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本文引用的文献

1
Recent developments in microfluidics for cell studies.微流控技术在细胞研究中的最新进展。
Adv Mater. 2014 Aug 20;26(31):5525-32. doi: 10.1002/adma.201305348. Epub 2014 Feb 17.
2
Mesenchymal-mode migration assay and antimetastatic drug screening with high-throughput microfluidic channel networks.采用高通量微流控通道网络进行间质模式迁移分析和抗转移药物筛选。
Angew Chem Int Ed Engl. 2014 Feb 24;53(9):2344-8. doi: 10.1002/anie.201309885. Epub 2014 Jan 29.
3
MSN anti-cancer nanomedicines: chemotherapy enhancement, overcoming of drug resistance, and metastasis inhibition.MSN 抗癌纳米药物:增强化疗效果、克服耐药性和抑制转移。
Adv Mater. 2014 Jan 22;26(3):391-411. doi: 10.1002/adma.201303123. Epub 2013 Oct 20.
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Cell spreading as a hydrodynamic process.细胞铺展作为一种流体动力学过程。
Soft Matter. 2010 Aug 10;6:4788-4799. doi: 10.1039/c0sm00252.
5
Hypoxia induces a phase transition within a kinase signaling network in cancer cells.缺氧诱导癌细胞中激酶信号网络的相变。
Proc Natl Acad Sci U S A. 2013 Apr 9;110(15):E1352-60. doi: 10.1073/pnas.1303060110. Epub 2013 Mar 25.
6
Strengthened glycolysis under hypoxia supports tumor symbiosis and hexosamine biosynthesis in pancreatic adenocarcinoma.缺氧条件下增强的糖酵解支持胰腺腺癌中的肿瘤共生和己糖胺生物合成。
Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):3919-24. doi: 10.1073/pnas.1219555110. Epub 2013 Feb 13.
7
Hypoxia stimulates migration of breast cancer cells via the PERK/ATF4/LAMP3-arm of the unfolded protein response.缺氧通过未折叠蛋白反应的PERK/ATF4/LAMP3途径刺激乳腺癌细胞迁移。
Breast Cancer Res. 2013 Jan 7;15(1):R2. doi: 10.1186/bcr3373.
8
Migration of cells in a social context.细胞在社会环境中的迁移。
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9
Microfluidics separation reveals the stem-cell-like deformability of tumor-initiating cells.微流控分离揭示了肿瘤起始细胞的干细胞样变形能力。
Proc Natl Acad Sci U S A. 2012 Nov 13;109(46):18707-12. doi: 10.1073/pnas.1209893109. Epub 2012 Oct 29.
10
Multiple biological activities of lactic acid in cancer: influences on tumor growth, angiogenesis and metastasis.乳酸在癌症中的多种生物学活性:对肿瘤生长、血管生成和转移的影响。
Curr Pharm Des. 2012;18(10):1319-30. doi: 10.2174/138161212799504902.

利用高通量微流控平台研究缺氧驱动的间充质模式细胞迁移。

Utilizing a high-throughput microfluidic platform to study hypoxia-driven mesenchymal-mode cell migration.

作者信息

Zhang Yuanqing, Wen Jianguo, Zhou Ledu, Qin Lidong

机构信息

Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.

出版信息

Integr Biol (Camb). 2015 Jun;7(6):672-80. doi: 10.1039/c5ib00059a. Epub 2015 May 12.

DOI:10.1039/c5ib00059a
PMID:25965948
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4476408/
Abstract

Hypoxia is a critical microenvironment in tumor pathogenesis. There is a close relationship between hypoxia, tumor metastasis and poor prognosis. Hypoxia has been shown to induce epithelial-mesenchymal transition and high levels of lactic acid production, through which cancer cells gain migratory capability. Here, we present a high-throughput microfluidic platform with a controlled oxygen environment to specifically monitor mesenchymal migration under hypoxic conditions. We found that, combined with a slightly alkaline microenvironment, such a platform can help to improve the efficiency of antimetastatic drugs. We also use this platform to study primary and rare cells from mice and demonstrate the correlation between on-chip results and in vivo outcome. This device may provide a new opportunity for biologists and clinicians to better perform assays that evaluate cancer cell behaviors related to metastasis.

摘要

缺氧是肿瘤发病机制中的关键微环境。缺氧与肿瘤转移及不良预后密切相关。研究表明,缺氧可诱导上皮-间质转化并产生高水平乳酸,癌细胞借此获得迁移能力。在此,我们展示了一种具有可控氧环境的高通量微流控平台,用于特异性监测缺氧条件下的间质迁移。我们发现,结合微碱性微环境,这样的平台有助于提高抗转移药物的效率。我们还利用该平台研究来自小鼠的原代细胞和稀有细胞,并证明芯片上的结果与体内结果之间的相关性。该装置可能为生物学家和临床医生更好地开展评估与转移相关的癌细胞行为的检测提供新机会。