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本文引用的文献

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Setup and use of a two-laser multiphoton microscope for multichannel intravital fluorescence imaging.建立和使用双激光多光子显微镜进行多通道活细胞荧光成像。
Nat Protoc. 2011 Sep 8;6(10):1500-20. doi: 10.1038/nprot.2011.376.
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Mena invasive (MenaINV) promotes multicellular streaming motility and transendothelial migration in a mouse model of breast cancer.Mena 入侵(MenaINV)促进乳腺癌小鼠模型中的多细胞流动力和跨内皮迁移。
J Cell Sci. 2011 Jul 1;124(Pt 13):2120-31. doi: 10.1242/jcs.086231.
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Mena invasive (Mena(INV)) and Mena11a isoforms play distinct roles in breast cancer cell cohesion and association with TMEM.Mena 侵袭(Mena(INV))和 Mena11a 异构体在乳腺癌细胞黏附和与 TMEM 相关联方面发挥不同的作用。
Clin Exp Metastasis. 2011 Aug;28(6):515-27. doi: 10.1007/s10585-011-9388-6. Epub 2011 Apr 12.
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A novel spatiotemporal RhoC activation pathway locally regulates cofilin activity at invadopodia.一种新的时空 RhoC 激活途径局部调节侵袭伪足处的肌动蛋白丝解聚因子的活性。
Curr Biol. 2011 Apr 26;21(8):635-44. doi: 10.1016/j.cub.2011.03.039. Epub 2011 Apr 7.
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Efficient generation of gene knockout plasmids for Dictyostelium discoideum using one-step cloning.一步克隆法高效生成基因敲除质粒用于盘基网柄菌。
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An EGFR-Src-Arg-cortactin pathway mediates functional maturation of invadopodia and breast cancer cell invasion.EGFR-Src-Arg-cortactin 通路介导侵袭伪足的功能成熟和乳腺癌细胞侵袭。
Cancer Res. 2011 Mar 1;71(5):1730-41. doi: 10.1158/0008-5472.CAN-10-1432. Epub 2011 Jan 21.
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mTORC2 regulates neutrophil chemotaxis in a cAMP- and RhoA-dependent fashion.mTORC2 通过 cAMP 和 RhoA 依赖的方式调节中性粒细胞趋化性。
Dev Cell. 2010 Dec 14;19(6):845-57. doi: 10.1016/j.devcel.2010.11.004.
8
Mena deficiency delays tumor progression and decreases metastasis in polyoma middle-T transgenic mouse mammary tumors.Mena 缺乏可延迟多瘤病毒中 T 抗原转基因鼠乳腺肿瘤的进展并减少转移。
Breast Cancer Res. 2010;12(6):R101. doi: 10.1186/bcr2784. Epub 2010 Nov 25.
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Does tumour dormancy offer a therapeutic target?肿瘤休眠是否提供了治疗靶点?
Nat Rev Cancer. 2010 Dec;10(12):871-7. doi: 10.1038/nrc2933. Epub 2010 Nov 4.
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An arrayed high-content chemotaxis assay for patient diagnosis.用于患者诊断的高通量高内涵化学趋药性分析检测法。
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癌症中的趋化作用。

Chemotaxis in cancer.

机构信息

Department of Anatomy and Structural Biology, Program in Tumor Microenvironment and Metastasis, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York 10461, USA.

出版信息

Nat Rev Cancer. 2011 Jul 22;11(8):573-87. doi: 10.1038/nrc3078.

DOI:10.1038/nrc3078
PMID:21779009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4030706/
Abstract

Chemotaxis of tumour cells and stromal cells in the surrounding microenvironment is an essential component of tumour dissemination during progression and metastasis. This Review summarizes how chemotaxis directs the different behaviours of tumour cells and stromal cells in vivo, how molecular pathways regulate chemotaxis in tumour cells and how chemotaxis choreographs cell behaviour to shape the tumour microenvironment and to determine metastatic spread. The central importance of chemotaxis in cancer progression is highlighted by discussion of the use of chemotaxis as a prognostic marker, a treatment end point and a target of therapeutic intervention.

摘要

肿瘤细胞和周围微环境中的基质细胞的趋化作用是肿瘤进展和转移过程中肿瘤扩散的一个重要组成部分。本综述总结了趋化作用如何指导肿瘤细胞和基质细胞在体内的不同行为,分子途径如何调节肿瘤细胞的趋化作用,以及趋化作用如何编排细胞行为以塑造肿瘤微环境并决定转移扩散。通过讨论趋化作用作为预后标志物、治疗终点和治疗干预靶点,突出了趋化作用在癌症进展中的核心重要性。