دورية أكاديمية

Mitochondrial oxidative metabolism contributes to a cancer stem cell phenotype in cholangiocarcinoma

التفاصيل البيبلوغرافية
العنوان: Mitochondrial oxidative metabolism contributes to a cancer stem cell phenotype in cholangiocarcinoma
المؤلفون: Raggi, Chiara, Taddei, Maria Letizia, Sacco, Elena, Navari, Nadia, Correnti, Margherita, Piombanti, Benedetta, Pastore, Mirella, Campani, Claudia, Pranzini, Erica, Iorio, Jessica, Lori, Giulia, Lottini, Tiziano, Peano, Clelia, Cibella, Javier, Lewinska, Monika, Andersen, Jesper B, di Tommaso, Luca, Vigano, Luca, Di Maira, Giovanni, Madiai, Stefania, Ramazzotti, Matteo, Orlandi, Ivan, Arcangeli, Annarosa, Chiarugi, Paola, Marra, Fabio
المساهمون: C. Raggi, M.L. Taddei, E. Sacco, N. Navari, M. Correnti, B. Piombanti, M. Pastore, C. Campani, E. Pranzini, J. Iorio, G. Lori, T. Lottini, C. Peano, J. Cibella, M. Lewinska, J.B. Andersen, L. di Tommaso, L. Vigano, G. Di Maira, S. Madiai, M. Ramazzotti, I. Orlandi, A. Arcangeli, P. Chiarugi, F. Marra
بيانات النشر: Elsevier
سنة النشر: 2021
المجموعة: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
مصطلحات موضوعية: CCLP1, HUCCT1, OXPHOS, PGC-1α, SR-18292, Settore BIO/11 - Biologia Molecolare, Settore MED/04 - Patologia Generale
الوصف: BACKGROUND AND AIMS: Little is known about the metabolic regulation of cancer stem cells (CSC) in cholangiocarcinoma (CCA). We analyzed whether mitochondrial-dependent metabolism and related signaling pathways contribute to stem state in CCA.METHODS: The stem-like subset was enriched by sphere culture (SPH) in human intrahepatic CCA cells (HUCCT1 and CCLP1) and compared to cells cultured in monolayer. Extracellular flux analysis was examined by Seahorse technology and high-resolution respirometry. In patients with CCA, expression of factors related to mitochondrial metabolism was analyzed for possible correlation with clinical parameters.RESULTS: Metabolic analyses revealed a more efficient respiratory phenotype in CCA-SPH than in monolayers, due to mitochondrial oxidative phosphorylation. CCA-SPH showed high mitochondrial membrane potential and elevated mitochondrial mass, and over-expressed peroxisome proliferator-activated receptor gamma coactivator (PGC)-1alpha, a master regulator of mitochondrial biogenesis. Targeting mitochondrial complex I in CCA-SPH by metformin, or PGC-1alpha silencing or pharmacologic inhibition (SR-18292) impaired spherogenicity and expression of markers related to the CSC phenotype, pluripotency, and epithelial-mesenchymal transition. In mice with tumor xenografts generated by injection of CCA-SPH, administration of metformin or SR-18292 significantly reduced tumor growth and determined a phenotype more similar to tumors originated from cells grown in monolayer. In CCA patients, expression of PGC-1alpha was correlated to expression of mitochondrial complex II and of stem-like genes. Patients with higher PGC-1alpha expression by immunostaining had lower overall survival (OS) and progression-free survival, higher angioinvasion and faster recurrence. In GSEA analysis, CCA patients with high levels of mitochondrial Complex II had shorter OS and time to recurrence.CONCLUSIONS: The CCA stem-subset has a more efficient respiratory phenotype and depends on mitochondrial oxidative metabolism ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33484774; info:eu-repo/semantics/altIdentifier/wos/WOS:000514835500084; numberofpages:14; journal:JOURNAL OF HEPATOLOGY; http://hdl.handle.net/2434/825203Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85104152123
DOI: 10.1016/j.jhep.2020.12.031
الإتاحة: https://doi.org/10.1016/j.jhep.2020.12.031Test
http://hdl.handle.net/2434/825203Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.2E720197
قاعدة البيانات: BASE