دورية أكاديمية

Oncotarget / Hepatocyte specific expression of an oncogenic variant of β-catenin results in lethal metabolic dysfunction in mice

التفاصيل البيبلوغرافية
العنوان: Oncotarget / Hepatocyte specific expression of an oncogenic variant of β-catenin results in lethal metabolic dysfunction in mice
المؤلفون: Lemberger, Ursula J., Fuchs, Claudia D., Schöfer, Christian, Bileck, Andrea, Gerner, Christopher, Stojakovic, Tatjana, Taketo, Makoto M., Trauner, Michael, Egger, Gerda, Österreicher, Christoph H.
بيانات النشر: Impact Journals
سنة النشر: 2018
المجموعة: MedUni Vienna ePub (Medzinische Universität Wien)
مصطلحات موضوعية: Wnt signaling pathway, liver cancer, lipid metabolism, glucose metabolism, mitochondrial disorder
جغرافية الموضوع: UMW:14605, UMW:14574, UMW:14489
الوصف: Background: Wnt/β-catenin signaling plays a crucial role in embryogenesis, tissue homeostasis, metabolism and malignant transformation of different organs including the liver. Continuous β-catenin signaling due to somatic mutations in exon 3 of the Ctnnb1 gene is associated with different liver diseases including cancer and cholestasis. Results: Expression of a degradation resistant form of β-catenin in hepatocytes resulted in 100% mortality within 31 days after birth. Ctnnb1CA hep mice were characterized by reduced body weight, significantly enlarged livers with hepatocellular fat accumulation around central veins and increased hepatic triglyceride content. Proteomics analysis using whole liver tissue revealed significant deregulation of proteins involved in fat, glucose and mitochondrial energy metabolism, which was also reflected in morphological anomalies of hepatocellular mitochondria. Key enzymes involved in transport and synthesis of fatty acids and cholesterol were significantly deregulated in livers of Ctnnb1CA hep mice. Furthermore, carbohydrate metabolism was substantially disturbed in mutant mice. Conclusion: Continuous β-catenin signaling in hepatocytes results in premature death due to severe disturbances of liver associated metabolic pathways and mitochondrial dysfunction. Methods: To investigate the influence of permanent β-catenin signaling on liver biology we analyzed mice with hepatocyte specific expression of a dominant stable form of β-catenin (Ctnnb1CA hep) and their WT littermates by serum biochemistry, histology, electron microscopy, mRNA profiling and proteomic analysis of the liver.
نوع الوثيقة: article in journal/newspaper
وصف الملف: text/html
اللغة: English
تدمد: 1949-2553
العلاقة: vignette : https://repositorium.meduniwien.ac.at/titlepage/urn/urn:nbn:at:at-ubmuw:3-10350/128Test; urn:nbn:at:at-ubmuw:3-10350; https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-10350Test; local:99145284496103331; system:AC15596154
DOI: 10.18632/oncotarget.24346
الإتاحة: https://doi.org/10.18632/oncotarget.24346Test
https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-10350Test
حقوق: cc-by_3
رقم الانضمام: edsbas.821F72BF
قاعدة البيانات: BASE
الوصف
تدمد:19492553
DOI:10.18632/oncotarget.24346