| Literature DB >> 31564440 |
Kristin L Granlund1, Sui-Seng Tee1, Hebert A Vargas2, Serge K Lyashchenko3, Ed Reznik4, Samson Fine5, Vincent Laudone6, James A Eastham6, Karim A Touijer6, Victor E Reuter5, Mithat Gonen4, Ramon E Sosa2, Duane Nicholson2, YanWei W Guo2, Albert P Chen7, James Tropp8, Fraser Robb9, Hedvig Hricak10, Kayvan R Keshari11.
Abstract
Metabolic imaging using hyperpolarized magnetic resonance can increase the sensitivity of MRI, though its ability to inform on relevant changes to biochemistry in humans remains unclear. In this work, we image pyruvate metabolism in patients, assessing the reproducibility of delivery and conversion in the setting of primary prostate cancer. We show that the time to max of pyruvate does not vary significantly within patients undergoing two separate injections or across patients. Furthermore, we show that lactate increases with Gleason grade. RNA sequencing data demonstrate a significant increase in the predominant pyruvate uptake transporter, monocarboxylate transporter 1. Increased protein expression was also observed in regions of high lactate signal, implicating it as the driver of lactate signal in vivo. Targeted DNA sequencing for actionable mutations revealed the highest lactate occurred in patients with PTEN loss. This work identifies a potential link between actionable genomic alterations and metabolic information derived from hyperpolarized pyruvate MRI.Entities:
Keywords: glycolytic flux; hyperpolarized pyruvate; in vivo kinetics; metabolic imaging
Year: 2019 PMID: 31564440 PMCID: PMC6949382 DOI: 10.1016/j.cmet.2019.08.024
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287