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Urothelial Carcinoma

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Cover of 'Urothelial Carcinoma'

Table of Contents

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    Book Overview
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    Chapter 1 Analysis of Chromosomal Alterations in Urothelial Carcinoma
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    Chapter 2 Analysis of Point Mutations in Clinical Samples of Urothelial Carcinoma
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    Chapter 3 A Versatile Assay for Detection of Aberrant DNA Methylation in Bladder Cancer.
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    Chapter 4 Immunohistochemical Analysis of Urothelial Carcinoma Tissues for Proliferation and Differentiation Markers
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    Chapter 5 Molecular Subtype Profiling of Urothelial Carcinoma Using a Subtype-Specific Immunohistochemistry Panel
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    Chapter 6 Defining the Pathways of Urogenital Schistosomiasis-Associated Urothelial Carcinogenesis through Transgenic and Bladder Wall Egg Injection Models.
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    Chapter 7 Algorithm for the Automated Evaluation of NAT2 Genotypes
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    Chapter 8 Detection of APOBEC3 Proteins and Catalytic Activity in Urothelial Carcinoma
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    Chapter 9 Oxidative Stress in Urothelial Carcinogenesis: Measurements of Protein Carbonylation and Intracellular Production of Reactive Oxygen Species
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    Chapter 10 Urothelial Carcinoma Stem Cells: Current Concepts, Controversies, and Methods.
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    Chapter 11 In Vitro Differentiation and Propagation of Urothelium from Pluripotent Stem Cell Lines.
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    Chapter 12 Spheroid Cultures of Primary Urothelial Cancer Cells: Cancer Tissue-Originated Spheroid (CTOS) Method
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    Chapter 13 The N-butyl-N-4-hydroxybutyl Nitrosamine Mouse Urinary Bladder Cancer Model.
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    Chapter 14 Patient-Derived Bladder Cancer Xenografts
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    Chapter 15 Orthotopic Mouse Models of Urothelial Cancer
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    Chapter 16 Quantification of MicroRNAs in Urine-Derived Specimens.
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    Chapter 17 Quantitative RNA Analysis from Urine Using Real Time PCR
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    Chapter 18 DNA Methylation Analysis from Body Fluids.
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    Chapter 19 Urinary Protein Markers for the Detection and Prognostication of Urothelial Carcinoma
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    Chapter 20 Isolation and Characterization of CTCs from Patients with Cancer of a Urothelial Origin
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    Chapter 21 Epigenetic Treatment Options in Urothelial Carcinoma.
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    Chapter 22 Evaluation of Protein Levels of the Receptor Tyrosine Kinase ErbB3 in Serum
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    Chapter 23 Targeting the PI3K/AKT/mTOR Pathway in Bladder Cancer
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    Chapter 24 Visualization and Quantitative Measurement of Drug-Induced Platinum Adducts in the Nuclear DNA of Individual Cells by an Immuno-Cytological Assay
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    Chapter 25 Erratum to: Urinary Protein Markers for the Detection and Prognostication of Urothelial Carcinoma
Attention for Chapter 22: Evaluation of Protein Levels of the Receptor Tyrosine Kinase ErbB3 in Serum
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Chapter title
Evaluation of Protein Levels of the Receptor Tyrosine Kinase ErbB3 in Serum
Chapter number 22
Book title
Urothelial Carcinoma
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7234-0_22
Pubmed ID
Book ISBNs
978-1-4939-7233-3, 978-1-4939-7234-0
Authors

Leandro S. D’Abronzo, Chong-Xian Pan, Paramita M. Ghosh, D’Abronzo, Leandro S., Pan, Chong-Xian, Ghosh, Paramita M.

Abstract

The epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases (RTK) consists of four members: EGFR1/ErbB1/HER1, ErbB2/HER2, ErbB3/HER3, and HER4/ErbB4. Signaling through these receptors regulates many key cellular activities, such as cell division, migration, adhesion, differentiation, and apoptosis. The ErbB family has been shown to be overexpressed in different types of cancers and is a target of several inhibitors already in clinical trials. ErbB3 lacks a functional tyrosine kinase domain and therefore has not been as extensively studied as the other members of this family, but its importance in activating downstream pathways, such as the PI3K/Akt pathway, makes this RTK a worthy investigation target, especially in urothelial carcinoma where the PI3K/Akt pathway is vital for progression. In recent times, ErbB3 overexpression has been linked to drug resistance and progression of various diseases, especially cancer. ErbB3 levels in the serum were shown in many cases to be reflective of its role in disease progression, and therefore detection of serum ErbB3 levels during treatment may be of importance.Here we describe two methods for detecting ErbB3 protein in serum from patients who have undergone a clinical trial, utilizing two well-established methods in molecular biology-western blotting and ELISA, focusing on sample preparation and troubleshooting.

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Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 22%
Other 2 22%
Student > Bachelor 1 11%
Student > Master 1 11%
Unknown 3 33%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 2 22%
Biochemistry, Genetics and Molecular Biology 2 22%
Sports and Recreations 1 11%
Medicine and Dentistry 1 11%
Unknown 3 33%