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Status: Bibliographieeintrag

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Verfasst von:Scherr, Anna-Lena [VerfasserIn]   i
 Jassowicz, Adam [VerfasserIn]   i
 Pató, Anna [VerfasserIn]   i
 Elßner, Christin [VerfasserIn]   i
 Ismail, Lars [VerfasserIn]   i
 Schmitt, Nathalie [VerfasserIn]   i
 Hoffmeister-Wittmann, Paula [VerfasserIn]   i
 Neukirch, Lasse [VerfasserIn]   i
 Gdynia, Georg [VerfasserIn]   i
 Goeppert, Benjamin [VerfasserIn]   i
 Schulze-Bergkamen, Henning [VerfasserIn]   i
 Jäger, Dirk [VerfasserIn]   i
 Köhler, Bruno Christian [VerfasserIn]   i
Titel:Knockdown of Atg7 induces nuclear-LC3 dependent apoptosis and augments chemotherapy in colorectal cancer cells
Verf.angabe:Anna-Lena Scherr, Adam Jassowicz, Anna Pató, Christin Elssner, Lars Ismail, Nathalie Schmitt, Paula Hoffmeister, Lasse Neukirch, Georg Gdynia, Benjamin Goeppert, Henning Schulze-Bergkamen, Dirk Jäger and Bruno Christian Köhler
E-Jahr:2020
Jahr:7 February 2020
Fussnoten:Gesehen am 13.05.2020
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2020
Band/Heft Quelle:21(2020,3) Artikel-Nummer 1099, 15 Seiten
ISSN Quelle:1422-0067
 1661-6596
Abstract:Autophagy is a catabolic process that enables cells to degrade obsolete content and refuel energy depots. In colorectal cancer (CRC) autophagy has been shown to promote tumorigenesis through energy delivery in the condition of uncontrolled proliferation. With this study, we aimed at evaluating whether autophagy sustains CRC cell viability and if it impacts therapy resistance. Initially, a colorectal cancer tissue micro array, containing mucosa (n = 10), adenoma (n = 18) and adenocarcinoma (n = 49) spots, was stained for expression of essential autophagy proteins LC3b, Atg7, p62 and Beclin-1. Subsequently, central autophagy proteins were downregulated in CRC cells using siRNA technology. Viability assays, flow cytometry and immunoblotting were performed and three-dimensional cell culture was utilized to study autophagy in a tissue mimicking environment. In our study we found an upregulation of Atg7 in CRC. Furthermore, we identified Atg7 as crucial factor within the autophagy network for CRC cell viability. Its disruption induced cell death via triggering apoptosis and in combination with conventional chemotherapy it exerted synergistic effects in inducing CRC cell death. Cell death was strictly dependent on nuclear LC3b, since simultaneous knockdown of Atg7 and LC3b completely restored viability. This study unravels a novel cell death preventing function of Atg7 in interaction with LC3b, thereby unmasking a promising therapeutic target in CRC.
DOI:doi:10.3390/ijms21031099
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/ijms21031099
 Volltext: https://www.mdpi.com/1422-0067/21/3/1099
 DOI: https://doi.org/10.3390/ijms21031099
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:apoptosis
 Atg7
 autophagy
 colorectal cancer
 LC3
K10plus-PPN:1698155808
Verknüpfungen:→ Zeitschrift

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