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https://hdl.handle.net/20.500.14365/1081
Title: | Effect of Adipocyte-Secreted Factors on Epcam+/Cd133+hepatic Stem Cell Population | Authors: | Karagonlar, Zeynep Firtina Koc, Dogukan Sahin, Eren Avci, Sanem Tercan Yilmaz, Mustafa Atabey, Nese Erdal, Esra |
Keywords: | Adipocytes Cytokines HCC IL6 c-Met STAT3 Hepatocyte Growth-Factor Tumor-Initiating Cells Hepatocellular-Carcinoma Metabolic Syndrome Cancer Interleukin-6 Obesity Hepatocarcinogenesis Differentiation Expression |
Publisher: | Academic Press Inc Elsevier Science | Abstract: | Recent epidemiological studies have associated obesity with a variety of cancer types including HCC. However, the tumor initiating role of obesity in hepatocarcinogenesis is still unknown. The objective of this paper is to investigate the effect of adipocyte-secreted factors on EpCAM+/CD133+ cancer stern cells and to identify which factors play a role in modulating hepatic cancer stem cell behavior. Our results demonstrated that adipocyte-secreted factors affect motility and drug resistance of EpCAM+/CD133+ cells. When incubated with adipocyte conditioned media, EpCAM-F/CD133+ cells exhibited augmented motility and reduced sorafenib-induced apoptosis. Using array-based system, we identified secretion of several cytokines such as IL6, IL8 and MCP1 by cultured adipocytes and activation of c-Met, STAT3 and ERK1/2 signaling pathways in EpCAM-F/CD133+ cells incubated with adipocyte conditioned media. Treating EpCAM+/CD133+ cancer stem cells with IL6 receptor blocking antibody or c-Met inhibitor SU11274 both reduced the increase in motility; however SU11274 had greater effect on relieving protection from sorafenib-induced apoptosis. These results indicate that adipocyte-secreted factors might regulate cancer stem cell behavior through several signaling molecules including c-Met, STAT3 and ERK1/2 and inhibition of these signaling pathways offer novel strategies in targeting the effect of adipose derived cytokines in cancer. (C) 2016 Elsevier Inc. All rights reserved. | URI: | https://doi.org/10.1016/j.bbrc.2016.04.137 https://hdl.handle.net/20.500.14365/1081 |
ISSN: | 0006-291X 1090-2104 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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