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Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
The major product secreted by the thyroid is thyroxine (T4), whereas most of the biologically active triiodothyronine (T3) derives from the peripheral conversion of T4 into T3. The deiodinase enzymes are involved in activation and inactivation of thyroid hormones (THs). Type 1 and type 2 deiodinase...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3761349/ https://www.ncbi.nlm.nih.gov/pubmed/24027558 http://dx.doi.org/10.3389/fendo.2013.00115 |
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author | Luongo, Cristina Trivisano, Luigi Alfano, Fausta Salvatore, Domenico |
author_facet | Luongo, Cristina Trivisano, Luigi Alfano, Fausta Salvatore, Domenico |
author_sort | Luongo, Cristina |
collection | PubMed |
description | The major product secreted by the thyroid is thyroxine (T4), whereas most of the biologically active triiodothyronine (T3) derives from the peripheral conversion of T4 into T3. The deiodinase enzymes are involved in activation and inactivation of thyroid hormones (THs). Type 1 and type 2 deiodinase (D1 and D2) convert T4 into T3 whereas D3 degrades T4 and T3 into inactive metabolites and is thus the major physiological TH inactivator. The hypothalamic-pituitary-thyroid axis maintains circulating TH levels constant, while the deiodinases tissue-specifically regulate intracellular thyroid status by controlling TH action in a precise spatio-temporal fashion. Here we review the data related to the recent identification of a paraneoplastic syndrome called “consumptive hypothyroidism,” which exemplifies how deiodinases alter substantially the concentration of TH in blood. This syndrome results from the aberrant uncontrolled expression of D3 that can induce a severe form of hypothyroidism by inactivating T4 and T3 in defined tumor tissue. This rare TH insufficiency generally affects patients in the first years of life, and has distinct features in terms of diagnosis, treatment, and prognosis with respect to other forms of hypothyroidism. |
format | Online Article Text |
id | pubmed-3761349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37613492013-09-11 Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease Luongo, Cristina Trivisano, Luigi Alfano, Fausta Salvatore, Domenico Front Endocrinol (Lausanne) Endocrinology The major product secreted by the thyroid is thyroxine (T4), whereas most of the biologically active triiodothyronine (T3) derives from the peripheral conversion of T4 into T3. The deiodinase enzymes are involved in activation and inactivation of thyroid hormones (THs). Type 1 and type 2 deiodinase (D1 and D2) convert T4 into T3 whereas D3 degrades T4 and T3 into inactive metabolites and is thus the major physiological TH inactivator. The hypothalamic-pituitary-thyroid axis maintains circulating TH levels constant, while the deiodinases tissue-specifically regulate intracellular thyroid status by controlling TH action in a precise spatio-temporal fashion. Here we review the data related to the recent identification of a paraneoplastic syndrome called “consumptive hypothyroidism,” which exemplifies how deiodinases alter substantially the concentration of TH in blood. This syndrome results from the aberrant uncontrolled expression of D3 that can induce a severe form of hypothyroidism by inactivating T4 and T3 in defined tumor tissue. This rare TH insufficiency generally affects patients in the first years of life, and has distinct features in terms of diagnosis, treatment, and prognosis with respect to other forms of hypothyroidism. Frontiers Media S.A. 2013-09-04 /pmc/articles/PMC3761349/ /pubmed/24027558 http://dx.doi.org/10.3389/fendo.2013.00115 Text en Copyright © 2013 Luongo, Trivisano, Alfano and Salvatore. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Luongo, Cristina Trivisano, Luigi Alfano, Fausta Salvatore, Domenico Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease |
title | Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease |
title_full | Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease |
title_fullStr | Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease |
title_full_unstemmed | Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease |
title_short | Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease |
title_sort | type 3 deiodinase and consumptive hypothyroidism: a common mechanism for a rare disease |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3761349/ https://www.ncbi.nlm.nih.gov/pubmed/24027558 http://dx.doi.org/10.3389/fendo.2013.00115 |
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