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ErbB Receptor Signaling

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Cover of 'ErbB Receptor Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 ErbB Receptors and Cancer
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    Chapter 2 New Insights from Drosophila into the Regulation of EGFR Signaling
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    Chapter 3 C. elegans Vulva Induction: An In Vivo Model to Study Epidermal Growth Factor Receptor Signaling and Trafficking
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    Chapter 4 Targeting HER2 in Advanced Breast Cancer
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    Chapter 5 Methods to Investigate EGFR Ubiquitination
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    Chapter 6 Dimerization Assessment of Epithelial Growth Factor Family of Receptor Tyrosine Kinases by Using Cross-Linking Reagent
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    Chapter 7 Application of Immunofluorescence Staining to Study ErbB Family of Receptor Tyrosine Kinases
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    Chapter 8 Activation of Endosome-Associated Inert EGF Receptor Following Internalization
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    Chapter 9 Two-Pulse Endosomal Stimulation of Receptor Tyrosine Kinases Induces Cell Proliferation
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    Chapter 10 Study of EGFR Signaling/Endocytosis by Site-Directed Mutagenesis
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    Chapter 11 Using Percoll Gradient Fractionation to Study the Endocytic Trafficking of the EGFR
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    Chapter 12 Analysis of Epidermal Growth Factor Receptor-Induced Cell Motility by Wound Healing Assay
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    Chapter 13 Cell Cycle Synchronization of HeLa Cells to Assay EGFR Pathway Activation
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    Chapter 14 Analysis of Constitutive EGFR Signaling Regulating IRF3 Transcriptional Activity in Cancer Cells
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    Chapter 15 Measurement of Epidermal Growth Factor Receptor-Derived Signals Within Plasma Membrane Clathrin Structures
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    Chapter 16 Studying Nonproliferative Roles for Egfr Signaling in Tissue Morphogenesis Using Dorsal Closure of the Drosophila Embryo
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    Chapter 17 Analysis of Epithelial–Mesenchymal Transition Induced by Overexpression of Twist
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    Chapter 18 Assessment of Specificity of an Adenovirus Targeted to HER3/4
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    Chapter 19 Isolation of Human Mesenchymal Stem Cells for Studying ErbB Receptor Signaling
Attention for Chapter 14: Analysis of Constitutive EGFR Signaling Regulating IRF3 Transcriptional Activity in Cancer Cells
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Chapter title
Analysis of Constitutive EGFR Signaling Regulating IRF3 Transcriptional Activity in Cancer Cells
Chapter number 14
Book title
ErbB Receptor Signaling
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7219-7_14
Pubmed ID
Book ISBNs
978-1-4939-7218-0, 978-1-4939-7219-7
Authors

Gao Guo, Ke Gong, Amyn A. Habib

Abstract

Epidermal growth factor receptor (EGFR) plays an important role in various types of human cancers. Overexpression of EGFR leads to a constitutive tyrosine phosphorylation of multiple tyrosine residues in the EGFR. Recently, we have demonstrated that overexpressed EGFR oscillates between two distinct and mutually exclusive modes of signaling depending on the presence or absence of ligand. EGFR constitutively activates transcription factor IRF3, which results in transcription of its target genes. Addition of EGF causes a loss of IRF3 transcriptional activity and activation of canonical signaling pathways such as ERK. The mechanistic basis of this bimodal signaling appears to be the association of a distinct set of signaling proteins with EGFR in the absence or presence of ligand. In this chapter, we describe a detailed protocol for analyses of constitutive EGFR signaling with a focus on IRF3 target genes.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 100%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 2 100%