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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 1: The Immortal Senescence
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Chapter title
The Immortal Senescence
Chapter number 1
Book title
Oncogene-Induced Senescence
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6670-7_1
Pubmed ID
Book ISBNs
978-1-4939-6668-4, 978-1-4939-6670-7
Authors

Anna Bianchi-Smiraglia, Brittany C. Lipchick, Mikhail A. Nikiforov, Bianchi-Smiraglia, Anna, Lipchick, Brittany C., Nikiforov, Mikhail A.

Abstract

Activation of oncogenic signaling paradoxically results in the permanent withdrawal from cell cycle and induction of senescence (oncogene-induced senescence (OIS)). OIS is a fail-safe mechanism used by the cells to prevent uncontrolled tumor growth, and, as such, it is considered as the first barrier against cancer. In order to progress, tumor cells thus need to first overcome the senescent phenotype. Despite the increasing attention gained by OIS in the past 20 years, this field is still rather young due to continuous emergence of novel pathways and processes involved in OIS. Among the many factors contributing to incomplete understanding of OIS are the lack of unequivocal markers for senescence and the complexity of the phenotypes revealed by senescent cells in vivo and in vitro. OIS has been shown to play major roles at both the cellular and organismal levels in biological processes ranging from embryonic development to barrier to cancer progression. Here we will briefly outline major advances in methodologies that are being utilized for induction, identification, and characterization of molecular processes in cells undergoing oncogene-induced senescence. The full description of such methodologies is provided in the corresponding chapters of the book.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 5 26%
Researcher 3 16%
Student > Ph. D. Student 2 11%
Student > Bachelor 1 5%
Other 1 5%
Other 1 5%
Unknown 6 32%
Readers by discipline Count As %
Agricultural and Biological Sciences 7 37%
Biochemistry, Genetics and Molecular Biology 3 16%
Medicine and Dentistry 2 11%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Unknown 6 32%