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Bacterial Therapy of Cancer

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Cover of 'Bacterial Therapy of Cancer'

Table of Contents

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    Book Overview
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    Chapter 1 Tumor-Targeting Salmonella typhimurium A1-R: An Overview.
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    Chapter 2 Enhancement of Tumor-Targeted Delivery of Bacteria with Nitroglycerin Involving Augmentation of the EPR Effect
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    Chapter 3 Oral Delivery of Tumor-Targeting Salmonella to Treat Cancer in Mice
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    Chapter 4 Microfluidic Device to Quantify the Behavior of Therapeutic Bacteria in Three-Dimensional Tumor Tissue.
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    Chapter 5 Tumor-Targeting Therapy Using Gene-Engineered Anaerobic-Nonpathogenic Bifidobacterium longum.
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    Chapter 6 Noninvasive In Vivo Imaging to Follow Bacteria Engaged in Cancer Therapy
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    Chapter 7 In Vivo Bioluminescence Imaging of Intratumoral Bacteria
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    Chapter 8 Employment of Salmonella in Cancer Gene Therapy
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    Chapter 9 Development of a Targeted Gene-Delivery System Using Escherichia coli
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    Chapter 10 Isolation and Analysis of Suppressor Mutations in Tumor-Targeted msbB Salmonella
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    Chapter 11 Determination of Plasmid Segregational Stability in a Growing Bacterial Population
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    Chapter 12 Visualization of Anticancer Salmonella typhimurium Engineered for Remote Control of Therapeutic Proteins
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    Chapter 13 Methods for Tumor Targeting with Salmonella typhimurium A1-R.
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    Chapter 14 Salmonella typhimurium A1-R and Cell-Cycle Decoy Therapy of Cancer.
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    Chapter 15 Future of Bacterial Therapy of Cancer
Attention for Chapter 11: Determination of Plasmid Segregational Stability in a Growing Bacterial Population
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Chapter title
Determination of Plasmid Segregational Stability in a Growing Bacterial Population
Chapter number 11
Book title
Bacterial Therapy of Cancer
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3515-4_11
Pubmed ID
Book ISBNs
978-1-4939-3513-0, 978-1-4939-3515-4
Authors

M. Gabriela Kramer

Abstract

Bacterial plasmids are extensively used as cloning vectors for a number of genes for academic and commercial purposes. Moreover, attenuated bacteria carrying recombinant plasmids expressing genes with anti-tumor activity have shown promising therapeutic results in animal models of cancer. Equitable plasmid distribution between daughter cells during cell division, i.e., plasmid segregational stability, depends on many factors, including the plasmid copy number, its replication mechanism, the levels of recombinant gene expression, the type of bacterial host, and the metabolic burden associated with all these factors. Plasmid vectors usually code for antibiotic-resistant functions, and, in order to enrich the culture with bacteria containing plasmids, antibiotic selective pressure is commonly used to eliminate plasmid-free segregants from the growing population. However, administration of antibiotics can be inconvenient for many industrial and therapeutic applications. Extensive ongoing research is being carried out to develop stably-inherited plasmid vectors. Here, I present an easy and precise method for determining the kinetics of plasmid loss or maintenance for every ten generations of bacterial growth in culture.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Uruguay 1 10%
Unknown 9 90%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 20%
Student > Ph. D. Student 2 20%
Unspecified 1 10%
Student > Master 1 10%
Researcher 1 10%
Other 1 10%
Unknown 2 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 50%
Unspecified 1 10%
Engineering 1 10%
Unknown 3 30%