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Oncogene-Induced Senescence

Overview of attention for book
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
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Chapter title
Oncogene-Induced Senescence
Chapter number 16
Book title
Oncogene-Induced Senescence
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6670-7_16
Pubmed ID
Book ISBNs
978-1-4939-6668-4, 978-1-4939-6670-7
Authors

Nikiforov, Mikhail A, Shewach, Donna S, Mikhail A. Nikiforov, Donna S. Shewach, Nikiforov, Mikhail A., Shewach, Donna S.

Abstract

DNA damage response has been characterized as an important mediator of senescence phenotypes induced by activated oncogenes in normal human cells. Depletion of intracellular deoxyribonucleotide pools has been recently recognized as one of the major causes for DNA damage in these cells. Cells undergoing oncogene-induced senescence display decreased expression of several rate-limiting enzymes involved in the biosynthesis of deoxyribonucleotides, including thymidylate synthase (TS) and ribonucleotide reductase (RR). Individual depletion of these enzymes leads to premature senescence. Reciprocally, ectopic expression of TS and RR or addition of deoxyribonucleosides resulted in suppression of senescence phenotypes in normal or tumor cells caused by overexpression of activated HRAS or depletion of C-MYC, respectively. Therefore, in the current chapter, we will describe a methodology for the quantitative measurement of nucleotide pools in senescent cells.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 40%
Student > Bachelor 1 20%
Student > Ph. D. Student 1 20%
Unknown 1 20%
Readers by discipline Count As %
Medicine and Dentistry 2 40%
Agricultural and Biological Sciences 1 20%
Unknown 2 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 06 November 2016.
All research outputs
#20,351,881
of 22,899,952 outputs
Outputs from Methods in molecular biology
#9,922
of 13,134 outputs
Outputs of similar age
#355,310
of 420,444 outputs
Outputs of similar age from Methods in molecular biology
#845
of 1,074 outputs
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