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Kinesins and Cancer

Editat de Frank Kozielski, FSB
en Limba Engleză Hardback – 24 mar 2015
This interdisciplinary volume collates research work on kinesins and cancer. Authors attempt to validate members of the kinesin superfamily as potential targets for drug development in cancer chemotherapy. The work begins by highlighting the importance of kinesins, summarising current knowledge and how they are shown to be crucial for mitosis. Chapters go on to explore how this family of proteins are emerging as a novel target for chemotherapeutic intervention and drug development.
Readers will learn how kinesins travel along microtubules to fulfill their many roles in intracellular transport or cell division. Several compounds that inhibit two mitotic kinesins (called Eg5 and CENP-E) have entered Phase I and II clinical trials and are explored in these chapters. Additional mitotic kinesins are currently being validated as drug targets, raising the possibility that the repertoire of kinesin-based drug targets may expand in the future.
The book is suitable as a reference standard for the field of kinesins and cancer. It will interest those in academia and pharmaceutical companies, and anyone with an interest in the medical relevance of these proteins, which cutting edge methodologies are now enabling us to understand in astonishing detail.
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Specificații

ISBN-13: 9789401797313
ISBN-10: 9401797315
Pagini: 271
Ilustrații: X, 271 p. 50 illus., 32 illus. in color.
Dimensiuni: 155 x 235 x 18 mm
Greutate: 0.58 kg
Ediția:2015
Editura: SPRINGER NETHERLANDS
Colecția Springer
Locul publicării:Dordrecht, Netherlands

Public țintă

Research

Cuprins

Preface.- The kinesin superfamily.- The discovery and development of Eg5 inhibitors for the clinic.- Mechanism of action of Eg5 inhibitors.- Clinical trials of mitotic kinesin inhibitors.- Kif15; a useful target for anti-cancer therapy?.- Down-regulating CENP-E activity: for better or for worse.- The human kinesin-14 motor KifC1/HSET is an attractive anti-cancer drug target.-Kinesin-13 Microtubule Depolymerizing Proteins as targets for cancer therapy.- Chromokinesins in genome maintenance and cancer.- Kif14: a clinically relevant kinesin and potential target for cancer therapy.- Kinesin-8 members and their potential as biomarker or therapeutic target.- The kinesin-6 members MKLP1, MKLP2 and MPP.- Non-motor spindle proteins as cancer chemotherapy targets.- Inhibitors of mitotic kinesins for cancer treatment: consequences for neurons.- Index.

Textul de pe ultima copertă

This interdisciplinary volume collates research work on kinesins and cancer. Authors attempt to validate members of the kinesin superfamily as potential targets for drug development in cancer chemotherapy. The work begins by highlighting the importance of kinesins, summarising current knowledge and how they are shown to be crucial for mitosis. Chapters go on to explore how this family of proteins are emerging as a novel target for chemotherapeutic intervention and drug development.
Readers will learn how kinesins travel along microtubules to fulfill their many roles in intracellular transport or cell division. Several compounds that inhibit two mitotic kinesins (called Eg5 and CENP-E) have entered Phase I and II clinical trials and are explored in these chapters. Additional mitotic kinesins are currently being validated as drug targets, raising the possibility that the repertoire of kinesin-based drug targets may expand in the future.
The book is suitable as a reference standard for the field of kinesins and cancer. It will interest those in academia and pharmaceutical companies, and anyone with an interest in the medical relevance of these proteins, which cutting edge methodologies are now enabling us to understand in astonishing detail.

Caracteristici

Covers the entire, interdisciplinary field of kinesins and cancer through expert contributions Offers a timely reference standard on the relevance of kinesins to cancer treatment Contributes to potential initial validation of mitotic kinesins as targets for drug development in cancer chemotherapy