- Open Access
Altered metabolism in cancer
© Locasale and Cantley; licensee BioMed Central Ltd. 2010
- Received: 28 May 2010
- Accepted: 22 June 2010
- Published: 25 June 2010
Cancer cells have different metabolic requirements from their normal counterparts. Understanding the consequences of this differential metabolism requires a detailed understanding of glucose metabolism and its relation to energy production in cancer cells. A recent study in BMC Systems Biology by Vasquez et al. developed a mathematical model to assess some features of this altered metabolism. Here, we take a broader look at the regulation of energy metabolism in cancer cells, considering their anabolic as well as catabolic needs.
See research article: http://0-www.biomedcentral.com.brum.beds.ac.uk/1752-0509/4/58/
- Krebs Cycle
- Aerobic Glycolysis
- Altered Metabolism
- Futile Cycle
- Pathway Flux
Catabolic pathways involving the oxidation of material other than glucose in the Krebs cycle are also involved in cancer cell metabolism. For example, glutamine flux into the Krebs cycle has been directly observed in cancer cell lines and appears to be in part regulated by expression of MYC and TP53 (p53) - two of the most common cancer-associated genes [4–6]. Additional amino acids such as arginine and glycine, and metabolic intermediates such as fatty acids, can also be metabolized by mitochondrial pathways in certain contexts. These metabolites have transporters to deliver them into cells and are present in sufficiently high plasma concentrations to support their use in catabolic metabolism in mitochondria . In addition, many of the anabolic products that stem from intermediates in glycolysis can ultimately flow into the Krebs cycle, resulting in a bypass of the generation of pyruvate - the end product of glycolysis. This type of glucose metabolism avoids metabolic activity involving pyruvate kinase and pyruvate dehydrogenase, which are typically inhibited in cancer cells . These alternative pathways present many opportunities for additional stages of regulation in the decision to commit carbon flux to anabolic versus catabolic metabolism, and more research is required to understand the origins and tumor specificities of Krebs cycle flux.
Aerobic glycolysis is considered a relatively inefficient way of producing ATP, as the alternative catabolic fate of glucose via oxidation in the Krebs cycle and donation of electrons into the electron-transport chain can generate 15 to 20 times as much ATP per unit of glucose. A recent study by Vazquez et al.  used a reduced flux-balance model to suggest that synthesizing ATP from glucose through aerobic glycolysis is the optimal ATP-generating strategy when a cell is limited by its capacity to maintain enough mitochondrial mass to support sufficient flux through the electron-transport chain. Whether fermentation is an optimal ATP-generating strategy is unclear; however, there are several lines of evidence that suggest that tumor cell proliferation is not limited by ATP availability.
From the equation, it is clear that glycolysis is not possible without sufficient regeneration of ADP and NAD+. The reduction of pyruvate to lactate by lactate dehydrogenase is the most ubiquitous mechanism known for converting NADH back to NAD+, and this activity balances the very high rate of glycolysis observed in most cancer cells. Efraim Racker noted the problem of stoichiometric ADP availability and postulated that large fluxes through yet to be characterized ATP-coupled hydrolysis reactions were required to balance the cellular glucose uptake rates found in tumors. Futile cycles, more conveniently directly coupled to glycolysis, that hydrolyze ATP were believed to be required to balance high glycolytic flux . One now established example of a futile cycle in glycolysis involves a shunting step in which fructose 6-phosphate (F6P) is phosphorylated to form fructose 2,6-bisphosphate, which is then dephosphorylated back to F6P, resulting in net ATP hydrolysis. Attention has recently been paid to the cancer specificity of these reactions and some studies suggest that the enzyme activity responsible may be differentially regulated in some cancers . Other ATP-consuming futile cycles in central carbon metabolism may yet be discovered.
Although aerobic glycolysis may, by virtue of stoichiometry, be necessary to support high rates of glycolysis, the advantages of this process for tumor cells are complicated to understand. Cell-autonomous effects of lactate secretion are likely to confer advantages on tumors. Lactate may enhance the invasiveness of tumor cells by disrupting normal tissue architecture as well as promoting an environment with reduced pH to evade tumor-attacking immune cells.
A complementary teleology suggests that maintaining high rates of glycolysis is required to reconfigure metabolic pathway fluxes to achieve more efficient anabolic metabolism and cell-autonomous growth. One speculation is that a movement of pathway fluxes towards anabolic metabolism can arise from the effects of differential ATP hydrolysis and redox balance that originate from the demands of the stoichiometry shown in the equation above. These differential pathway fluxes are likely to be dependent on tumor type since different oncogenes are used to regulate different anabolic fluxes.
Cancer cells are limited in their growth by the availability of carbon skeletons needed to produce new proteins, nucleotides and lipids . Furthermore, the reducing equivalents in the form of NADPH required for reductive biosynthesis derive from pathways that are orthogonal to ATP-generating pathways. Multiple solutions to the problem of obtaining sufficient carbon material and reducing equivalents are obtainable, and probably depend on the genetic context of the tumor and its microenvironment. A comprehensive understanding of how NADPH is generated and used in cells, and the predominant anabolic carbon fluxes stemming from glucose uptake, will help to parse the molecular consequences of aerobic glycolysis.
Because of the complexity of cancer metabolism, a better understanding will ultimately require the use of mathematical models. This improved understanding will then allow intervention in the metabolic pathways responsible for tumor cell metabolism. Exploiting these tumor-specific properties presents opportunities for therapeutic intervention in tumor development. The pharmacological targeting of enzymes that regulate this restructured metabolism has recently shown some promise in preclinical studies .
We would like to thank Cynthia Clower, Edouard Mullarky, Gina DeNicola, Matt Vander Heiden, Alex Grassian and Tamar Melman for helpful comments on the manuscript. JWL was supported by a fellowship from the American Cancer Society.
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