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Tumor Immune Microenvironment in Cancer Progression and Cancer Therapy

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Cover of 'Tumor Immune Microenvironment in Cancer Progression and Cancer Therapy'

Table of Contents

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    Book Overview
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    Chapter 1 Tumor Immuno-Environment in Cancer Progression and Therapy
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    Chapter 2 Cancer Immunotherapy Targets Based on Understanding the T Cell-Inflamed Versus Non-T Cell-Inflamed Tumor Microenvironment
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    Chapter 3 Regulation of CTL Infiltration Within the Tumor Microenvironment
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    Chapter 4 The Role of Tumor Microenvironment in Cancer Immunotherapy
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    Chapter 5 Immunogenic and Non-immunogenic Cell Death in the Tumor Microenvironment
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    Chapter 6 Exosomes in Cancer: Another Mechanism of Tumor-Induced Immune Suppression
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    Chapter 7 Chemo-Immunotherapy: Role of Indoleamine 2,3-Dioxygenase in Defining Immunogenic Versus Tolerogenic Cell Death in the Tumor Microenvironment
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    Chapter 8 Targeting Myeloid-Derived Suppressor Cells in Cancer
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    Chapter 9 Tryptophan Catabolism and Cancer Immunotherapy Targeting IDO Mediated Immune Suppression
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    Chapter 10 Lipid Inflammatory Mediators in Cancer Progression and Therapy
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    Chapter 11 Oncolytic Virotherapy and the Tumor Microenvironment
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    Chapter 12 The Impact of Housing Temperature-Induced Chronic Stress on Preclinical Mouse Tumor Models and Therapeutic Responses: An Important Role for the Nervous System
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    Chapter 13 Immunotherapeutic Targeting of Tumor-Associated Blood Vessels
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    Chapter 14 Adaptive Resistance to Cancer Immunotherapy
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    Chapter 15 Imaging the Tumor Microenvironment
Attention for Chapter 11: Oncolytic Virotherapy and the Tumor Microenvironment
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Chapter title
Oncolytic Virotherapy and the Tumor Microenvironment
Chapter number 11
Book title
Tumor Immune Microenvironment in Cancer Progression and Cancer Therapy
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-3-319-67577-0_11
Pubmed ID
Book ISBNs
978-3-31-967575-6, 978-3-31-967577-0
Authors

Sara E. Berkey, Steve H. Thorne, David L. Bartlett

Abstract

Oncolytic viral therapy is a promising approach to treat many malignancies, including breast, colorectal, hepatocellular, and melanoma. The best results are seen when using "targeted and armed" viruses. These are viruses that have been genetically modified to selectively replicate within cancer cells and express specific transgenes that alter the tumor microenvironment to inhibit tumor progression. The products of these transgenes induce cell death, make the virus less virulent, compromise tumor vascularity, and are capable of modulating or enhancing the immune system-such as cytokines and chemokines. In addition, oncolytic viruses can induce anti-vascular effects and disrupt the extracellular matrix to improve viral spread within the tumor. Oncolytic viruses also improve crosstalk between fibroblasts, cytokine-induced killer cells, and cancer cells within the microenvironment, leading to enhanced tumor cell death.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 34 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 24%
Student > Bachelor 4 12%
Researcher 3 9%
Student > Master 3 9%
Professor 1 3%
Other 1 3%
Unknown 14 41%
Readers by discipline Count As %
Agricultural and Biological Sciences 8 24%
Biochemistry, Genetics and Molecular Biology 7 21%
Medicine and Dentistry 3 9%
Immunology and Microbiology 1 3%
Unknown 15 44%