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Isolation and Molecular Characterization of Circulating Tumor Cells

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Cover of 'Isolation and Molecular Characterization of Circulating Tumor Cells'

Table of Contents

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    Book Overview
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    Chapter 1 Circulating Tumor Cells as Cancer Biomarkers in the Clinic
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    Chapter 2 Strategies for Isolation and Molecular Profiling of Circulating Tumor Cells
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    Chapter 3 Aptamer-Based Methods for Detection of Circulating Tumor Cells and Their Potential for Personalized Diagnostics
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    Chapter 4 Development of a Protocol for Single-Cell Analysis of Circulating Tumor Cells in Patients with Solid Tumors
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    Chapter 5 Flow Cytometric Methods for Circulating Tumor Cell Isolation and Molecular Analysis
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    Chapter 6 Enrichment and Detection of Circulating Tumor Cells and Other Rare Cell Populations by Microfluidic Filtration
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    Chapter 7 Detection and Enumeration of Circulating Tumor Cells with Invasive Phenotype
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    Chapter 8 Molecular Profiling and Significance of Circulating Tumor Cell Based Genetic Signatures
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    Chapter 9 Detection of Gene Rearrangements in Circulating Tumor Cells: Examples of ALK-, ROS1-, RET-Rearrangements in Non-Small-Cell Lung Cancer and ERG-Rearrangements in Prostate Cancer
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    Chapter 10 Enrichment, Isolation and Molecular Characterization of EpCAM-Negative Circulating Tumor Cells
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    Chapter 11 Expression of Epithelial Mesenchymal Transition and Cancer Stem Cell Markers in Circulating Tumor Cells
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    Chapter 12 Mesenchymal-Epithelial Transition and Circulating Tumor Cells in Small Cell Lung Cancer
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    Chapter 13 Clinical Relevance of a Candidate Stem Cell Marker, p75 Neurotrophin Receptor (p75NTR) Expression in Circulating Tumor Cells
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    Chapter 14 Personalized Treatment Through Detection and Monitoring of Genetic Aberrations in Single Circulating Tumor Cells
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    Chapter 15 Glycan Markers as Potential Immunological Targets in Circulating Tumor Cells
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    Chapter 16 Significance of EGFR Expression in Circulating Tumor Cells
Attention for Chapter 16: Significance of EGFR Expression in Circulating Tumor Cells
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Chapter title
Significance of EGFR Expression in Circulating Tumor Cells
Chapter number 16
Book title
Isolation and Molecular Characterization of Circulating Tumor Cells
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-3-319-55947-6_16
Pubmed ID
Book ISBNs
978-3-31-955946-9, 978-3-31-955947-6
Authors

María José Serrano, María Jesús Alvarez-Cubero, Diego De Miguel Pérez, Alba Rodríguez-Martínez, Lucas Gonzalez-Herrera, Inmaculada Robles-Fernandez, José Exposito Hernandez, Jose Luis García Puche, José Antonio Lorente, Serrano, María José, Alvarez-Cubero, María Jesús, De Miguel Pérez, Diego, Rodríguez-Martínez, Alba, Gonzalez-Herrera, Lucas, Robles-Fernandez, Inmaculada, Hernandez, José Exposito, Puche, Jose Luis García, Lorente, José Antonio

Abstract

This chapter focuses on a deep description of the epidermal growth factor receptor (EGFR) expression in circulating tumor cells (CTCs) and its main role in cancer progression, genetic changes related to metastasis , and resistance to treatment. The aberrant behavior of cancer cells is caused by genetic mutations and altered patterns of gene expression. These changes can be responsible for an increase in cell motility but also an ability of CTCs to survival in different microenvironments, as well as developing therapy-resistant clones. Finally, CTCs can acquire the ability to invade distant organs, where metastatic foci can develop.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 21%
Professor 1 7%
Student > Bachelor 1 7%
Researcher 1 7%
Professor > Associate Professor 1 7%
Other 0 0%
Unknown 7 50%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 29%
Medicine and Dentistry 3 21%
Engineering 2 14%
Unknown 5 36%