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本文引用的文献

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Differential response to doxorubicin in breast cancer subtypes simulated by a microfluidic tumor model.微流控肿瘤模型模拟乳腺癌亚型对多柔比星的反应差异。
J Control Release. 2017 Nov 28;266:129-139. doi: 10.1016/j.jconrel.2017.09.024. Epub 2017 Sep 20.
2
Engineered Microvasculature in PDMS Networks Using Endothelial Cells Derived from Human Induced Pluripotent Stem Cells.利用源自人诱导多能干细胞的内皮细胞在 PDMS 网络中构建工程化微血管。
Cell Transplant. 2017 Aug;26(8):1365-1379. doi: 10.1177/0963689717720282.
3
In vitro microfluidic models of tumor microenvironment to screen transport of drugs and nanoparticles.用于筛选药物和纳米颗粒转运的肿瘤微环境体外微流控模型。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2017 Sep;9(5). doi: 10.1002/wnan.1460. Epub 2017 Feb 14.
4
Simulation of complex transport of nanoparticles around a tumor using tumor-microenvironment-on-chip.使用芯片上的肿瘤微环境模拟纳米颗粒在肿瘤周围的复杂运输。
J Control Release. 2014 Nov 28;194:157-67. doi: 10.1016/j.jconrel.2014.08.027. Epub 2014 Sep 3.
5
In vivo optical imaging of cancer metastasis using multiphoton microscopy: a short review.使用多光子显微镜对癌症转移进行的体内光学成像:简短综述。
Am J Transl Res. 2014 May 15;6(3):179-87. eCollection 2014.
6
A microfluidic 3D in vitro model for specificity of breast cancer metastasis to bone.用于研究乳腺癌骨转移特异性的微流控 3D 体外模型。
Biomaterials. 2014 Mar;35(8):2454-61. doi: 10.1016/j.biomaterials.2013.11.050. Epub 2013 Dec 31.
7
Crossing the endothelial barrier during metastasis.在转移过程中穿过内皮屏障。
Nat Rev Cancer. 2013 Dec;13(12):858-70. doi: 10.1038/nrc3628.
8
Definition of molecular determinants of prostate cancer cell bone extravasation.前列腺癌细胞骨外渗的分子决定因素的定义。
Cancer Res. 2013 Jan 15;73(2):942-52. doi: 10.1158/0008-5472.CAN-12-3264. Epub 2012 Nov 13.
9
Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.Cdc42 通过β1 整合素促进癌细胞的跨内皮迁移。
J Cell Biol. 2012 Nov 12;199(4):653-68. doi: 10.1083/jcb.201205169.
10
Microfluidic models of vascular functions.血管功能的微流控模型。
Annu Rev Biomed Eng. 2012;14:205-30. doi: 10.1146/annurev-bioeng-071811-150052. Epub 2012 Apr 23.

使用微流控平台分析癌细胞在炎症内皮上的黏附动力学。

Analysis of adhesion kinetics of cancer cells on inflamed endothelium using a microfluidic platform.

作者信息

Thompson Taylor J, Han Bumsoo

机构信息

School of Mechanical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

Biomicrofluidics. 2018 Jun 8;12(4):042215. doi: 10.1063/1.5025891. eCollection 2018 Jul.

DOI:10.1063/1.5025891
PMID:29937953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5993669/
Abstract

Metastasis is the ultimate cause of death among the vast majority of cancer patients. This process is comprised of multiple steps, including the migration of circulating cancer cells across microvasculature. This trans-endothelial migration involves the adhesion and eventual penetration of cancer cells to the vasculature of the target organ. Many of these mechanisms remain poorly understood due to poor control of pathophysiological conditions in tumor models. In this work, a microfluidic device was developed to support the culture and observation of engineered microvasculature with systematic control of the environmental characteristics. This device was then used to study the adhesion of circulating cancer cells to an endothelium under varying conditions to delineate the effects of hemodynamics and inflammations. The resulting understanding will help to establish a quantitative and biophysical mechanism of interactions between cancer cells and endothelium.

摘要

转移是绝大多数癌症患者死亡的最终原因。这个过程由多个步骤组成,包括循环癌细胞穿过微血管的迁移。这种跨内皮迁移涉及癌细胞与靶器官血管的黏附及最终穿透。由于肿瘤模型中病理生理条件控制不佳,许多这些机制仍知之甚少。在这项工作中,开发了一种微流控装置,以在系统控制环境特征的情况下支持工程化微血管的培养和观察。然后使用该装置研究循环癌细胞在不同条件下与内皮的黏附,以阐明血流动力学和炎症的影响。由此获得的认识将有助于建立癌细胞与内皮之间相互作用的定量和生物物理机制。