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Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes

Pituitary adenomas (PAs) are benign growths arising from epithelial cells in the adenohypophysis of the pituitary gland. To date, there has been no detailed metabolic characterization of PAs of various subtypes. In this study, we report nuclear magnetic resonance (NMR) based metabolomic analysis of...

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Autores principales: Ijare, Omkar B., Baskin, David S., Pichumani, Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395808/
https://www.ncbi.nlm.nih.gov/pubmed/30816132
http://dx.doi.org/10.1038/s41598-019-38542-6
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author Ijare, Omkar B.
Baskin, David S.
Pichumani, Kumar
author_facet Ijare, Omkar B.
Baskin, David S.
Pichumani, Kumar
author_sort Ijare, Omkar B.
collection PubMed
description Pituitary adenomas (PAs) are benign growths arising from epithelial cells in the adenohypophysis of the pituitary gland. To date, there has been no detailed metabolic characterization of PAs of various subtypes. In this study, we report nuclear magnetic resonance (NMR) based metabolomic analysis of surgically resected tumors from forty five pituitary tumor patients [gonadotropic (LH/FSH-secreting) = 17; prolactinomas (PRL-secreting) = 11, Cushing’s disease (ACTH-secreting) = 4, non-functional = 5, and mixed = 8] who underwent transsphenoidal selective adenomectomy. Compared to LH/FSH-secreting tumors, PRL-secreting tumors showed statistically significant decrease in the levels of N-acetylaspartate (NAA), myo-inositol (mI), scyllo-inositol (sI), glycine, taurine, phosphoethanolamine (PE) and increase in the levels of glutamine. When compared with LH/FSH-secreting tumors, ACTH-secreting tumors showed statistically significant decrease in the levels of sI, glycine, PE and increase in the levels of aspartate. Although lipid extracts of PAs showed the presence of many common lipid molecules, only glycerophosphoethanolamine (GPE) showed statistically significant decrease in PRL, ACTH and non-functional subtypes when compared to LH/FSH-secreting tumors. Changes observed in these metabolite concentrations among various subtypes of PAs reflect metabolic heterogeneity in these tumors and may pave the way towards the development of metabolic markers to distinguish various immunohistochemical subtypes of PAs.
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spelling pubmed-63958082019-03-05 Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes Ijare, Omkar B. Baskin, David S. Pichumani, Kumar Sci Rep Article Pituitary adenomas (PAs) are benign growths arising from epithelial cells in the adenohypophysis of the pituitary gland. To date, there has been no detailed metabolic characterization of PAs of various subtypes. In this study, we report nuclear magnetic resonance (NMR) based metabolomic analysis of surgically resected tumors from forty five pituitary tumor patients [gonadotropic (LH/FSH-secreting) = 17; prolactinomas (PRL-secreting) = 11, Cushing’s disease (ACTH-secreting) = 4, non-functional = 5, and mixed = 8] who underwent transsphenoidal selective adenomectomy. Compared to LH/FSH-secreting tumors, PRL-secreting tumors showed statistically significant decrease in the levels of N-acetylaspartate (NAA), myo-inositol (mI), scyllo-inositol (sI), glycine, taurine, phosphoethanolamine (PE) and increase in the levels of glutamine. When compared with LH/FSH-secreting tumors, ACTH-secreting tumors showed statistically significant decrease in the levels of sI, glycine, PE and increase in the levels of aspartate. Although lipid extracts of PAs showed the presence of many common lipid molecules, only glycerophosphoethanolamine (GPE) showed statistically significant decrease in PRL, ACTH and non-functional subtypes when compared to LH/FSH-secreting tumors. Changes observed in these metabolite concentrations among various subtypes of PAs reflect metabolic heterogeneity in these tumors and may pave the way towards the development of metabolic markers to distinguish various immunohistochemical subtypes of PAs. Nature Publishing Group UK 2019-02-28 /pmc/articles/PMC6395808/ /pubmed/30816132 http://dx.doi.org/10.1038/s41598-019-38542-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ijare, Omkar B.
Baskin, David S.
Pichumani, Kumar
Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes
title Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes
title_full Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes
title_fullStr Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes
title_full_unstemmed Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes
title_short Ex Vivo(1)H NMR study of pituitary adenomas to differentiate various immunohistochemical subtypes
title_sort ex vivo(1)h nmr study of pituitary adenomas to differentiate various immunohistochemical subtypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395808/
https://www.ncbi.nlm.nih.gov/pubmed/30816132
http://dx.doi.org/10.1038/s41598-019-38542-6
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