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Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture

Although TSH has been suggested to be a proliferative agent for thyrocytes, the effect of TSH on human thyroid cells remains controversial. In particular, most of the reported studies relied primarily on changes in DNA synthesis but have not included measurement of the number of cells. We argue that...

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Autores principales: Morgan, Sarah J., Neumann, Susanne, Marcus-Samuels, Bernice, Gershengorn, Marvin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183721/
https://www.ncbi.nlm.nih.gov/pubmed/28082948
http://dx.doi.org/10.3389/fendo.2016.00168
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author Morgan, Sarah J.
Neumann, Susanne
Marcus-Samuels, Bernice
Gershengorn, Marvin C.
author_facet Morgan, Sarah J.
Neumann, Susanne
Marcus-Samuels, Bernice
Gershengorn, Marvin C.
author_sort Morgan, Sarah J.
collection PubMed
description Although TSH has been suggested to be a proliferative agent for thyrocytes, the effect of TSH on human thyroid cells remains controversial. In particular, most of the reported studies relied primarily on changes in DNA synthesis but have not included measurement of the number of cells. We argue that only a direct count of cell number, demonstrating classical exponential expansion, serves as a valid measurement of proliferation. Thus, although some data support TSH as a proliferative agent, most do not provide conclusive evidence. To generate conclusive evidence with regard to a proliferative effect of TSH in human thyrocytes, we performed various experiments using primary cultures of human thyrocytes. In contrast to previous reports, TSH [±insulin-like growth factor 1 (IGF-1)] did not induce proliferation of thyrocytes under a variety of different conditions. However, TSH/IGF-1 cotreatment did upregulate thyroid-specific gene expression including thyroglobulin (TG) and TSHR in a manner consistent with cellular differentiation. Evidence for a proliferative effect of TSH has been used to inform the American Thyroid Association’s guidelines for the management of thyroid cancer patients, which include TSH suppression. While these recommendations are admittedly based on low- to moderate-quality evidence, TSH suppression is still widely used. We present data that question the consensus view that TSH promotes proliferation of human thyrocytes (upon which the American Thyroid Association’s guidelines are based) and suggest that additional studies, including randomized controlled trials, are warranted to address this important clinical question.
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spelling pubmed-51837212017-01-12 Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture Morgan, Sarah J. Neumann, Susanne Marcus-Samuels, Bernice Gershengorn, Marvin C. Front Endocrinol (Lausanne) Endocrinology Although TSH has been suggested to be a proliferative agent for thyrocytes, the effect of TSH on human thyroid cells remains controversial. In particular, most of the reported studies relied primarily on changes in DNA synthesis but have not included measurement of the number of cells. We argue that only a direct count of cell number, demonstrating classical exponential expansion, serves as a valid measurement of proliferation. Thus, although some data support TSH as a proliferative agent, most do not provide conclusive evidence. To generate conclusive evidence with regard to a proliferative effect of TSH in human thyrocytes, we performed various experiments using primary cultures of human thyrocytes. In contrast to previous reports, TSH [±insulin-like growth factor 1 (IGF-1)] did not induce proliferation of thyrocytes under a variety of different conditions. However, TSH/IGF-1 cotreatment did upregulate thyroid-specific gene expression including thyroglobulin (TG) and TSHR in a manner consistent with cellular differentiation. Evidence for a proliferative effect of TSH has been used to inform the American Thyroid Association’s guidelines for the management of thyroid cancer patients, which include TSH suppression. While these recommendations are admittedly based on low- to moderate-quality evidence, TSH suppression is still widely used. We present data that question the consensus view that TSH promotes proliferation of human thyrocytes (upon which the American Thyroid Association’s guidelines are based) and suggest that additional studies, including randomized controlled trials, are warranted to address this important clinical question. Frontiers Media S.A. 2016-12-26 /pmc/articles/PMC5183721/ /pubmed/28082948 http://dx.doi.org/10.3389/fendo.2016.00168 Text en Copyright © 2016 Morgan, Neumann, Marcus-Samuels and Gershengorn. http://creativecommons.org/licenses/by/4.0/ 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
Morgan, Sarah J.
Neumann, Susanne
Marcus-Samuels, Bernice
Gershengorn, Marvin C.
Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture
title Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture
title_full Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture
title_fullStr Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture
title_full_unstemmed Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture
title_short Thyrotropin Stimulates Differentiation Not Proliferation of Normal Human Thyrocytes in Culture
title_sort thyrotropin stimulates differentiation not proliferation of normal human thyrocytes in culture
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183721/
https://www.ncbi.nlm.nih.gov/pubmed/28082948
http://dx.doi.org/10.3389/fendo.2016.00168
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