastatic progression.SMAD4 依赖性屏障限制前列腺癌生长和转移进展。
Nature. 2011 Feb 10;470(7333):269-73. doi: 10.1038/nature09677. Epub 2011 Feb 2.
10
How genetically engineered mouse tumor models provide insights into human cancers.基因工程小鼠肿瘤模型如何为人类癌症提供深入了解。
J Clin Oncol. 2011 Jun 1;29(16):2273-81. doi: 10.1200/JCO.2010.30.8304. Epub 2011 Jan 24.

在小鼠中重建癌症转移。

Rebuilding cancer metastasis in the mouse.

机构信息

Department of Biomedicine, University of Basel, Mattenstrasse 28, 4058 Basel, Switzerland.

出版信息

Mol Oncol. 2013 Apr;7(2):283-96. doi: 10.1016/j.molonc.2013.02.009. Epub 2013 Feb 20.

DOI:10.1016/j.molonc.2013.02.009
PMID:23474222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5528417/
Abstract

Most cancer deaths are due to the systemic dissemination of cancer cells and the formation of secondary tumors (metastasis) in distant organs. Recent years have brought impressive progress in metastasis research, yet we still lack sufficient insights into how cancer cells migrate out of primary tumors and invade into neighboring tissue, intravasate into the blood or the lymphatic circulation, survive in the blood stream, and target specific organs to initiate metastatic outgrowth. While a large number of cellular and animal models of cancer have been crucial in delineating the molecular mechanisms underlying tumor initiation and progression, experimental models that faithfully recapitulate the multiple stages of metastatic disease are still scarce. The advent of sophisticated genetic engineering in mice, in particular the ability to manipulate gene expression in specific tissue and at desired time points at will, have allowed to rebuild the metastatic process in mice. Here, we describe a selection of cellular experimental systems, tumor transplantation mouse models and genetically engineered mouse models that are used for monitoring specific processes involved in metastasis, such as cell migration and invasion, and for investigating the full metastatic process. Such models not only aid in deciphering the pathomechanisms of metastasis, but are also instrumental for the preclinical testing of anti-metastatic therapies and further refinement and generation of improved models.

摘要

大多数癌症死亡是由于癌细胞的系统性扩散以及在远处器官形成继发性肿瘤(转移)。近年来,转移研究取得了令人印象深刻的进展,但我们仍然缺乏足够的了解,即癌细胞如何从原发性肿瘤中迁移出来并侵入邻近组织,进入血液或淋巴循环,在血液中存活,并靶向特定器官引发转移性生长。虽然大量的癌症细胞和动物模型对于阐明肿瘤起始和进展的分子机制至关重要,但仍缺乏能够真实再现转移性疾病多个阶段的实验模型。小鼠中复杂的基因工程的出现,特别是能够随意在特定组织和所需时间点操纵基因表达的能力,使得在小鼠中重建转移过程成为可能。在这里,我们描述了一系列用于监测转移过程中涉及的特定过程(如细胞迁移和侵袭)以及研究完整转移过程的细胞实验系统、肿瘤移植小鼠模型和基因工程小鼠模型。这些模型不仅有助于解析转移的病理机制,而且对于抗转移治疗的临床前测试以及进一步改进和生成改进模型也非常重要。