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Targeting the DNA damage response fo...

Pollard, John.

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Targeting the DNA damage response for anti-cancer therapy

Record Type:	Electronic resources : Monograph/item
Title/Author:	Targeting the DNA damage response for anti-cancer therapy/ edited by John Pollard, Nicola Curtin.
other author:	Pollard, John.
Published:	Cham :Springer International Publishing : : 2018.,
Description:	ix, 401 p. :ill. (some col.), digital ;24 cm.
Contained By:	Springer eBooks
Subject:	Cancer - Treatment -
Online resource:	http://dx.doi.org/10.1007/978-3-319-75836-7
ISBN:	9783319758367

Targeting the DNA damage response for anti-cancer therapy
Targeting the DNA damage response for anti-cancer therapy[electronic resource] /edited by John Pollard, Nicola Curtin. - Cham :Springer International Publishing :2018. - ix, 401 p. :ill. (some col.), digital ;24 cm. - Cancer drug discovery and development,2196-9906. - Cancer drug discovery and development..

Over the past decade a complex role for DNA damage response (DDR) in tumorigenesis has emerged. A proficient DDR has been shown to be a primary cause for cellular resistance to the very many DNA damaging drugs, and IR, that are widely used as standard-of-care across multiple cancer types. It has also been shown that defects in this network, predominantly within the ATM mediated signaling pathway, are commonly observed in cancers and may be a primary event during tumorigenesis. Such defects may promote a genomically unstable environment, facilitating the persistence of mutations, any of which may provide a growth or survival advantage to the developing tumor. In addition, these somatic defects provide opportunities to exploit a reliance on remaining repair pathways for survival, a process which has been termed synthetic lethality. As a result of all these observations there has been a great interest in targeting the DDR to provide anti-cancer agents that may have benefit as monotherapy in cancers with high background DNA damage levels or as a means to increase the efficacy of DNA damaging drugs and IR. In this book we will review a series of important topics that are of great interest to a broad range of academic, industrial and clinical researchers, including the basic science of the DDR, its role in tumorigenesis and in dictating response to DNA damaging drugs and IR. Additionally, we will focus on the several proteins that have been targeted in attempts to provide drug candidates, each of which appear to have quite distinct profiles and could represent very different opportunities to provide patient benefit.

ISBN: 9783319758367

Standard No.: 10.1007/978-3-319-75836-7doiSubjects--Topical Terms:

1613890
Cancer
--Treatment

LC Class. No.: RC270.8 / .T374 2018

Dewey Class. No.: 616.99406

Targeting the DNA damage response for anti-cancer therapy
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245 0 0 $a Targeting the DNA damage response for anti-cancer therapy $h [electronic resource] / $c edited by John Pollard, Nicola Curtin.
260 $a Cham : $b Springer International Publishing : $b Imprint: Humana Press, $c 2018.
300 $a ix, 401 p. : $b ill. (some col.), digital ; $c 24 cm.
490 1 $a Cancer drug discovery and development, $x 2196-9906
520 $a Over the past decade a complex role for DNA damage response (DDR) in tumorigenesis has emerged. A proficient DDR has been shown to be a primary cause for cellular resistance to the very many DNA damaging drugs, and IR, that are widely used as standard-of-care across multiple cancer types. It has also been shown that defects in this network, predominantly within the ATM mediated signaling pathway, are commonly observed in cancers and may be a primary event during tumorigenesis. Such defects may promote a genomically unstable environment, facilitating the persistence of mutations, any of which may provide a growth or survival advantage to the developing tumor. In addition, these somatic defects provide opportunities to exploit a reliance on remaining repair pathways for survival, a process which has been termed synthetic lethality. As a result of all these observations there has been a great interest in targeting the DDR to provide anti-cancer agents that may have benefit as monotherapy in cancers with high background DNA damage levels or as a means to increase the efficacy of DNA damaging drugs and IR. In this book we will review a series of important topics that are of great interest to a broad range of academic, industrial and clinical researchers, including the basic science of the DDR, its role in tumorigenesis and in dictating response to DNA damaging drugs and IR. Additionally, we will focus on the several proteins that have been targeted in attempts to provide drug candidates, each of which appear to have quite distinct profiles and could represent very different opportunities to provide patient benefit.
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650 1 4 $a Biomedicine. $3 890831
650 2 4 $a Cancer Research. $3 891172
650 2 4 $a Gene Therapy. $3 600618
700 1 $a Pollard, John. $3 3332721
700 1 $a Curtin, Nicola. $3 3332722
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