Metastasis of pancreatic cancer: An uninflamed liver micromilieu controls cell growth and cancer stem cell properties by oxidative phosphorylation in pancreatic ductal epithelial cells.

Fabian, Alexander; Stegner, Simon; Miarka, Lauritz; Zimmermann, Johannes; Lenk, Lennart; Rahn, Sascha; Buttlar, Jann; Viol, Fabrice; Knaack, Hendrike; Esser, Daniela; Schäuble, Sascha; Großmann, Peter; Marinos, Georgios; Häsler, Robert; Mikulits, Wolfgang; Saur, Dieter; Kaleta, Christoph; Schäfer, Heiner; Sebens, Susanne

doi:10.1016/j.canlet.2019.03.039

Lehrstuhl für Translationale Tumorforschung (DKTK) (Prof. Saur)

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Titel:: Metastasis of pancreatic cancer: An uninflamed liver micromilieu controls cell growth and cancer stem cell properties by oxidative phosphorylation in pancreatic ductal epithelial cells.
Dokumenttyp:: Journal Article; Research Support, Non-U.S. Gov't
Autor(en):: Fabian, Alexander; Stegner, Simon; Miarka, Lauritz; Zimmermann, Johannes; Lenk, Lennart; Rahn, Sascha; Buttlar, Jann; Viol, Fabrice; Knaack, Hendrike; Esser, Daniela; Schäuble, Sascha; Großmann, Peter; Marinos, Georgios; Häsler, Robert; Mikulits, Wolfgang; Saur, Dieter; Kaleta, Christoph; Schäfer, Heiner; Sebens, Susanne
Abstract:: Pancreatic ductal adenocarcinoma (PDAC) is commonly diagnosed when liver metastases already emerged. We recently demonstrated that hepatic stromal cells determine the dormancy status along with cancer stem cell (CSC) properties of pancreatic ductal epithelial cells (PDECs) during metastasis. This study investigated the influence of the hepatic microenvironment - and its inflammatory status - on metabolic alterations and how these impact cell growth and CSC-characteristics of PDECs. Coculture with hepatic stellate cells (HSCs), simulating a physiological liver stroma, but not with hepatic myofibroblasts (HMFs) representing liver inflammation promoted expression of Succinate Dehydrogenase subunit B (SDHB) and an oxidative metabolism along with a quiescent phenotype in PDECs. SiRNA-mediated SDHB knockdown increased cell growth and CSC-properties. Moreover, liver micrometastases of tumor bearing KPC mice strongly expressed SDHB while expression of the CSC-marker Nestin was exclusively found in macrometastases. Consistently, RNA-sequencing and in silico modeling revealed significantly altered metabolic fluxes and enhanced SDH activity predominantly in premalignant PDECs in the presence of HSC compared to HMF. Overall, these data emphasize that the hepatic microenvironment determines the metabolism of disseminated PDECs thereby controlling cell growth and CSC-properties during liver metastasis. «
Pancreatic ductal adenocarcinoma (PDAC) is commonly diagnosed when liver metastases already emerged. We recently demonstrated that hepatic stromal cells determine the dormancy status along with cancer stem cell (CSC) properties of pancreatic ductal epithelial cells (PDECs) during metastasis. This study investigated the influence of the hepatic microenvironment - and its inflammatory status - on metabolic alterations and how these impact cell growth and CSC-characteristics of PDECs. Coculture wit... »
Zeitschriftentitel:: Cancer Lett
Jahr:: 2019
Band / Volume:: 453
Seitenangaben Beitrag:: 95-106
Volltext / DOI:: doi:10.1016/j.canlet.2019.03.039
PubMed:: http://view.ncbi.nlm.nih.gov/pubmed/30930235
Print-ISSN:: 0304-3835
TUM Einrichtung:: Lehrstuhl für Experimentelle Tumortherapie (Prof. Saur)
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mediaTUM Gesamtbestand Einrichtungen Schools TUM School of Medicine and Health Departments Clinical Medicine Institut für Experimentelle Tumortherapie (Prof. Saur)Lehrstuhl für Translationale Tumorforschung (DKTK) (Prof. Saur)2019