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Status: Bibliographieeintrag

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Verfasst von:Liu, Chun-Shan [VerfasserIn]   i
 Toth, Reka [VerfasserIn]   i
 Bakr, Ali [VerfasserIn]   i
 Goyal, Ashish [VerfasserIn]   i
 Islam, Md Saiful [VerfasserIn]   i
 Breuer, Kersten [VerfasserIn]   i
 Mayakonda Thippeswamy, Anand [VerfasserIn]   i
 Lin, Yu-Yu [VerfasserIn]   i
 Stepper, Peter [VerfasserIn]   i
 Jurkowski, Tomasz P. [VerfasserIn]   i
 Veldwijk, Marlon Romano [VerfasserIn]   i
 Sperk, Elena [VerfasserIn]   i
 Herskind, Carsten [VerfasserIn]   i
 Lutsik, Pavlo [VerfasserIn]   i
 Weichenhan, Dieter [VerfasserIn]   i
 Plass, Christoph [VerfasserIn]   i
 Schmezer, Peter [VerfasserIn]   i
 Popanda, Odilia [VerfasserIn]   i
Titel:Epigenetic modulation of radiation-induced diacylglycerol kinase alpha expression prevents pro-fibrotic fibroblast response
Verf.angabe:Chun-Shan Liu, Reka Toth, Ali Bakr, Ashish Goyal, Md Saiful Islam, Kersten Breuer, Anand Mayakonda, Yu-Yu Lin, Peter Stepper, Tomasz P. Jurkowski, Marlon R. Veldwijk, Elena Sperk, Carsten Herskind, Pavlo Lutsik, Dieter Weichenhan, Christoph Plass, Peter Schmezer and Odilia Popanda
E-Jahr:2021
Jahr:18 May 2021
Umfang:26 S.
Fussnoten:Gesehen am 29.09.2021
Titel Quelle:Enthalten in: Cancers
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2021
Band/Heft Quelle:13(2021), 10 vom: Mai, Artikel-ID 2455, Seite 1-26
ISSN Quelle:2072-6694
Abstract:Radiotherapy, a common component in cancer treatment, can induce adverse effects including fibrosis in co-irradiated tissues. We previously showed that differential DNA methylation at an enhancer of diacylglycerol kinase alpha (DGKA) in normal dermal fibroblasts is associated with radiation-induced fibrosis. After irradiation, the transcription factor EGR1 is induced and binds to the hypomethylated enhancer, leading to increased DGKA and pro-fibrotic marker expression. We now modulated this DGKA induction by targeted epigenomic and genomic editing of the DGKA enhancer and administering epigenetic drugs. Targeted DNA demethylation of the DGKA enhancer in HEK293T cells resulted in enrichment of enhancer-related histone activation marks and radiation-induced DGKA expression. Mutations of the EGR1-binding motifs decreased radiation-induced DGKA expression in BJ fibroblasts and caused dysregulation of multiple fibrosis-related pathways. EZH2 inhibitors (GSK126, EPZ6438) did not change radiation-induced DGKA increase. Bromodomain inhibitors (CBP30, JQ1) suppressed radiation-induced DGKA and pro-fibrotic marker expression. Similar drug effects were observed in donor-derived fibroblasts with low DNA methylation. Overall, epigenomic manipulation of DGKA expression may offer novel options for a personalized treatment to prevent or attenuate radiotherapy-induced fibrosis.
DOI:doi:10.3390/cancers13102455
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/cancers13102455
 Volltext: https://www.mdpi.com/2072-6694/13/10/2455
 DOI: https://doi.org/10.3390/cancers13102455
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:bromodomain inhibitors
 DNA methylation
 EZH2 inhibitors
 radiotherapy-induced fibrosis
K10plus-PPN:1772032441
Verknüpfungen:→ Zeitschrift

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