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Proteases and Cancer

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Cover of 'Proteases and Cancer'

Table of Contents

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    Book Overview
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    Chapter 1 Dissecting Degradomes: Analysis of Protease-Coding Genes
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    Chapter 2 Identification of Protease Cleavage Sites and Substrates in Cancer by Carboxy-TAILS (C-TAILS)
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    Chapter 3 Identification of Proteolytic Cleavage Sites of EphA2 by Membrane Type 1 Matrix Metalloproteinase on the Surface of Cancer Cells
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    Chapter 4 Biotin-Chasing Assay to Evaluate uPAR Stability and Cleavage on the Surface of Cells
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    Chapter 5 Determination of Aconitase Activity: A Substrate of the Mitochondrial Lon Protease
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    Chapter 6 A Simple Cell-Based Assay for the Detection of Surface Protein Shedding by Rhomboid Proteases
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    Chapter 7 Functional Production of Catalytic Domains of Human MMPs in Escherichia coli Periplasm
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    Chapter 8 Autophagy and Proteases: Basic Study of the Autophagic Flux by Western Blot
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    Chapter 9 Gel-Based Gelatin Zymography to Examine Matrix Metalloproteinase Activity in Cell Culture
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    Chapter 10 Analysis of Enzymatic Activity of Matrix Metalloproteinase (MMP) by Collagen Zymography in Melanoma
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    Chapter 11 Measurement of Protease Activities Using Fluorogenic Substrates
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    Chapter 12 Targeting the Expression of Cathepsin B Using CRISPR/Cas9 System in Mammalian Cancer Cells
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    Chapter 13 Assessing the Influence of a Protease in Cell Migration Using the Barrier-Migration Assay
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    Chapter 14 Analysis of Invasive Activity of CAF Spheroids into Three Dimensional (3D) Collagen Matrices
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    Chapter 15 Beyond the Proteolytic Activity: Examining the Functional Relevance of the Ancillary Domains Using Tri-Dimensional (3D) Spheroid Invasion Assay
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    Chapter 16 Analyzing the Type II Transmembrane Serine Protease Hepsin-Dependent Basement Membrane Remodeling in 3D Cell Culture
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    Chapter 17 Evaluation of Tumor Vasculature Using a Syngeneic Tumor Model in Wild-Type and Genetically Modified Mice
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    Chapter 18 3D Image Analysis of the Microvasculature in Healthy and Diseased Tissues
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    Chapter 19 Human Tumor Tissue-Based 3D In Vitro Invasion Assays
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    Chapter 20 Ear Sponge Assay: A Method to Investigate Angiogenesis and Lymphangiogenesis in Mice
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    Chapter 21 Cancer Susceptibility Models in Protease-Deficient Mice
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    Chapter 22 Imaging Proteolytic Activities in Mouse Models of Cancer
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    Chapter 23 Protease Silencing to Explore the Molecular Mechanisms of Cancer and Aging
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    Chapter 24 Analysis of Somatic DNA Methylation Alterations of Genes Encoding Cell Surface Metallopeptidases in Colorectal Cancer
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    Chapter 25 Targeting Deubiquitinases in Cancer
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    Chapter 26 Generation of Highly Selective MMP Antibody Inhibitors
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    Chapter 27 Strategies to Target Matrix Metalloproteinases as Therapeutic Approach in Cancer
Attention for Chapter 13: Assessing the Influence of a Protease in Cell Migration Using the Barrier-Migration Assay
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Chapter title
Assessing the Influence of a Protease in Cell Migration Using the Barrier-Migration Assay
Chapter number 13
Book title
Proteases and Cancer
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7595-2_13
Pubmed ID
Book ISBNs
978-1-4939-7594-5, 978-1-4939-7595-2
Authors

Tania Fontanil, Yamina Mohamedi, Santiago Cal, Álvaro J. Obaya

Abstract

Proteases play crucial roles in all steps of tumor progression including cancer cell migration. In fact, uncontrolled proteolytic activity could lead to the degradation of different components of the extracellular matrix which facilitates dissemination of tumor cells. However, numerous studies have revealed that proteases may also exert tumor-protective actions which could impede progression of malignant cells. Consequently, it is crucial to distinguish those situations in which proteases promote tumor growth from those in which exhibit tumor-suppressive effects. In this regard, analysis of the influence of a particular protease on the capacity of a cell line to migrate can be employed as an approach to better understand its involvement in tumorigenesis. Different experimental designs have been developed to investigate cell migration. Herein, we describe a barrier assay to monitor cell migration, which overcomes some disadvantages of traditional methods such as the Boyden chamber or the wound healing assays. The version of the barrier assay explained in this chapter allows to examine cell migration through the analysis of the closure of a premade 500 μm wound. This method also facilitates comparison between two different situations in a given cell line (i.e., gene up- or downregulation) in the same assay and under the same conditions. Additionally, migration can be monitored and measured using a time lapse microscope which facilitates further analysis through different softwares.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Other 1 33%
Unknown 2 67%
Readers by discipline Count As %
Computer Science 1 33%
Unknown 2 67%