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Status: Bibliographieeintrag

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Verfasst von:Rassamegevanon, Treewut [VerfasserIn]   i
 Feindt, Louis [VerfasserIn]   i
 Koi, Lydia [VerfasserIn]   i
 Müller, Johannes [VerfasserIn]   i
 Freudenberg, Robert [VerfasserIn]   i
 Löck, Steffen [VerfasserIn]   i
 Sihver, Wiebke [VerfasserIn]   i
 Çevik, Enes [VerfasserIn]   i
 Kühn, Ariane Christel [VerfasserIn]   i
 von Neubeck, Cläre [VerfasserIn]   i
 Linge, Annett [VerfasserIn]   i
 Pietzsch, Hans-Jürgen [VerfasserIn]   i
 Kotzerke, Jörg [VerfasserIn]   i
 Baumann, Michael [VerfasserIn]   i
 Krause, Mechthild [VerfasserIn]   i
 Dietrich, Antje [VerfasserIn]   i
Titel:Molecular response to combined molecular- and external radiotherapy in head and neck squamous cell carcinoma (HNSCC)
Verf.angabe:Treewut Rassamegevanon, Louis Feindt, Lydia Koi, Johannes Müller, Robert Freudenberg, Steffen Löck, Wiebke Sihver, Enes Çevik, Ariane Christel Kühn, Cläre von Neubeck, Annett Linge, Hans-Jürgen Pietzsch, Jörg Kotzerke, Michael Baumann, Mechthild Krause and Antje Dietrich
E-Jahr:2021
Jahr:9 November 2021
Umfang:16 S.
Fussnoten:Gesehen am 26.01.2022 ; This article belongs to the special issue "Cancer radiotherapy"
Titel Quelle:Enthalten in: Cancers
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2021
Band/Heft Quelle:13(2021), 22, special issue, Artikel-ID 5595, Seite 1-16
ISSN Quelle:2072-6694
Abstract:Combination treatment of molecular targeted and external radiotherapy is a promising strategy and was shown to improve local tumor control in a HNSCC xenograft model. To enhance the therapeutic value of this approach, this study investigated the underlying molecular response. Subcutaneous HNSCC FaDuDD xenografts were treated with single or combination therapy (X-ray: 0, 2, 4 Gy; anti-EGFR antibody (Cetuximab) (un-)labeled with Yttrium-90 (90Y)). Tumors were excised 24 h post respective treatment. Residual DNA double strand breaks (DSB), mRNA expression of DNA damage response related genes, immunoblotting, tumor histology, and immunohistological staining were analyzed. An increase in number and complexity of residual DNA DSB was observed in FaDuDD tumors exposed to the combination treatment of external irradiation and 90Y-Cetuximab relative to controls. The increase was observed in a low oxygenated area, suggesting the expansion of DNA DSB damages. Upregulation of genes encoding p21cip1/waf1 (CDKN1A) and GADD45α (GADD45A) was determined in the combination treatment group, and immunoblotting as well as immunohistochemistry confirmed the upregulation of p21cip1/waf1. The increase in residual γH2AX foci leads to the blockage of cell cycle transition and subsequently to cell death, which could be observed in the upregulation of p21cip1/waf1 expression and an elevated number of cleaved caspase-3 positive cells. Overall, a complex interplay between DNA damage repair and programmed cell death accounts for the potential benefit of the combination therapy using 90Y-Cetuximab and external radiotherapy.
DOI:doi:10.3390/cancers13225595
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/10.3390/cancers13225595
 Volltext: https://www.mdpi.com/2072-6694/13/22/5595
 DOI: https://doi.org/10.3390/cancers13225595
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:cell death induction
 Cetuximab
 DNA damage response
 external beam radiotherapy
 molecular targeted radiotherapy
K10plus-PPN:1787219496
Verknüpfungen:→ Zeitschrift

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