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Oncogene-Induced Senescence

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Cover of 'Oncogene-Induced Senescence'

Table of Contents

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    Book Overview
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    Chapter 1 The Immortal Senescence
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    Chapter 2 Senescence Phenotypes Induced by Ras in Primary Cells
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    Chapter 3 Cellular Model of p21-Induced Senescence
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    Chapter 4 Detecting Markers of Therapy-Induced Senescence in Cancer Cells
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    Chapter 5 Genome-Wide miRNA Screening for Genes Bypassing Oncogene-Induced Senescence
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    Chapter 6 Detection of Dysfunctional Telomeres in Oncogene-Induced Senescence
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    Chapter 7 RT-qPCR Detection of Senescence-Associated Circular RNAs
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    Chapter 8 Oncogene-Induced Senescence
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    Chapter 9 Detecting the Senescence-Associated Secretory Phenotype (SASP) by High Content Microscopy Analysis
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    Chapter 10 Sudan Black B, The Specific Histochemical Stain for Lipofuscin: A Novel Method to Detect Senescent Cells
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    Chapter 11 Using [U- 13 C 6 ]-Glucose Tracer to Study Metabolic Changes in Oncogene-Induced Senescence Fibroblasts
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    Chapter 12 Detection of the Ubiquitinome in Cells Undergoing Oncogene-Induced Senescence
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    Chapter 13 Detection of Reactive Oxygen Species in Cells Undergoing Oncogene-Induced Senescence
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    Chapter 14 Detection of Senescent Cells by Extracellular Markers Using a Flow Cytometry-Based Approach
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    Chapter 15 Metabolic Changes Investigated by Proton NMR Spectroscopy in Cells Undergoing Oncogene-Induced Senescence
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    Chapter 16 Oncogene-Induced Senescence
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    Chapter 17 Senescence-Like Phenotypes in Human Nevi
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    Chapter 18 Detection of Oncogene-Induced Senescence In Vivo
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    Chapter 19 Detection of Senescence Markers During Mammalian Embryonic Development
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    Chapter 20 Induction and Detection of Oncogene-Induced Cellular Senescence in Drosophila
Attention for Chapter 11: Using [U- 13 C 6 ]-Glucose Tracer to Study Metabolic Changes in Oncogene-Induced Senescence Fibroblasts
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Chapter title
Using [U- 13 C 6 ]-Glucose Tracer to Study Metabolic Changes in Oncogene-Induced Senescence Fibroblasts
Chapter number 11
Book title
Oncogene-Induced Senescence
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6670-7_11
Pubmed ID
Book ISBNs
978-1-4939-6668-4, 978-1-4939-6670-7
Authors

Katerina I. Leonova, David A. Scott, Leonova, Katerina I., Scott, David A.

Abstract

Metabolic flux analysis (MFA) is a comprehensive technique that allows researchers to create a map of cellular metabolic state. This method is extensively studied in the literature in the context of the metabolism of various cancer cells, and it normally utilizes a labeled substrate that is absorbed by the cells, the levels of the incorporation are measured by mass spectrometry (MS) within the pool of metabolites and computational estimation is performed. Here, we propose the use of this assay to study metabolic changes that occur in oncogene-induced senescence (OIS) of normal human fibroblasts (Wi38) versus those in the state of proliferation/quiescence.

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Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 63%
Researcher 1 13%
Student > Master 1 13%
Unknown 1 13%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 38%
Agricultural and Biological Sciences 1 13%
Earth and Planetary Sciences 1 13%
Medicine and Dentistry 1 13%
Engineering 1 13%
Other 0 0%
Unknown 1 13%