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Cyclin-Dependent Kinase (CDK) Inhibitors

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Cover of 'Cyclin-Dependent Kinase (CDK) Inhibitors'

Table of Contents

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    Book Overview
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    Chapter 1 Cyclin-Dependent Kinase (CDK) Inhibitors
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    Chapter 2 Expression and Purification of Recombinant Cyclins and CDKs for Activity Evaluation
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    Chapter 3 Expression and Purification of Recombinant CDKs: CDK7, CDK8, and CDK9
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    Chapter 4 Preparation of CDK/Cyclin Inhibitor Complexes for Structural Determination
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    Chapter 5 Fragment-Based De Novo Design of Cyclin-Dependent Kinase 2 Inhibitors
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    Chapter 6 Protein-Protein Interaction for the De Novo Design of Cyclin-Dependent Kinase Peptide Inhibitors
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    Chapter 7 Identification of Cyclin A Binders with a Fluorescent Peptide Sensor
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    Chapter 8 Cyclin-Dependent Kinase (CDK) Inhibitors
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    Chapter 9 Analysis of CDK Inhibitor Action on Mitochondria-Mediated Apoptosis
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    Chapter 10 Evaluating the Effects of CDK Inhibitors in Ischemia–Reperfusion Injury Models
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    Chapter 11 Assessing Cell Cycle Independent Function of the CDK Inhibitor p21(CDKN1A) in DNA Repair.
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    Chapter 12 Drug Delivery Strategies of Chemical CDK Inhibitors
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    Chapter 13 Animal Models for Studying the In Vivo Functions of Cell Cycle CDKs.
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    Chapter 14 Evaluating Chemical CDK Inhibitors as Cell Death Inducers
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    Chapter 15 Models for the Study of the Cross Talk Between Inflammation and Cell Cycle
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    Chapter 16 Metabolomic Applications to the Characterization of the Mode-of-Action of CDK Inhibitors
Attention for Chapter 14: Evaluating Chemical CDK Inhibitors as Cell Death Inducers
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Chapter title
Evaluating Chemical CDK Inhibitors as Cell Death Inducers
Chapter number 14
Book title
Cyclin-Dependent Kinase (CDK) Inhibitors
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-2926-9_14
Pubmed ID
Book ISBNs
978-1-4939-2925-2, 978-1-4939-2926-9
Authors

Hiroshi Hirai, Yoko Nakatsuru

Abstract

The cell cycle of eukaryotic cells is regulated by a family of protein kinases called cyclin-dependent kinases (Cdks). We have reported the identification and biological characterization of a highly potent, small-molecule pan-Cdk inhibitor, which inhibited Cdk1, 2, 4, 5, 6, and 9 with equal potency in the nM range. This compound inhibited multiple events in the cell cycle and induced cell death in human cancer cell lines as well as in peripheral blood or purified resting lymphocytes ex vivo. We describe the materials and methods to determine antitumor efficacy in vivo xenograft models. Pharmacodynamic marker assays that have been performed using tumors and normal tissues are explained. Moreover, we briefly describe methods for determining the effects of chemical Cdk inhibitors on peripheral blood cells or lymphocytes ex vivo.