| Literature DB >> 30459151 |
Yiyu Dong1, Roozbeh Eskandari2,3, Chelsea Ray1, Kristin L Granlund2,3, Lidia Dos Santos-Cunha2,3, Vesselin Z Miloushev2,3, Sui Seng Tee2,3, Sangmoo Jeong2,3, Omer Aras2, Ying-Bei Chen4, Emily H Cheng1,4, James J Hsieh5, Kayvan R Keshari6,3,7.
Abstract
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. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 30459151 PMCID: PMC6318024 DOI: 10.1158/0008-5472.CAN-18-2231
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701