Gliomas maintain an acidic extracellular pH (pH e ), which promotes tumor growth and builds resistance to therapy. Given evidence that acidic pH e beyond the tumor core indicates infiltration, we hypothesized that imaging the intratumoral pH e in relation to the peritumoral pH e can provide a novel readout of therapeutic influence on the tumor microenvironment. We used Biosensor Imaging of Redundant Deviation in Shifts (BIRDS), which utilizes chemical shifts of non-exchangeable protons from macrocyclic chelates (e.g., DOTP 8− ) complexed with paramagnetic thulium (Tm 3+ ), to generate pH e maps in rat brains bearing U251 tumors. Following TmDOTP 5− infusion, T 2 -weighted MRI provided delineation of the tumor boundary and BIRDS was used to image the pH e gradient between intratumoral and peritumoral regions (ΔpH e ) in both untreated and temozolomide treated (40 mg/kg) rats bearing U251 tumors. Treated rats had reduced tumor volume (p < 0.01), reduced proliferation (Ki-67 staining; p < 0.03) and apoptosis induction (cleaved Caspase-3 staining; p < 0.001) when compared to untreated rats. The ΔpH e was significantly higher in untreated compared to treated rats (p < 0.002), suggesting that temozolomide, which induces apoptosis and hinders proliferation, also normalizes intratumoral pH e . Thus, BIRDS can be used to map the ΔpH e in gliomas and provide a physiological readout of the therapeutic response on the tumor microenvironment.
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Rao et al. (2017) studied this question.
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