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Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma

BACKGROUND: Human infection with Opisthorchis viverrini, a carcinogenic liver fluke inhabiting the biliary tree, is endemic in Southeast Asia. Chronic infection is associated with a fatal complication, cholangiocarcinoma (CCA), a late-presenting and aggressive malignancy. Currently, annual mortality...

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Autores principales: Alsaleh, Munirah, Sithithaworn, Paiboon, Khuntikeo, Narong, Loilome, Watcharin, Yongvanit, Puangrat, Chamadol, Nittaya, Hughes, Thomas, O'Connor, Thomas, Andrews, Ross H., Holmes, Elaine, Taylor-Robinson, Simon D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926188/
https://www.ncbi.nlm.nih.gov/pubmed/31889746
http://dx.doi.org/10.1016/j.jceh.2019.06.005
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author Alsaleh, Munirah
Sithithaworn, Paiboon
Khuntikeo, Narong
Loilome, Watcharin
Yongvanit, Puangrat
Chamadol, Nittaya
Hughes, Thomas
O'Connor, Thomas
Andrews, Ross H.
Holmes, Elaine
Taylor-Robinson, Simon D.
author_facet Alsaleh, Munirah
Sithithaworn, Paiboon
Khuntikeo, Narong
Loilome, Watcharin
Yongvanit, Puangrat
Chamadol, Nittaya
Hughes, Thomas
O'Connor, Thomas
Andrews, Ross H.
Holmes, Elaine
Taylor-Robinson, Simon D.
author_sort Alsaleh, Munirah
collection PubMed
description BACKGROUND: Human infection with Opisthorchis viverrini, a carcinogenic liver fluke inhabiting the biliary tree, is endemic in Southeast Asia. Chronic infection is associated with a fatal complication, cholangiocarcinoma (CCA), a late-presenting and aggressive malignancy. Currently, annual mortality rates from CCA mirror trends in incidence, due in part to limited availability of efficient prognostic and early diagnostic biomarkers. With ability to detect thousands of urinary metabolites using metabonomics, the urine metabolome holds great potential in providing an insight into system-level alterations in carcinogenesis and in identifying metabolic markers altered in response to disturbed homoeostasis. METHODS: Global molecular profiling using reversed-phase ultraperformance liquid chromatography mass spectrometry was utilised to acquire the urinary spectral profile of 137 Thai subjects (48 at high risk of infection, 41 with O. viverrini infection, 34 periportal fibrosis and 14 CCA) from Khon Kaen, Thailand. RESULTS: Multivariate statistical analysis identified perturbation in several molecular classes related to purine metabolism and lipid metabolism in the CCA urine metabolome. These markers mainly reflect changes in energy metabolism to support proliferation (increased fatty acid oxidation and purine recycling), DNA methylation and hepatic injury. CONCLUSIONS: Several metabolites of biological interest were discovered from this proof-of-principle dataset. Augmenting these findings is essential to accelerate the development of urinary metabolic markers in CCA.
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spelling pubmed-69261882020-11-01 Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma Alsaleh, Munirah Sithithaworn, Paiboon Khuntikeo, Narong Loilome, Watcharin Yongvanit, Puangrat Chamadol, Nittaya Hughes, Thomas O'Connor, Thomas Andrews, Ross H. Holmes, Elaine Taylor-Robinson, Simon D. J Clin Exp Hepatol Original Article BACKGROUND: Human infection with Opisthorchis viverrini, a carcinogenic liver fluke inhabiting the biliary tree, is endemic in Southeast Asia. Chronic infection is associated with a fatal complication, cholangiocarcinoma (CCA), a late-presenting and aggressive malignancy. Currently, annual mortality rates from CCA mirror trends in incidence, due in part to limited availability of efficient prognostic and early diagnostic biomarkers. With ability to detect thousands of urinary metabolites using metabonomics, the urine metabolome holds great potential in providing an insight into system-level alterations in carcinogenesis and in identifying metabolic markers altered in response to disturbed homoeostasis. METHODS: Global molecular profiling using reversed-phase ultraperformance liquid chromatography mass spectrometry was utilised to acquire the urinary spectral profile of 137 Thai subjects (48 at high risk of infection, 41 with O. viverrini infection, 34 periportal fibrosis and 14 CCA) from Khon Kaen, Thailand. RESULTS: Multivariate statistical analysis identified perturbation in several molecular classes related to purine metabolism and lipid metabolism in the CCA urine metabolome. These markers mainly reflect changes in energy metabolism to support proliferation (increased fatty acid oxidation and purine recycling), DNA methylation and hepatic injury. CONCLUSIONS: Several metabolites of biological interest were discovered from this proof-of-principle dataset. Augmenting these findings is essential to accelerate the development of urinary metabolic markers in CCA. Elsevier 2019 2019-07-31 /pmc/articles/PMC6926188/ /pubmed/31889746 http://dx.doi.org/10.1016/j.jceh.2019.06.005 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Alsaleh, Munirah
Sithithaworn, Paiboon
Khuntikeo, Narong
Loilome, Watcharin
Yongvanit, Puangrat
Chamadol, Nittaya
Hughes, Thomas
O'Connor, Thomas
Andrews, Ross H.
Holmes, Elaine
Taylor-Robinson, Simon D.
Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma
title Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma
title_full Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma
title_fullStr Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma
title_full_unstemmed Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma
title_short Characterisation of the Urinary Metabolic Profile of Liver Fluke-Associated Cholangiocarcinoma
title_sort characterisation of the urinary metabolic profile of liver fluke-associated cholangiocarcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926188/
https://www.ncbi.nlm.nih.gov/pubmed/31889746
http://dx.doi.org/10.1016/j.jceh.2019.06.005
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