Gene Network Analysis of Glucose Linked Signaling Pathways and Their Role in Human Hepatocellular Carcinoma Cell Growth and Survival in HuH7 and HepG2 Cell LinesReportar como inadecuado




Gene Network Analysis of Glucose Linked Signaling Pathways and Their Role in Human Hepatocellular Carcinoma Cell Growth and Survival in HuH7 and HepG2 Cell Lines - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

BioMed Research International - Volume 2015 2015, Article ID 821761, 19 pages -

Research Article

Lyon University, INSERM, UMR1060, INRA1397, CarMeN Laboratory, INSA, HCL, 69008 Lyon, France

Lyon University, Centre de Génétique et de Physiologie Moléculaire et Cellulaire CGPhiMC, CNRS UMR5534, 69622 Lyon, France

Received 5 January 2015; Accepted 6 March 2015

Academic Editor: Ming Wu

Copyright © 2015 Emmanuelle Berger et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Cancer progression may be affected by metabolism. In this study, we aimed to analyze the effect of glucose on the proliferation and-or survival of human hepatocellular carcinoma HCC cells. Human gene datasets regulated by glucose were compared to gene datasets either dysregulated in HCC or regulated by other signaling pathways. Significant numbers of common genes suggested putative involvement in transcriptional regulations by glucose. Real-time proliferation assays using high 4.5 g-L versus low 1 g-L glucose on two human HCC cell lines and specific inhibitors of selected pathways were used for experimental validations. High glucose promoted HuH7 cell proliferation but not that of HepG2 cell line. Gene network analyses suggest that gene transcription by glucose could be mediated at 92% through ChREBP in HepG2 cells, compared to 40% in either other human cells or rodent healthy liver, with alteration of LKB1 serine-threonine kinase 11 and NOX NADPH oxidases signaling pathways and loss of transcriptional regulation of PPARGC1A peroxisome-proliferator activated receptors gamma coactivator 1 target genes by high glucose. Both PPARA and PPARGC1A regulate transcription of genes commonly regulated by glycolysis, by the antidiabetic agent metformin and by NOX, suggesting their major interplay in the control of HCC progression.





Autor: Emmanuelle Berger, Nathalie Vega, Michèle Weiss-Gayet, and Alain Géloën

Fuente: https://www.hindawi.com/



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