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Colorectal Cancer

Overview of attention for book
Cover of 'Colorectal Cancer'

Table of Contents

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    Book Overview
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    Chapter 1 Cell Line Models of Molecular Subtypes of Colorectal Cancer
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    Chapter 2 Dissecting Oncogenic RTK Pathways in Colorectal Cancer Initiation and Progression
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    Chapter 3 Identification of Response Elements on Promoters Using Site-Directed Mutagenesis and Chromatin Immunoprecipitation
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    Chapter 4 Identification and Functional Analysis of Gene Regulatory Sequences Interacting with Colorectal Tumor Suppressors
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    Chapter 5 Methods for In Vivo Functional Studies of Chromatin-Modifying Enzymes in Early Steps of Colon Carcinogenesis
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    Chapter 6 The Colorectal Cancer Microenvironment: Strategies for Studying the Role of Cancer-Associated Fibroblasts
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    Chapter 7 Methods for Assessing Apoptosis and Anoikis in Normal Intestine/Colon and Colorectal Cancer
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    Chapter 8 Molecular Analysis of the Microbiome in Colorectal Cancer
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    Chapter 9 Proteomics Analysis of Colorectal Cancer Cells
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    Chapter 10 Autophagic Flux Assessment in Colorectal Cancer Cells
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    Chapter 11 Classification of Colorectal Cancer in Molecular Subtypes by Immunohistochemistry
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    Chapter 12 Stool DNA Integrity Method for Colorectal Cancer Detection
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    Chapter 13 RT-qPCR for Fecal Mature MicroRNA Quantification and Validation
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    Chapter 14 A Stool Multitarget mRNA Assay for the Detection of Colorectal Neoplasms
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    Chapter 15 Colorectal Cancer Detection Using Targeted LC-MS Metabolic Profiling
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    Chapter 16 Proteomic Profiling for Colorectal Cancer Biomarker Discovery
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    Chapter 17 Tumor-Derived Microparticles to Monitor Colorectal Cancer Evolution
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    Chapter 18 Molecular Testing for the Treatment of Advanced Colorectal Cancer: An Overview
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    Chapter 19 Testing Cell-Based Immunotherapy for Colorectal Cancer
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    Chapter 20 Patient-Derived Xenograft Models of Colorectal Cancer: Procedures for Engraftment and Propagation
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    Chapter 21 Use of Organoids to Characterize Signaling Pathways in Cancer Initiation
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    Chapter 22 Identification of Novel Molecules Targeting Cancer Stem Cells
Attention for Chapter 18: Molecular Testing for the Treatment of Advanced Colorectal Cancer: An Overview
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Chapter title
Molecular Testing for the Treatment of Advanced Colorectal Cancer: An Overview
Chapter number 18
Book title
Colorectal Cancer
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7765-9_18
Pubmed ID
Book ISBNs
978-1-4939-7764-2, 978-1-4939-7765-9
Authors

Patrick S. Lin, Thomas J. Semrad

Abstract

Concurrent with an expansion in the number of agents available for the treatment of advanced CRC, there has been an increase in our understanding of selection biomarkers to optimize the management of patients with this disease. For CRC patients being considered for anti-EGFR therapy, expanded RAS testing is the standard of care to determine the subset of patients who can benefit from cetuximab or panitumumab in conjunction with chemotherapy. A small fraction of patients have HER2 amplification where emerging data suggest treatment with drugs targeting this alteration. Although advanced CRC patients who harbor the BRAF V600E mutation have a poorer prognosis, they are eligible for combinatorial therapy targeting EGFR/BRAF or BRAF/MEK within the MAP kinase signaling pathway. Once primarily thought to be a negative prognostic marker, BRAF V600E mutation is now considered as a positive predictive factor with an opportunity for clinical intervention. A growing body of evidence also supports MSI testing as clinical benefits with immune checkpoint blockade by cancer immunotherapy have been demonstrated in MSI-high patients whose tumors exhibit high mutational burden. It has been established that UGT1A1*28 polymorphism is associated with irinotecan toxicity, but this test is rarely performed as the management strategy has not been identified. No established predictive biomarker for anti-VEGF therapy has yet to be discovered.It is becoming increasingly apparent that our growing understanding of biomarkers is revolutionizing and improving our strategies in the treatment of advanced CRC. Traditional nonselective cytotoxic chemotherapy is gradually being augmented and even in some cases supplanted by selective targeted agents based on our increasing understanding of tumor signaling and mechanism at the molecular level. The prospect of personalized medicine in directing treatment approaches that are optimally beneficial for patients brings tremendous excitement to the growing field of cancer therapeutics. As discussed in this chapter, the concurrent development of molecular biomarkers with new treatment strategies holds great promise of precision medicine in improving outcomes for patients with advanced CRC.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 25 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 25 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 16%
Researcher 4 16%
Student > Master 3 12%
Student > Postgraduate 2 8%
Professor 1 4%
Other 3 12%
Unknown 8 32%
Readers by discipline Count As %
Medicine and Dentistry 8 32%
Biochemistry, Genetics and Molecular Biology 2 8%
Mathematics 1 4%
Pharmacology, Toxicology and Pharmaceutical Science 1 4%
Agricultural and Biological Sciences 1 4%
Other 1 4%
Unknown 11 44%