The lack of information regarding the metabolism and pathophysiology of ind
ividual tumors limits, in part, both the development of new anti-cancer the
rapies and the optimal implementation of currently available treatments. Ma
gnetic resonance [MR, including magnetic resonance imaging (MRI), magnetic
resonance spectroscopy (MRS), and electron paramagnetic resonance (EPR)] pr
ovides a powerful tool to assess many aspects of tumor metabolism and patho
physiology, Moreover, since this information can be obtained nondestructive
ly, pre-clinical results from cellular or animal models are often easily tr
anslated into the clinic. This review presents selected examples of how MR
has been used to identify metabolic changes associated with apoptosis, dete
ct therapeutic response prior to a change in tumor volume, optimize the com
bination of metabolic inhibitors with chemotherapy and/or radiation, charac
terize and exploit the influence of tumor pH on the effectiveness of chemot
herapy, characterize tumor reoxygenation and the effects of modifiers of tu
mor oxygenation in individual tumors, image transgene expression and assess
the efficacy of gene therapy,These examples provide an overview of several
of the areas In which cellular and animal model studies using MR have cont
ributed to our understanding of the effects of treatment on tumor metabolis
m and pathophysiology and the importance of tumor metabolism and pathophysi
ology as determinants of therapeutic response.