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Status: Bibliographieeintrag

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Verfasst von:Turkowski, Kati [VerfasserIn]   i
 Herzberg, Frederik [VerfasserIn]   i
 Günther, Stefan [VerfasserIn]   i
 Brunn, David [VerfasserIn]   i
 Weigert, Andreas [VerfasserIn]   i
 Meister, Michael [VerfasserIn]   i
 Muley, Thomas [VerfasserIn]   i
 Kriegsmann, Mark [VerfasserIn]   i
 Schneider, Marc [VerfasserIn]   i
 Winter, Hauke [VerfasserIn]   i
 Thomas, Michael [VerfasserIn]   i
 Grimminger, Friedrich [VerfasserIn]   i
 Seeger, Werner [VerfasserIn]   i
 Savai Pullamsetti, Soni [VerfasserIn]   i
 Savai, Rajkumar [VerfasserIn]   i
Titel:Fibroblast growth factor-14 acts as tumor suppressor in lung adenocarcinomas
Verf.angabe:Kati Turkowski, Frederik Herzberg, Stefan Günther, David Brunn, Andreas Weigert, Michael Meister, Thomas Muley, Mark Kriegsmann, Marc A. Schneider, Hauke Winter, Michael Thomas, Friedrich Grimminger, Werner Seeger, Soni Savai Pullamsetti and Rajkumar Savai
E-Jahr:2020
Jahr:22 July 2020
Umfang:19 S.
Fussnoten:Gesehen am 22.10.2020
Titel Quelle:Enthalten in: Cells
Ort Quelle:Basel : MDPI, 2012
Jahr Quelle:2020
Band/Heft Quelle:9(2020,8) Artikel-Nummer 1755, 19 Seiten
ISSN Quelle:2073-4409
Abstract:Investigation of the molecular dynamics in lung cancer is crucial for the development of new treatment strategies. Fibroblast growth factor (FGF) 14 belongs to the FGF family, which might play a crucial role in cancer progression. We analyzed lung adenocarcinoma (LUAC) patients samples and found that FGF14 was downregulated, correlating with reduced survival and oncogenic mutation status. FGF14 overexpression in lung cancer cell lines resulted in decreased proliferation, colony formation, and migration, as well as increased expression of epithelial markers and a decreased expression of mesenchymal markers, indicating a mesenchymal to epithelial transition in vitro. We verified these findings using small interfering RNA against FGF14 and further confirmed the suppressive effect of FGF14 in a NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ immunodeficient xenograft tumor model. Moreover, FGF14 overexpressing tumor cell RNA sequencing data suggests that genes affected by FGF14 were related to the extracellular matrix, playing a role in proliferation and migration. Notably, newly identified FGF14 target genes, adenosine deaminase RNA specific B1 (ADARB1), collagen and calcium-binding epidermal growth factor domain-containing protein 1 (CCBE1), α1 chain of collagen XI (COL11A1), and mucin 16 (MUC16) expression was negatively correlated with overall survival when FGF14 was downregulated in LUAC. These findings led us to suggest that FGF14 regulates proliferation and migration in LUAC.
DOI:doi:10.3390/cells9081755
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/cells9081755
 Volltext: https://www.mdpi.com/2073-4409/9/8/1755
 DOI: https://doi.org/10.3390/cells9081755
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:fibroblast growth factor 14
 lung adenocarcinoma
 lung cancer mesenchymal epithelial transition
 xenograft model
K10plus-PPN:1736267906
Verknüpfungen:→ Zeitschrift

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