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Altered metabolism in cancer cells is pivotal for tumor growth, most notably by providing energy, reducing equivalents and building blocks while several metabolites exert a aling function promoting tumor growth and progression.

A cancer tissue cannot be simply reduced to a bulk of proliferating cells. Tumors Dating sites weird indeed complex How to start a convo with a girl on a dating website dynamic structures where single cells can heterogeneously perform various biological activities with different metabolic requirements. Because tumors are composed of different types of cells with metabolic activities affected by different spatial and temporal contexts, it is important to address metabolism taking into cellular and biological heterogeneity.

In this review, we describe this heterogeneity also in metabolic fluxes, thus showing the relative contribution of different metabolic activities to tumor progression according to the cellular context.

Highlights

View PDF Download full issue. Add to Mendeley Share. Under an Elsevier user. Abstract Altered metabolism in cancer cells is pivotal for tumor growth, most notably by providing energy, reducing equivalents and building blocks while several metabolites exert a aling function promoting tumor growth and progression. AMPK adenosine monophosphate kinase.

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ARG1 l -arginine-metabolizing enzyme arginase 1. BCAA branched-chain amino acid. Bcl2 B-cell lymphoma 2. CAF cancer-associated fibroblast.

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CIC cancer-initiating cell. COX2 cytochrome oxidase. CSC cancer stem cell.

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CREB cyclic adenosine monophosphate response element binding protein. DEC1 differentially expressed in chondrocytes 1. EMT epithelial-to-mesenchymal transition. FAK focal adhesion kinase. FAS fatty acid synthase.

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FBP fructose 1,6-bisphosphate. GAPDH glyceraldehydephosphate dehydrogenase. HIF-1 hypoxia-activated factor HK2 hexokinase 2.

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HMGB1 high-mobility group box 1. HUVEC human umbilical vein endothelial cell.

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LDH lactate dehydrogenase. MEF murine embryonic fibroblast. MET mesenchymal to epithelial transition.

Associated data

MRI magnetic resonance imaging. NSCLC non-small cell lung cancer.

PDAC pancreatic ductal adenocarcinoma. PHD prolylhydroxylase.

Associated data

PK pyruvate kinase. PPP pentose phosphate pathway. RhoA Ras homolog gene family, member A. ROS reactive oxygen species. SASP senescence-associated secretory phenotype. SCO2 synthesis of cytochrome oxidase 2.

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SGK-1 serum and glucocorticoid-regulated kinase-1 Sirt1, sirtuin 1. TAM tumor-associated macrophage.

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TSC2 tuberous sclerosis 2. VDAC voltage-dependent anion channel. VEGF vascular endothelial growth factor.

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ZEB Zinc finger E-box-binding homeobox. Keywords Cancer. Recommended articles Citing articles 0.