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The Tumor Microenvironment

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Cover of 'The Tumor Microenvironment'

Table of Contents

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    Book Overview
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    Chapter 1 Methods of Immunohistochemistry and Immunofluorescence: Converting Invisible to Visible.
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    Chapter 2 Laser Capture Microdissection as a Tool to Study Tumor Stroma.
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    Chapter 3 Quantitative Analysis of Human Cancer Cell Extravasation Using Intravital Imaging.
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    Chapter 4 Studies on the Tumor Vasculature and Coagulant Microenvironment.
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    Chapter 5 A Microfluidic Method to Mimic Luminal Structures in the Tumor Microenvironment.
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    Chapter 6 Measuring Vascular Permeability In Vivo.
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    Chapter 7 The Tumor Microenvironment
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    Chapter 8 Analyzing the Tumor Microenvironment by Flow Cytometry.
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    Chapter 9 The Tumor Microenvironment
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    Chapter 10 Purification of Immune Cell Populations from Freshly Isolated Murine Tumors and Organs by Consecutive Magnetic Cell Sorting and Multi-parameter Flow Cytometry-Based Sorting.
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    Chapter 11 Viral Engineering of Chimeric Antigen Receptor Expression on Murine and Human T Lymphocytes.
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    Chapter 12 The Tumor Microenvironment
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    Chapter 13 Isolation and Characterization of Low- vs. High-Density Neutrophils in Cancer.
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    Chapter 14 Analysis of Extracellular Vesicles in the Tumor Microenvironment.
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    Chapter 15 Visualizing the Tumor Microenvironment of Liver Metastasis by Spinning Disk Confocal Microscopy.
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    Chapter 16 Intravital Microscopy for Imaging the Tumor Microenvironment in Live Mice.
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    Chapter 17 The Tumor Microenvironment
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    Chapter 18 The Tumor Microenvironment
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    Chapter 19 CRISPR/Cas9 Genome Editing as a Strategy to Study the Tumor Microenvironment in Transgenic Mice.
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    Chapter 20 The Tumor Microenvironment
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    Chapter 21 The Tumor Microenvironment
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    Chapter 22 RNA-Seq as a Tool to Study the Tumor Microenvironment.
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    Chapter 23 Sample Preparation for Mass Spectrometry Analysis of Protein-Protein Interactions in Cancer Cell Lines and Tissues.
Attention for Chapter 3: Quantitative Analysis of Human Cancer Cell Extravasation Using Intravital Imaging.
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Chapter title
Quantitative Analysis of Human Cancer Cell Extravasation Using Intravital Imaging.
Chapter number 3
Book title
The Tumor Microenvironment
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3801-8_3
Pubmed ID
Book ISBNs
978-1-4939-3799-8, 978-1-4939-3801-8
Authors

Lian Willetts, David Bond, Konstantin Stoletov, John D. Lewis Ph.D., John D. Lewis

Editors

Josie Ursini-Siegel, Nicole Beauchemin

Abstract

Metastasis, or the spread of cancer cells from a primary tumor to distant sites, is the leading cause of cancer-associated death. Metastasis is a complex multi-step process comprised of invasion, intravasation, survival in circulation, extravasation, and formation of metastatic colonies. Currently, in vitro assays are limited in their ability to investigate these intricate processes and do not faithfully reflect metastasis as it occurs in vivo. Traditional in vivo models of metastasis are limited by their ability to visualize the seemingly sporadic behavior of where and when cancer cells spread (Reymond et al., Nat Rev Cancer 13:858-870, 2013). The avian embryo model of metastasis is a powerful platform to study many of the critical steps in the metastatic cascade including the migration, extravasation, and invasion of human cancer cells in vivo (Sung et al., Nat Commun 6:7164, 2015; Leong et al., Cell Rep 8, 1558-1570, 2014; Kain et al., Dev Dyn 243:216-28, 2014; Leong et al., Nat Protoc 5:1406-17, 2010; Zijlstra et al., Cancer Cell 13:221-234, 2008; Palmer et al., J Vis Exp 51:2815, 2011). The chicken chorioallantoic membrane (CAM) is a readily accessible and well-vascularized tissue that surrounds the developing embryo. When the chicken embryo is grown in a shell-less, ex ovo environment, the nearly transparent CAM provides an ideal environment for high-resolution fluorescent microcopy approaches. In this model, the embryonic chicken vasculature and labeled cancer cells can be visualized simultaneously to investigate specific steps in the metastatic cascade including extravasation. When combined with the proper image analysis tools, the ex ovo chicken embryo model offers a cost-effective and high-throughput platform for the quantitative analysis of tumor cell metastasis in a physiologically relevant in vivo setting. Here we discuss detailed procedures to quantify cancer cell extravasation in the shell-less chicken embryo model with advanced fluorescence microscopy techniques.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 18%
Student > Ph. D. Student 2 18%
Student > Doctoral Student 1 9%
Professor 1 9%
Researcher 1 9%
Other 1 9%
Unknown 3 27%
Readers by discipline Count As %
Medicine and Dentistry 4 36%
Arts and Humanities 1 9%
Veterinary Science and Veterinary Medicine 1 9%
Biochemistry, Genetics and Molecular Biology 1 9%
Engineering 1 9%
Other 0 0%
Unknown 3 27%