Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.

Real-time detection of the rates of metabolic flux, or exchange rates of endogenous enzymatic reactions, is now feasible in biological systems using Dynamic Nuclear Polarization Magnetic Resonance. Derivation of reaction rate kinetics from this technique typically requires multi-compartmental modeli...

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Main Authors: Deborah K Hill, Matthew R Orton, Erika Mariotti, Jessica K R Boult, Rafal Panek, Maysam Jafar, Harold G Parkes, Yann Jamin, Maria Falck Miniotis, Nada M S Al-Saffar, Mounia Beloueche-Babari, Simon P Robinson, Martin O Leach, Yuen-Li Chung, Thomas R Eykyn
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3762840?pdf=render
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spelling doaj-206e54d42db24a00bdc11c1c47e6760f2020-11-24T21:48:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7199610.1371/journal.pone.0071996Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.Deborah K HillMatthew R OrtonErika MariottiJessica K R BoultRafal PanekMaysam JafarHarold G ParkesYann JaminMaria Falck MiniotisNada M S Al-SaffarMounia Beloueche-BabariSimon P RobinsonMartin O LeachYuen-Li ChungThomas R EykynReal-time detection of the rates of metabolic flux, or exchange rates of endogenous enzymatic reactions, is now feasible in biological systems using Dynamic Nuclear Polarization Magnetic Resonance. Derivation of reaction rate kinetics from this technique typically requires multi-compartmental modeling of dynamic data, and results are therefore model-dependent and prone to misinterpretation. We present a model-free formulism based on the ratio of total areas under the curve (AUC) of the injected and product metabolite, for example pyruvate and lactate. A theoretical framework to support this novel analysis approach is described, and demonstrates that the AUC ratio is proportional to the forward rate constant k. We show that the model-free approach strongly correlates with k for whole cell in vitro experiments across a range of cancer cell lines, and detects response in cells treated with the pan-class I PI3K inhibitor GDC-0941 with comparable or greater sensitivity. The same result is seen in vivo with tumor xenograft-bearing mice, in control tumors and following drug treatment with dichloroacetate. An important finding is that the area under the curve is independent of both the input function and of any other metabolic pathways arising from the injected metabolite. This model-free approach provides a robust and clinically relevant alternative to kinetic model-based rate measurements in the clinical translation of hyperpolarized (13)C metabolic imaging in humans, where measurement of the input function can be problematic.http://europepmc.org/articles/PMC3762840?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Deborah K Hill
Matthew R Orton
Erika Mariotti
Jessica K R Boult
Rafal Panek
Maysam Jafar
Harold G Parkes
Yann Jamin
Maria Falck Miniotis
Nada M S Al-Saffar
Mounia Beloueche-Babari
Simon P Robinson
Martin O Leach
Yuen-Li Chung
Thomas R Eykyn
spellingShingle Deborah K Hill
Matthew R Orton
Erika Mariotti
Jessica K R Boult
Rafal Panek
Maysam Jafar
Harold G Parkes
Yann Jamin
Maria Falck Miniotis
Nada M S Al-Saffar
Mounia Beloueche-Babari
Simon P Robinson
Martin O Leach
Yuen-Li Chung
Thomas R Eykyn
Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.
PLoS ONE
author_facet Deborah K Hill
Matthew R Orton
Erika Mariotti
Jessica K R Boult
Rafal Panek
Maysam Jafar
Harold G Parkes
Yann Jamin
Maria Falck Miniotis
Nada M S Al-Saffar
Mounia Beloueche-Babari
Simon P Robinson
Martin O Leach
Yuen-Li Chung
Thomas R Eykyn
author_sort Deborah K Hill
title Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.
title_short Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.
title_full Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.
title_fullStr Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.
title_full_unstemmed Model free approach to kinetic analysis of real-time hyperpolarized 13C magnetic resonance spectroscopy data.
title_sort model free approach to kinetic analysis of real-time hyperpolarized 13c magnetic resonance spectroscopy data.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Real-time detection of the rates of metabolic flux, or exchange rates of endogenous enzymatic reactions, is now feasible in biological systems using Dynamic Nuclear Polarization Magnetic Resonance. Derivation of reaction rate kinetics from this technique typically requires multi-compartmental modeling of dynamic data, and results are therefore model-dependent and prone to misinterpretation. We present a model-free formulism based on the ratio of total areas under the curve (AUC) of the injected and product metabolite, for example pyruvate and lactate. A theoretical framework to support this novel analysis approach is described, and demonstrates that the AUC ratio is proportional to the forward rate constant k. We show that the model-free approach strongly correlates with k for whole cell in vitro experiments across a range of cancer cell lines, and detects response in cells treated with the pan-class I PI3K inhibitor GDC-0941 with comparable or greater sensitivity. The same result is seen in vivo with tumor xenograft-bearing mice, in control tumors and following drug treatment with dichloroacetate. An important finding is that the area under the curve is independent of both the input function and of any other metabolic pathways arising from the injected metabolite. This model-free approach provides a robust and clinically relevant alternative to kinetic model-based rate measurements in the clinical translation of hyperpolarized (13)C metabolic imaging in humans, where measurement of the input function can be problematic.
url http://europepmc.org/articles/PMC3762840?pdf=render
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