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Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors

INTRODUCTION: The role of adipokines in neoplasms not related to obesity is unclear. The presence of adiponectin receptors 1 and 2 (AdipoR1 and AdipoR2) as well as the leptin receptor (Ob-R) has been recognized in human adrenal tumors. The authors of the present study were the first to compare the e...

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Autores principales: Babińska, Anna, Pęksa, Rafał, Wiśniewski, Piotr, Sworczak, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764317/
https://www.ncbi.nlm.nih.gov/pubmed/31572471
http://dx.doi.org/10.5114/aoms.2018.76142
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author Babińska, Anna
Pęksa, Rafał
Wiśniewski, Piotr
Sworczak, Krzysztof
author_facet Babińska, Anna
Pęksa, Rafał
Wiśniewski, Piotr
Sworczak, Krzysztof
author_sort Babińska, Anna
collection PubMed
description INTRODUCTION: The role of adipokines in neoplasms not related to obesity is unclear. The presence of adiponectin receptors 1 and 2 (AdipoR1 and AdipoR2) as well as the leptin receptor (Ob-R) has been recognized in human adrenal tumors. The authors of the present study were the first to compare the expression of these receptors in histopathologically distinct adrenal tumors. MATERIAL AND METHODS: The study encompassed tissue specimens of 128 patients with adrenal tumors (28 adrenal cortical adenomas (CA), 35 cortical nodular hyperplasia tumors (CNH), 20 cortical carcinomas (CC), 40 pheochromocytomas (PHEO), 5 malignant pheochromocytomas (PHEOM)) operated on at a single clinical center. The expression of the adiponectin receptors AdipoR1 and AdipoR2 as well as the leptin receptor Ob-R was assessed by immunohistochemistry. The results were correlated with body mass index (BMI) and gender of the patients. RESULTS: AdipoR1 expression was significantly higher in cortical cancers (p < 0.001) and pheochromocytomas (p < 0.001) as compared to benign cortical tumors. AdipoR2 expression was significantly higher in cortical carcinomas as compared to cortical adenomas and hyperplasia tumors (p = 0.01), and also significantly higher in pheochromocytomas in comparison to adrenocortical cancers (p = 0.004). Leptin receptor expression was absent or minimal in half of nodular hyperplasia tumors and adrenal cortex adenomas. This receptor’s expression was significantly higher in adrenocortical cancers (p = 0.038). In pheochromocytomas this receptor was expressed more abundantly than in adrenocortical cancers (p = 0.004). CONCLUSIONS: These novel findings suggest that adiponectin and leptin receptors could play a regulatory role in human adrenal neoplasms.
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spelling pubmed-67643172019-09-30 Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors Babińska, Anna Pęksa, Rafał Wiśniewski, Piotr Sworczak, Krzysztof Arch Med Sci Clinical Research INTRODUCTION: The role of adipokines in neoplasms not related to obesity is unclear. The presence of adiponectin receptors 1 and 2 (AdipoR1 and AdipoR2) as well as the leptin receptor (Ob-R) has been recognized in human adrenal tumors. The authors of the present study were the first to compare the expression of these receptors in histopathologically distinct adrenal tumors. MATERIAL AND METHODS: The study encompassed tissue specimens of 128 patients with adrenal tumors (28 adrenal cortical adenomas (CA), 35 cortical nodular hyperplasia tumors (CNH), 20 cortical carcinomas (CC), 40 pheochromocytomas (PHEO), 5 malignant pheochromocytomas (PHEOM)) operated on at a single clinical center. The expression of the adiponectin receptors AdipoR1 and AdipoR2 as well as the leptin receptor Ob-R was assessed by immunohistochemistry. The results were correlated with body mass index (BMI) and gender of the patients. RESULTS: AdipoR1 expression was significantly higher in cortical cancers (p < 0.001) and pheochromocytomas (p < 0.001) as compared to benign cortical tumors. AdipoR2 expression was significantly higher in cortical carcinomas as compared to cortical adenomas and hyperplasia tumors (p = 0.01), and also significantly higher in pheochromocytomas in comparison to adrenocortical cancers (p = 0.004). Leptin receptor expression was absent or minimal in half of nodular hyperplasia tumors and adrenal cortex adenomas. This receptor’s expression was significantly higher in adrenocortical cancers (p = 0.038). In pheochromocytomas this receptor was expressed more abundantly than in adrenocortical cancers (p = 0.004). CONCLUSIONS: These novel findings suggest that adiponectin and leptin receptors could play a regulatory role in human adrenal neoplasms. Termedia Publishing House 2018-06-01 2019-09 /pmc/articles/PMC6764317/ /pubmed/31572471 http://dx.doi.org/10.5114/aoms.2018.76142 Text en Copyright: © 2018 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Babińska, Anna
Pęksa, Rafał
Wiśniewski, Piotr
Sworczak, Krzysztof
Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
title Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
title_full Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
title_fullStr Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
title_full_unstemmed Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
title_short Expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
title_sort expression of adiponectin receptors 1 and 2 and the leptin receptor in human adrenal tumors
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764317/
https://www.ncbi.nlm.nih.gov/pubmed/31572471
http://dx.doi.org/10.5114/aoms.2018.76142
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