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Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions

Thyroid cancer is the most common endocrine malignancy. However, more than 90% of thyroid nodules are benign. It remains unclear whether thyroid carcinoma arises from preexisting benign nodules. Metabolomics can provide valuable and comprehensive information about low molecular weight compounds pres...

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Autores principales: Deja, Stanisław, Dawiskiba, Tomasz, Balcerzak, Waldemar, Orczyk-Pawiłowicz, Magdalena, Głód, Mateusz, Pawełka, Dorota, Młynarz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871661/
https://www.ncbi.nlm.nih.gov/pubmed/24376829
http://dx.doi.org/10.1371/journal.pone.0084637
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author Deja, Stanisław
Dawiskiba, Tomasz
Balcerzak, Waldemar
Orczyk-Pawiłowicz, Magdalena
Głód, Mateusz
Pawełka, Dorota
Młynarz, Piotr
author_facet Deja, Stanisław
Dawiskiba, Tomasz
Balcerzak, Waldemar
Orczyk-Pawiłowicz, Magdalena
Głód, Mateusz
Pawełka, Dorota
Młynarz, Piotr
author_sort Deja, Stanisław
collection PubMed
description Thyroid cancer is the most common endocrine malignancy. However, more than 90% of thyroid nodules are benign. It remains unclear whether thyroid carcinoma arises from preexisting benign nodules. Metabolomics can provide valuable and comprehensive information about low molecular weight compounds present in living systems and further our understanding of the biology regulating pathological processes. Herein, we applied (1)H NMR-based metabolic profiling to identify the metabolites present in aqueous tissue extracts of healthy thyroid tissue (H), non-neoplastic nodules (NN), follicular adenomas (FA) and malignant thyroid cancer (TC) as an alternative way of investigating cancer lesions. Multivariate statistical methods provided clear discrimination not only between healthy thyroid tissue and pathological thyroid tissue but also between different types of thyroid lesions. Potential biomarkers common to all thyroid lesions were identified, namely, alanine, methionine, acetone, glutamate, glycine, lactate, tyrosine, phenylalanine and hypoxanthine. Metabolic changes in thyroid cancer were mainly related to osmotic regulators (taurine and scyllo- and myo-inositol), citrate, and amino acids supplying the TCA cycle. Thyroid follicular adenomas were found to display metabolic features of benign non-neoplastic nodules and simultaneously displayed a partial metabolic profile associated with malignancy. This finding allows the discrimination of follicular adenomas from benign non-neoplastic nodules and thyroid cancer with similar accuracy. Moreover, the presented data indicate that follicular adenoma could be an individual stage of thyroid cancer development.
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spelling pubmed-38716612013-12-27 Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions Deja, Stanisław Dawiskiba, Tomasz Balcerzak, Waldemar Orczyk-Pawiłowicz, Magdalena Głód, Mateusz Pawełka, Dorota Młynarz, Piotr PLoS One Research Article Thyroid cancer is the most common endocrine malignancy. However, more than 90% of thyroid nodules are benign. It remains unclear whether thyroid carcinoma arises from preexisting benign nodules. Metabolomics can provide valuable and comprehensive information about low molecular weight compounds present in living systems and further our understanding of the biology regulating pathological processes. Herein, we applied (1)H NMR-based metabolic profiling to identify the metabolites present in aqueous tissue extracts of healthy thyroid tissue (H), non-neoplastic nodules (NN), follicular adenomas (FA) and malignant thyroid cancer (TC) as an alternative way of investigating cancer lesions. Multivariate statistical methods provided clear discrimination not only between healthy thyroid tissue and pathological thyroid tissue but also between different types of thyroid lesions. Potential biomarkers common to all thyroid lesions were identified, namely, alanine, methionine, acetone, glutamate, glycine, lactate, tyrosine, phenylalanine and hypoxanthine. Metabolic changes in thyroid cancer were mainly related to osmotic regulators (taurine and scyllo- and myo-inositol), citrate, and amino acids supplying the TCA cycle. Thyroid follicular adenomas were found to display metabolic features of benign non-neoplastic nodules and simultaneously displayed a partial metabolic profile associated with malignancy. This finding allows the discrimination of follicular adenomas from benign non-neoplastic nodules and thyroid cancer with similar accuracy. Moreover, the presented data indicate that follicular adenoma could be an individual stage of thyroid cancer development. Public Library of Science 2013-12-23 /pmc/articles/PMC3871661/ /pubmed/24376829 http://dx.doi.org/10.1371/journal.pone.0084637 Text en © 2013 Deja et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Deja, Stanisław
Dawiskiba, Tomasz
Balcerzak, Waldemar
Orczyk-Pawiłowicz, Magdalena
Głód, Mateusz
Pawełka, Dorota
Młynarz, Piotr
Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions
title Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions
title_full Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions
title_fullStr Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions
title_full_unstemmed Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions
title_short Follicular Adenomas Exhibit a Unique Metabolic Profile. (1)H NMR Studies of Thyroid Lesions
title_sort follicular adenomas exhibit a unique metabolic profile. (1)h nmr studies of thyroid lesions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871661/
https://www.ncbi.nlm.nih.gov/pubmed/24376829
http://dx.doi.org/10.1371/journal.pone.0084637
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