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The biology of cancer: metabolic reprogramming fuels cell growth and proliferation

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TLDR
This review examines the idea that several core fluxes, including aerobic glycolysis, de novo lipid biosynthesis, and glutamine-dependent anaplerosis, form a stereotyped platform supporting proliferation of diverse cell types and regulates regulation of these fluxes by cellular mediators of signal transduction and gene expression.
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This article is published in Cell Metabolism.The article was published on 2008-01-01 and is currently open access. It has received 3526 citations till now. The article focuses on the topics: PI3K/AKT/mTOR pathway & Lipid biosynthesis.

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Beyond EGFR inhibition: multilateral combat strategies to stop the progression of head and neck cancer

TL;DR: Recent multilateral efforts to discover and validate actionable strategies that involve signaling pathways in heterogenous head and neck cancer and to overcome anti-EGFR resistance in the era of precision medicine are discussed.
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Targeting T Cell Metabolism for Improvement of Cancer Immunotherapy.

TL;DR: The importance of metabolism on the function of tumor-associated immune cells is highlighted and the role of key metabolic determinants that might be targets of therapeutic intervention for improvement of tumor immunotherapies are addressed.
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The oncogenic transcription factor c-Jun regulates glutaminase expression and sensitizes cells to glutaminase-targeted therapy

TL;DR: It is reported that the transcription factor c-Jun, product of the proto-oncogene JUN, is a key regulator of mitochondrial glutaminase (GLS) levels, and ectopic overexpression of c- Jun renders breast cancer cells dependent on GLS activity.
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Metabolic adaptation of cancer and immune cells mediated by hypoxia-inducible factors.

TL;DR: This review summarizes the current understanding of how HIFs modulate the metabolism of hypoxic cancer cells and immune cells, and how altered metabolism plays a role in cancer progression.
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The metabolic basis of kidney cancer

TL;DR: Understanding the metabolic basis of kidney cancer will hopefully provide the foundation for the development of effective forms of therapy for this disease.
References
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Journal ArticleDOI

On the origin of cancer cells.

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Targeting HIF-1 for cancer therapy

TL;DR: Hypoxia-inducible factor 1 (HIF-1) activates the transcription of genes that are involved in crucial aspects of cancer biology, including angiogenesis, cell survival, glucose metabolism and invasion.
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HIF-1-mediated expression of pyruvate dehydrogenase kinase: A metabolic switch required for cellular adaptation to hypoxia

TL;DR: A hypoxia-induced metabolic switch that shunts glucose metabolites from the mitochondria to glycolysis to maintain ATP production and to prevent toxic ROS production is revealed.