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Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy

While pancreatic cancer (PC) survival rates have recently shown modest improvement, the disease remains largely incurable. Early detection of pancreatic cancer may result in improved outcomes and therefore, methods for early detection of cancer, even premalignant lesions, may provide more favorable...

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Autores principales: Dutta, Prasanta, Castro Pando, Susana, Mascaro, Marilina, Riquelme, Erick, Zoltan, Michelle, Zacharias, Niki M., Gammon, Seth T., Piwnica-Worms, David, Pagel, Mark D., Sen, Subrata, Maitra, Anirban, Shams, Shayan, McAllister, Florencia, Bhattacharya, Pratip K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279395/
https://www.ncbi.nlm.nih.gov/pubmed/32466260
http://dx.doi.org/10.3390/ijms21103722
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author Dutta, Prasanta
Castro Pando, Susana
Mascaro, Marilina
Riquelme, Erick
Zoltan, Michelle
Zacharias, Niki M.
Gammon, Seth T.
Piwnica-Worms, David
Pagel, Mark D.
Sen, Subrata
Maitra, Anirban
Shams, Shayan
McAllister, Florencia
Bhattacharya, Pratip K.
author_facet Dutta, Prasanta
Castro Pando, Susana
Mascaro, Marilina
Riquelme, Erick
Zoltan, Michelle
Zacharias, Niki M.
Gammon, Seth T.
Piwnica-Worms, David
Pagel, Mark D.
Sen, Subrata
Maitra, Anirban
Shams, Shayan
McAllister, Florencia
Bhattacharya, Pratip K.
author_sort Dutta, Prasanta
collection PubMed
description While pancreatic cancer (PC) survival rates have recently shown modest improvement, the disease remains largely incurable. Early detection of pancreatic cancer may result in improved outcomes and therefore, methods for early detection of cancer, even premalignant lesions, may provide more favorable outcomes. Pancreatic intraepithelial neoplasias (PanINs) have been identified as premalignant precursor lesions to pancreatic cancer. However, conventional imaging methods used for screening high-risk populations do not have the sensitivity to detect PanINs. Here, we have employed hyperpolarized metabolic imaging in vivo and nuclear magnetic resonance ((1)H-NMR) metabolomics ex vivo to identify and understand metabolic changes, towards enabling detection of early PanINs and progression to advanced PanINs lesions that precede pancreatic cancer formation. Progression of disease from tissue containing predominantly low-grade PanINs to tissue with high-grade PanINs showed a decreasing alanine/lactate ratio from high-resolution NMR metabolomics ex vivo. Hyperpolarized magnetic resonance spectroscopy (HP-MRS) allows over 10,000-fold sensitivity enhancement relative to conventional magnetic resonance. Real-time HP-MRS was employed to measure non-invasively changes of alanine and lactate metabolites with disease progression and in control mice in vivo, following injection of hyperpolarized [1-(13)C] pyruvate. The alanine-to-lactate signal intensity ratio was found to decrease as the disease progressed from low-grade PanINs to high-grade PanINs. The biochemical changes of alanine transaminase (ALT) and lactate dehydrogenase (LDH) enzyme activity were assessed. These results demonstrate that there are significant alterations of ALT and LDH activities during the transformation from early to advanced PanINs lesions. Furthermore, we demonstrate that real-time conversion kinetic rate constants (k(PA) and k(PL)) can be used as metabolic imaging biomarkers of pancreatic premalignant lesions. Findings from this emerging HP-MRS technique can be translated to the clinic for detection of pancreatic premalignant lesion in high-risk populations.
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spelling pubmed-72793952020-06-17 Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy Dutta, Prasanta Castro Pando, Susana Mascaro, Marilina Riquelme, Erick Zoltan, Michelle Zacharias, Niki M. Gammon, Seth T. Piwnica-Worms, David Pagel, Mark D. Sen, Subrata Maitra, Anirban Shams, Shayan McAllister, Florencia Bhattacharya, Pratip K. Int J Mol Sci Article While pancreatic cancer (PC) survival rates have recently shown modest improvement, the disease remains largely incurable. Early detection of pancreatic cancer may result in improved outcomes and therefore, methods for early detection of cancer, even premalignant lesions, may provide more favorable outcomes. Pancreatic intraepithelial neoplasias (PanINs) have been identified as premalignant precursor lesions to pancreatic cancer. However, conventional imaging methods used for screening high-risk populations do not have the sensitivity to detect PanINs. Here, we have employed hyperpolarized metabolic imaging in vivo and nuclear magnetic resonance ((1)H-NMR) metabolomics ex vivo to identify and understand metabolic changes, towards enabling detection of early PanINs and progression to advanced PanINs lesions that precede pancreatic cancer formation. Progression of disease from tissue containing predominantly low-grade PanINs to tissue with high-grade PanINs showed a decreasing alanine/lactate ratio from high-resolution NMR metabolomics ex vivo. Hyperpolarized magnetic resonance spectroscopy (HP-MRS) allows over 10,000-fold sensitivity enhancement relative to conventional magnetic resonance. Real-time HP-MRS was employed to measure non-invasively changes of alanine and lactate metabolites with disease progression and in control mice in vivo, following injection of hyperpolarized [1-(13)C] pyruvate. The alanine-to-lactate signal intensity ratio was found to decrease as the disease progressed from low-grade PanINs to high-grade PanINs. The biochemical changes of alanine transaminase (ALT) and lactate dehydrogenase (LDH) enzyme activity were assessed. These results demonstrate that there are significant alterations of ALT and LDH activities during the transformation from early to advanced PanINs lesions. Furthermore, we demonstrate that real-time conversion kinetic rate constants (k(PA) and k(PL)) can be used as metabolic imaging biomarkers of pancreatic premalignant lesions. Findings from this emerging HP-MRS technique can be translated to the clinic for detection of pancreatic premalignant lesion in high-risk populations. MDPI 2020-05-25 /pmc/articles/PMC7279395/ /pubmed/32466260 http://dx.doi.org/10.3390/ijms21103722 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dutta, Prasanta
Castro Pando, Susana
Mascaro, Marilina
Riquelme, Erick
Zoltan, Michelle
Zacharias, Niki M.
Gammon, Seth T.
Piwnica-Worms, David
Pagel, Mark D.
Sen, Subrata
Maitra, Anirban
Shams, Shayan
McAllister, Florencia
Bhattacharya, Pratip K.
Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy
title Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy
title_full Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy
title_fullStr Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy
title_full_unstemmed Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy
title_short Early Detection of Pancreatic Intraepithelial Neoplasias (PanINs) in Transgenic Mouse Model by Hyperpolarized (13)C Metabolic Magnetic Resonance Spectroscopy
title_sort early detection of pancreatic intraepithelial neoplasias (panins) in transgenic mouse model by hyperpolarized (13)c metabolic magnetic resonance spectroscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279395/
https://www.ncbi.nlm.nih.gov/pubmed/32466260
http://dx.doi.org/10.3390/ijms21103722
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