It was established through in vivo T 1 measurements at lowm agnetic fields that tumour cells displayp roton T 1 values that are markedly longer than those shown by healthy tissue.M oreover,i th as been found that the elongation of T 1 parallels the aggressiveness of the investigated tumour.The T 1 lengthening is associated with an enhanced water exchange rate across the transcytolemmal membrane through an overexpression/upregulation of GLUT1 and Na + /K + ATPase transporters.I tf ollows that the intracellular water lifetime represents ah allmark of tumour cells that can be easily monitored by measuring T 1 at different magnetic field strengths ranging from 0.2 to 200 mT.Magnetic resonance imaging (MRI) has played ak ey role in the field of oncology over the last few decades.T he prominent role of MRI relies on its superb spatial and temporal resolution, and its diagnostic power basically arises from the differences in the longitudinal (T 1 )a nd transverse (T 2 )p roton relaxation times between healthy and pathological tissues.H owever, at the magnetic field strength of the currently available MRI scanners,changes in T 1 do not appear to be sensitive enough to report on the particular aspects of the tumour stage. [1] However,t here is widespread opinion that at low magnetic field strength, the marked increase in R 1 (= 1/T 1 )o bserved in biological tissues might be beneficial towards improving the MRI diagnostic potential in tumour phenotyping. [2] Herein, it is shown that the in vivo acquisition of 1/T 1 nuclear magnetic resonance dispersion (NMRD) profiles (from 0.2 to 200 mT) fully supports this expectation as the observed R 1 values at low magnetic fields (< 0.2 T) enable the clear discrimination between tumours characterised by different metastatic potentials.The1 / T 1 NMRD profiles were acquired on fast field cycling (FFC) relaxometers,w hich are able to switch the Figure 1. A) The FFC experiment:T he nuclear spin polarization is built up during the pre-polarization phase, at B p .R elaxation occurs during the evolution period (t)atB r ,t hen the NMR signal is detected at B d . The sequence is repeated,s taggering t each time. ForB r > 7MHz, the cycle starts in the absence of any polarization field. B) Photographs of the FFC-NMR relaxometer showing the introducedm odificationsfor the in vivo acquisition:a)the FFC magnet;b)the mouse holding system;c )the transmitter/receiver coil around the mouse'sl eg.