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Nanoroughened adhesion-based capture of circulating tumor cells with heterogeneous expression and metastatic characteristics.基于纳米粗糙化粘附捕获具有异质性表达和转移特征的循环肿瘤细胞。
BMC Cancer. 2016 Aug 8;16:614. doi: 10.1186/s12885-016-2638-x.
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YAP/TAZ at the Roots of Cancer.YAP/TAZ与癌症根源
Cancer Cell. 2016 Jun 13;29(6):783-803. doi: 10.1016/j.ccell.2016.05.005.
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Atomic force microscopy indentation and inverse analysis for non-linear viscoelastic identification of breast cancer cells.用于乳腺癌细胞非线性粘弹性识别的原子力显微镜压痕及反演分析
Math Biosci. 2016 Jul;277:77-88. doi: 10.1016/j.mbs.2016.03.015. Epub 2016 Apr 21.
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Multiparametric Biomechanical and Biochemical Phenotypic Profiling of Single Cancer Cells Using an Elasticity Microcytometer.使用弹性微细胞仪对单个癌细胞进行多参数生物力学和生化表型分析。
Small. 2016 May;12(17):2300-11. doi: 10.1002/smll.201503620. Epub 2016 Mar 1.
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Breast cancer stem cells transition between epithelial and mesenchymal states reflective of their normal counterparts.乳腺癌干细胞在上皮和间充质状态之间转换,反映了它们正常对应物的特征。
Stem Cell Reports. 2013 Dec 27;2(1):78-91. doi: 10.1016/j.stemcr.2013.11.009. eCollection 2014 Jan 14.
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Presence of anaplastic lymphoma kinase in inflammatory breast cancer.炎性乳腺癌中间变性淋巴瘤激酶的存在。
Springerplus. 2013 Oct 1;2:497. doi: 10.1186/2193-1801-2-497. eCollection 2013.
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Acoustic tweezing cytometry for live-cell subcellular modulation of intracellular cytoskeleton contractility.用于活细胞内细胞骨架收缩性亚细胞调控的声镊细胞术
Sci Rep. 2013;3:2176. doi: 10.1038/srep02176.
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Modeling the mechanics of cancer: effect of changes in cellular and extra-cellular mechanical properties.癌症力学建模:细胞和细胞外机械特性变化的影响。
Front Oncol. 2013 Jun 11;3:145. doi: 10.3389/fonc.2013.00145. eCollection 2013.
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Characterizing deformability and surface friction of cancer cells.表征癌细胞的变形性和表面摩擦。
Proc Natl Acad Sci U S A. 2013 May 7;110(19):7580-5. doi: 10.1073/pnas.1218806110. Epub 2013 Apr 22.
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Nanoroughened surfaces for efficient capture of circulating tumor cells without using capture antibodies.纳米粗糙表面可高效捕获循环肿瘤细胞,无需使用捕获抗体。
ACS Nano. 2013 Jan 22;7(1):566-75. doi: 10.1021/nn304719q. Epub 2012 Dec 5.

生物物理表型分析和 ALDH+炎性乳腺癌干细胞样细胞的调控。

Biophysical Phenotyping and Modulation of ALDH+ Inflammatory Breast Cancer Stem-Like Cells.

机构信息

Department of Mechanical and Aerospace Engineering, New York University, Brooklyn, NY, 11201, USA.

Department of Biomedical Engineering, New York University, Brooklyn, NY, 11201, USA.

出版信息

Small. 2019 Feb;15(5):e1802891. doi: 10.1002/smll.201802891. Epub 2019 Jan 11.

DOI:10.1002/smll.201802891
PMID:30632269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6486377/
Abstract

Cancer stem-like cells (CSCs) have been shown to initiate tumorigenesis and cancer metastasis in many cancer types. Although identification of CSCs through specific marker expression helps define the CSC compartment, it does not directly provide information on how or why this cancer cell subpopulation is more metastatic or tumorigenic. In this study, the functional and biophysical characteristics of aggressive and lethal inflammatory breast cancer (IBC) CSCs at the single-cell level are comprehensively profiled using multiple microengineered tools. Distinct functional (cell migration, growth, adhesion, invasion and self-renewal) and biophysical (cell deformability, adhesion strength and contractility) properties of ALDH+ SUM149 IBC CSCs are found as compared to their ALDH- non-CSC counterpart, providing biophysical insights into why CSCs has an enhanced propensity to metastasize. It is further shown that the cellular biophysical phenotype can predict and determine IBC cells' tumorigenic ability. SUM149 and SUM159 IBC cells selected and modulated through biophysical attributes-adhesion and stiffness-show characteristics of CSCs in vitro and enhance tumorigenicity in in vivo murine models of primary tumor growth. Overall, the multiparametric cellular biophysical phenotyping and modulation of IBC CSCs yields a new understanding of IBC's metastatic properties and how they might develop and be targeted for therapeutic interventions.

摘要

癌症干细胞(CSCs)已被证明在多种癌症类型中启动肿瘤发生和癌症转移。虽然通过特定标志物表达鉴定 CSCs 有助于定义 CSC 区室,但它并不能直接提供有关该癌细胞亚群为何更具转移性或致瘤性的信息。在这项研究中,使用多种微工程工具,全面描绘了具有侵袭性和致命性的炎症性乳腺癌(IBC)CSCs 在单细胞水平上的功能和生物物理特性。与 ALDH-非 CSC 对应物相比,ALDH+ SUM149 IBC CSCs 具有明显不同的功能(细胞迁移、生长、粘附、侵袭和自我更新)和生物物理特性(细胞变形性、粘附强度和收缩性),为 CSCs 为何具有更强的转移倾向提供了生物物理见解。进一步表明,细胞生物物理表型可以预测和确定 IBC 细胞的致瘤能力。通过生物物理特性(粘附和刚性)选择和调节的 SUM149 和 SUM159 IBC 细胞在体外表现出 CSCs 的特征,并在体内原发性肿瘤生长的小鼠模型中增强了致瘤性。总体而言,IBC CSCs 的多参数细胞生物物理表型和调节提供了对 IBC 转移特性的新认识,以及它们可能如何发展以及如何针对治疗干预进行靶向。