Cargando…

New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A

Cushing’s disease (CD) is an endocrine disorder originated by a corticotroph tumor. It is linked with high mortality and morbidity due to chronic hypercortisolism. Treatment goals are to control cortisol excess and achieve long-term remission, therefore, reducing both complications and patient’s mor...

Descripción completa

Detalles Bibliográficos
Autores principales: Fuertes, Mariana, Tkatch, Julieta, Rosmino, Josefina, Nieto, Leandro, Guitelman, Mirtha Adriana, Arzt, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976796/
https://www.ncbi.nlm.nih.gov/pubmed/29881371
http://dx.doi.org/10.3389/fendo.2018.00262
_version_ 1783327235277586432
author Fuertes, Mariana
Tkatch, Julieta
Rosmino, Josefina
Nieto, Leandro
Guitelman, Mirtha Adriana
Arzt, Eduardo
author_facet Fuertes, Mariana
Tkatch, Julieta
Rosmino, Josefina
Nieto, Leandro
Guitelman, Mirtha Adriana
Arzt, Eduardo
author_sort Fuertes, Mariana
collection PubMed
description Cushing’s disease (CD) is an endocrine disorder originated by a corticotroph tumor. It is linked with high mortality and morbidity due to chronic hypercortisolism. Treatment goals are to control cortisol excess and achieve long-term remission, therefore, reducing both complications and patient’s mortality. First-line of treatment for CD is pituitary’s surgery. However, 30% of patients who undergo surgery experience recurrence in long-term follow-up. Persistent or recurrent CD demands second-line treatments, such as pituitary radiotherapy, adrenal surgery, and/or pharmacological therapy. The latter plays a key role in cortisol excess control. Its targets are inhibition of adrenocorticotropic hormone (ACTH) production, inhibition of adrenal steroidogenesis, or antagonism of cortisol action at its peripheral receptor. Retinoic acid (RA) is a metabolic product of vitamin A (retinol) and has been studied for its antiproliferative effects on corticotroph tumor cells. It has been shown that this drug regulates the expression of pro-opiomelanocortin (POMC), ACTH secretion, and tumor growth in corticotroph tumor mouse cell lines and in the nude mice experimental model, via inhibition of POMC transcription. It has been shown to result in tumor reduction, normalization of cortisol levels and clinical improvement in dogs treated with RA for 6 months. The orphan nuclear receptor COUP-TFI is expressed in normal corticotroph cells, but not in corticotroph tumoral cells, and inhibits RA pathways. A first clinical human study demonstrated clinical and biochemical effectiveness in 5/7 patients treated with RA for a period of up to 12 months. In a recent second clinical trial, 25% of 16 patients achieved eucortisolemia, and all achieved a cortisol reduction after 6- to 12-month treatment. The goal of this review is to discuss in the context of the available and future pharmacological treatments of CD, RA mechanisms of action on corticotroph tumor cells, and future perspectives, focusing on potential clinical implementation.
format Online
Article
Text
id pubmed-5976796
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-59767962018-06-07 New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A Fuertes, Mariana Tkatch, Julieta Rosmino, Josefina Nieto, Leandro Guitelman, Mirtha Adriana Arzt, Eduardo Front Endocrinol (Lausanne) Endocrinology Cushing’s disease (CD) is an endocrine disorder originated by a corticotroph tumor. It is linked with high mortality and morbidity due to chronic hypercortisolism. Treatment goals are to control cortisol excess and achieve long-term remission, therefore, reducing both complications and patient’s mortality. First-line of treatment for CD is pituitary’s surgery. However, 30% of patients who undergo surgery experience recurrence in long-term follow-up. Persistent or recurrent CD demands second-line treatments, such as pituitary radiotherapy, adrenal surgery, and/or pharmacological therapy. The latter plays a key role in cortisol excess control. Its targets are inhibition of adrenocorticotropic hormone (ACTH) production, inhibition of adrenal steroidogenesis, or antagonism of cortisol action at its peripheral receptor. Retinoic acid (RA) is a metabolic product of vitamin A (retinol) and has been studied for its antiproliferative effects on corticotroph tumor cells. It has been shown that this drug regulates the expression of pro-opiomelanocortin (POMC), ACTH secretion, and tumor growth in corticotroph tumor mouse cell lines and in the nude mice experimental model, via inhibition of POMC transcription. It has been shown to result in tumor reduction, normalization of cortisol levels and clinical improvement in dogs treated with RA for 6 months. The orphan nuclear receptor COUP-TFI is expressed in normal corticotroph cells, but not in corticotroph tumoral cells, and inhibits RA pathways. A first clinical human study demonstrated clinical and biochemical effectiveness in 5/7 patients treated with RA for a period of up to 12 months. In a recent second clinical trial, 25% of 16 patients achieved eucortisolemia, and all achieved a cortisol reduction after 6- to 12-month treatment. The goal of this review is to discuss in the context of the available and future pharmacological treatments of CD, RA mechanisms of action on corticotroph tumor cells, and future perspectives, focusing on potential clinical implementation. Frontiers Media S.A. 2018-05-24 /pmc/articles/PMC5976796/ /pubmed/29881371 http://dx.doi.org/10.3389/fendo.2018.00262 Text en Copyright © 2018 Fuertes, Tkatch, Rosmino, Nieto, Guitelman and Arzt. https://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) and the copyright owner 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
Fuertes, Mariana
Tkatch, Julieta
Rosmino, Josefina
Nieto, Leandro
Guitelman, Mirtha Adriana
Arzt, Eduardo
New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A
title New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A
title_full New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A
title_fullStr New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A
title_full_unstemmed New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A
title_short New Insights in Cushing Disease Treatment With Focus on a Derivative of Vitamin A
title_sort new insights in cushing disease treatment with focus on a derivative of vitamin a
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976796/
https://www.ncbi.nlm.nih.gov/pubmed/29881371
http://dx.doi.org/10.3389/fendo.2018.00262
work_keys_str_mv AT fuertesmariana newinsightsincushingdiseasetreatmentwithfocusonaderivativeofvitamina
AT tkatchjulieta newinsightsincushingdiseasetreatmentwithfocusonaderivativeofvitamina
AT rosminojosefina newinsightsincushingdiseasetreatmentwithfocusonaderivativeofvitamina
AT nietoleandro newinsightsincushingdiseasetreatmentwithfocusonaderivativeofvitamina
AT guitelmanmirthaadriana newinsightsincushingdiseasetreatmentwithfocusonaderivativeofvitamina
AT arzteduardo newinsightsincushingdiseasetreatmentwithfocusonaderivativeofvitamina