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      Inhibition of Fatty Acid Synthase Decreases Expression of Stemness Markers in Glioma Stem Cells

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          Abstract

          Cellular metabolic changes, especially to lipid metabolism, have recently been recognized as a hallmark of various cancer cells. However, little is known about the significance of cellular lipid metabolism in the regulation of biological activity of glioma stem cells (GSCs). In this study, we examined the expression and role of fatty acid synthase (FASN), a key lipogenic enzyme, in GSCs. In the de novo lipid synthesis assay, GSCs exhibited higher lipogenesis than differentiated non-GSCs. Western blot and immunocytochemical analyses revealed that FASN is strongly expressed in multiple lines of patient-derived GSCs (G144 and Y10), but its expression was markedly reduced upon differentiation. When GSCs were treated with 20 μM cerulenin, a pharmacological inhibitor of FASN, their proliferation and migration were significantly suppressed and de novo lipogenesis decreased. Furthermore, following cerulenin treatment, expression of the GSC markers nestin, Sox2 and fatty acid binding protein (FABP7), markers of GCSs, decreased while that of glial fibrillary acidic protein (GFAP) expression increased. Taken together, our results indicate that FASN plays a pivotal role in the maintenance of GSC stemness, and FASN-mediated de novo lipid biosynthesis is closely associated with tumor growth and invasion in glioblastoma.

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          Most cited references26

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          On the origin of cancer cells.

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            A rapid method of total lipid extraction and purification.

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              Monoacylglycerol lipase regulates a fatty acid network that promotes cancer pathogenesis.

              Tumor cells display progressive changes in metabolism that correlate with malignancy, including development of a lipogenic phenotype. How stored fats are liberated and remodeled to support cancer pathogenesis, however, remains unknown. Here, we show that the enzyme monoacylglycerol lipase (MAGL) is highly expressed in aggressive human cancer cells and primary tumors, where it regulates a fatty acid network enriched in oncogenic signaling lipids that promotes migration, invasion, survival, and in vivo tumor growth. Overexpression of MAGL in nonaggressive cancer cells recapitulates this fatty acid network and increases their pathogenicity-phenotypes that are reversed by an MAGL inhibitor. Impairments in MAGL-dependent tumor growth are rescued by a high-fat diet, indicating that exogenous sources of fatty acids can contribute to malignancy in cancers lacking MAGL activity. Together, these findings reveal how cancer cells can co-opt a lipolytic enzyme to translate their lipogenic state into an array of protumorigenic signals. PAPERFLICK:
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                25 January 2016
                2016
                : 11
                : 1
                : e0147717
                Affiliations
                [1 ]Department of Organ Anatomy, Yamaguchi University Graduate School of Medicine, Ube, Japan
                [2 ]Department of Neurosurgery, Yamaguchi University Graduate School of Medicine, Ube, Japan
                [3 ]Department of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan
                Wayne State University, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: Y. Yasumoto MS YO. Performed the experiments: Y. Yasumoto HM YK. Analyzed the data: Y. Yasumoto LKV MO YK. Contributed reagents/materials/analysis tools: Y. Yasumoto HS ME Y. Yamamoto. Wrote the paper: Y. Yasumoto YO.

                Article
                PONE-D-15-40519
                10.1371/journal.pone.0147717
                4726602
                26808816
                bf9fe1db-13eb-443a-a04e-d3921afad9c2
                © 2016 Yasumoto et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 15 September 2015
                : 13 December 2015
                Page count
                Figures: 5, Tables: 0, Pages: 14
                Funding
                The authors have no support or funding to report.
                Categories
                Research Article
                Biology and Life Sciences
                Biochemistry
                Lipids
                Fatty Acids
                Biology and Life Sciences
                Biochemistry
                Metabolism
                Lipogenesis
                Medicine and Health Sciences
                Oncology
                Cancers and Neoplasms
                Neurological Tumors
                Glioma
                Medicine and Health Sciences
                Neurology
                Neurological Tumors
                Glioma
                Biology and Life Sciences
                Biochemistry
                Lipids
                Biology and Life Sciences
                Biochemistry
                Proteins
                Cytoskeletal Proteins
                Nestin
                Medicine and Health Sciences
                Oncology
                Cancers and Neoplasms
                Blastomas
                Glioblastoma Multiforme
                Medicine and Health Sciences
                Oncology
                Cancers and Neoplasms
                Neurological Tumors
                Glioblastoma Multiforme
                Medicine and Health Sciences
                Neurology
                Neurological Tumors
                Glioblastoma Multiforme
                Research and Analysis Methods
                Biological Cultures
                Cell Cultures
                Cultured Tumor Cells
                Glioma Cells
                Biology and Life Sciences
                Biochemistry
                Enzymology
                Enzyme Chemistry
                Enzyme Metabolism
                Custom metadata
                All relevant data are within the paper and its Supporting Information files.

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                Uncategorized

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