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Status: Bibliographieeintrag

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Verfasst von:Herrmann, Jonas [VerfasserIn]   i
 Schmidt, Helena [VerfasserIn]   i
 Nitschke, Katja [VerfasserIn]   i
 Weis, Cleo-Aron Thias [VerfasserIn]   i
 Nuhn, Philipp [VerfasserIn]   i
 Hardenberg, Jost von [VerfasserIn]   i
 Michel, Maurice Stephan [VerfasserIn]   i
 Erben, Philipp [VerfasserIn]   i
 Worst, Thomas [VerfasserIn]   i
Titel:RNA expression of DNA damage response genes in muscle-invasive bladder cancer
Titelzusatz:influence on outcome and response to adjuvant cisplatin-based chemotherapy
Verf.angabe:Jonas Herrmann, Helena Schmidt, Katja Nitschke, Cleo-Aron Weis, Philipp Nuhn, Jost von Hardenberg, Maurice Stephan Michel, Philipp Erben, Thomas Stefan Worst
E-Jahr:2021
Jahr:18 April 2021
Umfang:12 S.
Fussnoten:Gesehen am 26.07.2021
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2021
Band/Heft Quelle:22(2021), 8, Artikel-ID 4188, Seite 1-12
ISSN Quelle:1422-0067
 1661-6596
Abstract:Background: Perioperative cisplatin-based chemotherapy (CBC) can improve the outcome of patients with muscle-invasive bladder cancer (MIBC), but it is still to be defined which patients benefit. Mutations in DNA damage response genes (DDRG) can predict the response to CBC. The value of DDRG expression as a marker of CBC treatment effect remains unclear. Material and methods: RNA expression of the nine key DDRG (BCL2, BRCA1, BRCA2, ERCC2, ERCC6, FOXM1, RAD50, RAD51, and RAD52) was assessed by qRT-PCR in a cohort of 61 MICB patients (median age 66 y, 48 males, 13 females) who underwent radical cystectomy in a tertiary care center. The results were validated in the The Cancer Genome Atlas (TCGA) cohort of MIBC (n = 383). Gene expression was correlated with disease-free survival (DFS) and overall survival (OS). Subgroup analyses were performed in patients who received adjuvant cisplatin-based chemotherapy (ACBC) (Mannheim n = 20 and TCGA n = 75). Results: Low expression of RAD52 was associated with low DFS in both the Mannheim and the TCGA cohorts (Mannheim: p = 0.039; TCGA: p = 0.017). This was especially apparent in subgroups treated with ACBC (Mannheim: p = 0.0059; TCGA: p = 0.012). Several other genes showed an influence on DFS in the Mannheim cohort (BRCA2, ERCC2, FOXM1) where low expression was associated with poor DFS (p < 0.05 for all). This finding was not fully supported by the data in the TCGA cohort, where high expression of FOXM1 and BRCA2 correlated with poor DFS. Conclusion: Low expression of RAD52 correlated with decreased DFS in the Mannheim and the TCGA cohort. This effect was especially pronounced in the subset of patients who received ACBC, making it a promising indicator for response to ACBC on the level of gene expression.
DOI:doi:10.3390/ijms22084188
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: https://doi.org/10.3390/ijms22084188
 Volltext: https://www.mdpi.com/1422-0067/22/8/4188
 DOI: https://doi.org/10.3390/ijms22084188
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:<i>BCL2</i>
 <i>BRCA1</i>
 <i>BRCA2</i>
 <i>ERCC2</i>
 <i>ERCC6</i>
 <i>FOXM1</i>
 <i>RAD50</i>
 <i>RAD51</i>
 <i>RAD52</i>
 adjuvant chemotherapy
 cisplatin
 DNA-damage response
 muscle-invasive bladder cancer
K10plus-PPN:1764593227
Verknüpfungen:→ Zeitschrift

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