TY - JOUR
T1 - Real-time quantitative analysis of metabolic flux in live cells using a hyperpolarized micromagnetic resonance spectrometer
AU - Jeong, Sangmoo
AU - Eskandari, Roozbeh
AU - Park, Sun Mi
AU - Alvarez, Julio
AU - Tee, Sui Seng
AU - Weissleder, Ralph
AU - Kharas, Michael G.
AU - Lee, Hakho
AU - Keshari, Kayvan R.
N1 - Funding Information:
We thank V. Di Gialleonardo and L. Salamanca-Cardona for helping with the Western blot analysis and providing insightful comments on experimental details. This work was supported in part by U.S. NIH grants R01HL113156 (H.L.), R21CA205322 (H.L.), R00EB014328 (K.R.K.), and R21CA212958-01 (K.R.K.); Cancer Center Support Grant P30CA008748 (K.R.K.); and Department of Defense Ovarian Cancer Research Program Award W81XWH-14-1-0279 (H.L.) as well as the Center for Molecular Imaging and Nanotechnology at MSKCC.
Publisher Copyright:
Copyright © 2017 The Authors, some rights reserved.
PY - 2017/6
Y1 - 2017/6
N2 - Metabolic reprogramming is widely considered a hallmark of cancer, and understanding metabolic dynamics described by the conversion rates or “fluxes” of metabolites can shed light onto biological processes of tumorigenesis and response to therapy. For real-time analysis of metabolic flux in intact cells or organisms, magnetic resonance (MR) spectroscopy and imaging methods have been developed in conjunction with hyperpolarization of nuclear spins. These approaches enable noninvasive monitoring of tumor progression and treatment efficacy and are being tested in multiple clinical trials. However, because of their limited sensitivity, these methods require a larger number of cells, on the order of 107, which is impractical for analyzing scant target cells or mass-limited samples. We present a new technology platform, a hyperpolarized micromagnetic resonance spectrometer (HMRS), that achieves real-time, 103-fold more sensitive metabolic analysis on live cells. This platform enables quantification of the metabolic flux in a wide range of cell types, including leukemia stem cells, without significant changes in viability, which allows downstream molecular analyses in tandem. It also enables rapid assessment of metabolic changes by a given drug, which may direct therapeutic choices in patients. We further advanced this platform for high-throughput analysis of hyperpolarized molecules by integrating a three-dimensionally printed microfluidic system. The HMRS platform holds promise as a sensitive method for studying metabolic dynamics in mass-limited samples, including primary cancer cells, providing novel therapeutic targets and an enhanced understanding of cellular metabolism.
AB - Metabolic reprogramming is widely considered a hallmark of cancer, and understanding metabolic dynamics described by the conversion rates or “fluxes” of metabolites can shed light onto biological processes of tumorigenesis and response to therapy. For real-time analysis of metabolic flux in intact cells or organisms, magnetic resonance (MR) spectroscopy and imaging methods have been developed in conjunction with hyperpolarization of nuclear spins. These approaches enable noninvasive monitoring of tumor progression and treatment efficacy and are being tested in multiple clinical trials. However, because of their limited sensitivity, these methods require a larger number of cells, on the order of 107, which is impractical for analyzing scant target cells or mass-limited samples. We present a new technology platform, a hyperpolarized micromagnetic resonance spectrometer (HMRS), that achieves real-time, 103-fold more sensitive metabolic analysis on live cells. This platform enables quantification of the metabolic flux in a wide range of cell types, including leukemia stem cells, without significant changes in viability, which allows downstream molecular analyses in tandem. It also enables rapid assessment of metabolic changes by a given drug, which may direct therapeutic choices in patients. We further advanced this platform for high-throughput analysis of hyperpolarized molecules by integrating a three-dimensionally printed microfluidic system. The HMRS platform holds promise as a sensitive method for studying metabolic dynamics in mass-limited samples, including primary cancer cells, providing novel therapeutic targets and an enhanced understanding of cellular metabolism.
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U2 - 10.1126/sciadv.1700341
DO - 10.1126/sciadv.1700341
M3 - Article
C2 - 28630930
AN - SCOPUS:85041747594
SN - 2375-2548
VL - 3
JO - Science advances
JF - Science advances
IS - 6
M1 - e1700341
ER -