TY - JOUR
T1 - Hyperpolarized MRI visualizes Warburg effects and predicts treatment response to mTOR inhibitors in patient-derived CCRCC xenograft models
AU - Dong, Yiyu
AU - Eskandari, Roozbeh
AU - Ray, Chelsea
AU - Granlund, Kristin L.
AU - Santos-Cunha, Lidia Dos
AU - Miloushev, Vesselin Z.
AU - Tee, Sui Seng
AU - Jeong, Sangmoo
AU - Aras, Omer
AU - Chen, Ying Bei
AU - Cheng, Emily H.
AU - Hsieh, James J.
AU - Keshari, Kayvan R.
N1 - Funding Information:
This work was supported by the NIH, R01 CA223231 (Y. Dong, C. Ray, E.H. Cheng, and J.J. Hsieh), P30 CA008748 (K.R. Keshari), R00 EB014328 (K.R. Keshari), R01 CA195476 (K.R. Keshari) and R21 CA212958 (K.R. Keshari), K99 CA226357 (S. Jeong), as well as the Society of Memorial Sloan Kettering (Y.-B. Chen), the Center for Molecular Imaging and Nanotechnology (K.R. Keshari), and the Geoffrey Beene Cancer Research Center (K.R. Keshari). K.R. Keshari also serves on the SAB of NVision Imaging Technologies.
Publisher Copyright:
© 2019 American Association for Cancer Research.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - The ever-changing tumor microenvironment constantly challenges individual cancer cells to balance supply and demand, presenting tumor vulnerabilities and therapeutic opportunities. Everolimus and temsirolimus are inhibitors of mTOR (mTORi) approved for treating metastatic renal cell carcinoma (mRCC). However, treatment outcome varies greatly among patients. Accordingly, administration of mTORi in mRCC is diminishing, which could potentially result in missing timely delivery of effective treatment for select patients. Here, we implemented a clinically applicable, integrated platform encompassing a single dose of [1-13C] pyruvate to visualize the in vivo effect of mTORi on the conversion of pyruvate to lactate using hyperpolarized MRI. A striking difference that predicts treatment benefit was demonstrated using two preclinical models derived from patients with clear cell RCC (ccRCC) who exhibited primary resistance to VEGFRi and quickly succumbed to their diseases within 6 months after the diagnosis of metastasis without receiving mTORi. Our findings suggest that hyperpolarized MRI could be further developed to personalize kidney cancer treatment. Significance: These findings demonstrate hyperpolarized [1-13C]pyruvate MRI as a tool for accurately assessing the clinical success of mTOR inhibition in patients with ccRCC.
AB - The ever-changing tumor microenvironment constantly challenges individual cancer cells to balance supply and demand, presenting tumor vulnerabilities and therapeutic opportunities. Everolimus and temsirolimus are inhibitors of mTOR (mTORi) approved for treating metastatic renal cell carcinoma (mRCC). However, treatment outcome varies greatly among patients. Accordingly, administration of mTORi in mRCC is diminishing, which could potentially result in missing timely delivery of effective treatment for select patients. Here, we implemented a clinically applicable, integrated platform encompassing a single dose of [1-13C] pyruvate to visualize the in vivo effect of mTORi on the conversion of pyruvate to lactate using hyperpolarized MRI. A striking difference that predicts treatment benefit was demonstrated using two preclinical models derived from patients with clear cell RCC (ccRCC) who exhibited primary resistance to VEGFRi and quickly succumbed to their diseases within 6 months after the diagnosis of metastasis without receiving mTORi. Our findings suggest that hyperpolarized MRI could be further developed to personalize kidney cancer treatment. Significance: These findings demonstrate hyperpolarized [1-13C]pyruvate MRI as a tool for accurately assessing the clinical success of mTOR inhibition in patients with ccRCC.
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U2 - 10.1158/0008-5472.CAN-18-2231
DO - 10.1158/0008-5472.CAN-18-2231
M3 - Article
C2 - 30459151
AN - SCOPUS:85059448157
SN - 0008-5472
VL - 79
SP - 242
EP - 250
JO - Cancer research
JF - Cancer research
IS - 1
ER -