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Status: Bibliographieeintrag

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Verfasst von:Tapia-Laliena, María Angeles [VerfasserIn]   i
 Korzeniewski, Nina [VerfasserIn]   i
 Hohenfellner, Markus [VerfasserIn]   i
 Duensing, Stefan [VerfasserIn]   i
Titel:High-risk prostate cancer
Titelzusatz:a disease of genomic instability
Verf.angabe:María A. Tapia-Laliena, Nina Korzeniewski, Markus Hohenfellner, Stefan Duensing
E-Jahr:2014
Jahr:13 June 2014
Umfang:7 S.
Fussnoten:Gesehen am 25.08.2020
Titel Quelle:Enthalten in: Urologic oncology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1995
Jahr Quelle:2014
Band/Heft Quelle:32(2014), 8, Seite 1101-1107
ISSN Quelle:1873-2496
Abstract:Objectives - In this review, we will discuss the latest advances in our understanding of the relationship between the cellular DNA damage response and genomic instability in prostate cancer and the emerging possibilities to exploit these aberrations as prognostic biomarkers and guides for personalized patient management. - Methods - Important findings related to genomic instability in prostate cancer were retrieved from the literature and combined with our own results and a translational perspective. - Results - Prostate cancer is characterized by a highly altered genomic landscape with a wide spectrum of genomic alterations, including somatic mutations, copy number alterations (CNAs), gene fusions, complex chromosomal rearrangements, and aneuploidy. In addition, massive DNA damaging events, including chromothripsis and chromoplexy, which can lead to extensive genomic insults in a single step, have been identified. A number of these genomic aberrations have been found to provide prognostic information and can therefore help to identify high-risk patients. In addition, defects in the DNA damage checkpoint and repair machinery can potentially be harnessed for therapeutic purposes. - Conclusions - Genomic instability plays a crucial role in the malignant progression of prostate cancer and can be exploited for the development of novel prognostic biomarkers and innovative therapies.
DOI:doi:10.1016/j.urolonc.2014.02.005
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.urolonc.2014.02.005
 Volltext: http://www.sciencedirect.com/science/article/pii/S1078143914000362
 DOI: https://doi.org/10.1016/j.urolonc.2014.02.005
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Biomarkers
 DNA damage
 Genomic instability
 Prostate cancer
 Somatic mutations
 Translational therapeutics
K10plus-PPN:1727751922
Verknüpfungen:→ Zeitschrift

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