The recent development of dissolution dynamic nuclear polarization (DNP) gives NMR the sensitivity to follow metabolic processes in living systems with high temporal resolution. In this article, we apply dissolution DNP to study the metabolism of hyperpolarized U- super(13)C, super(2)H sub(7)-glucose in living, perfused human breast cancer cells. Spectrally selective pulses were used to maximize the signal of the main product, lactate, whilst preserving the glucose polarization; in this way, both C sub(1)-lactate and C sub(3)-lactate could be observed with high temporal resolution. The production of lactate by T47D breast cancer cells can be characterized by Michaelis-Menten-like kinetics, with K sub(m)=3.5 plus or minus 1.5mm and V sub(max)=34 plus or minus 4 fmol/cell/min. The high sensitivity of this method also allowed us to observe and quantify the glycolytic intermediates dihydroxyacetone phosphate and 3-phosphoglycerate. Even with the enhanced DNP signal, many other glycolytic intermediates could not be detected directly. Nevertheless, by applying saturation transfer methods, the glycolytic intermediates glucose-6-phosphate, fructose-6-phosphate, fructose-1,6-bisphosphate, glyceraldehyde-3-phosphate, phosphoenolpyruvate and pyruvate could be observed indirectly. This method shows great promise for the elucidation of the distinctive metabolism and metabolic control of cancer cells, suggesting multiple ways whereby hyperpolarized U- super(13)C, super(2)H sub(7)-glucose NMR could aid in the diagnosis and characterization of cancer in vivo. Copyright copyright 2013 John Wiley & Sons, Ltd. New ways of monitoring glycolytic processes in live breast cancer cell cultures based on perdeuterated hyperpolarized glucose are demonstrated (a). Lactate and other intermediates are then visible on T47D cells maintained viable in a custom-made continuous bioreactor (b). Metabolic characteristics of other 'invisible' intermediates can also be gathered from saturation transfer experiments (c).