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GATA transcription factors in testicular adrenal rest tumours
Testicular adrenal rest tumours (TARTs) are benign adrenal-like testicular tumours that frequently occur in male patients with congenital adrenal hyperplasia. Recently, GATA transcription factors have been linked to the development of TARTs in mice. The aim of our study was to determine GATA express...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682415/ https://www.ncbi.nlm.nih.gov/pubmed/29038332 http://dx.doi.org/10.1530/EC-17-0215 |
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author | Engels, Manon Span, Paul N Mitchell, Rod T Heuvel, Joop J T M Marijnissen-van Zanten, Monica A van Herwaarden, Antonius E Hulsbergen-van de Kaa, Christina A Oosterwijk, Egbert Stikkelbroeck, Nike M Smith, Lee B Sweep, Fred C G J Claahsen-van der Grinten, Hedi L |
author_facet | Engels, Manon Span, Paul N Mitchell, Rod T Heuvel, Joop J T M Marijnissen-van Zanten, Monica A van Herwaarden, Antonius E Hulsbergen-van de Kaa, Christina A Oosterwijk, Egbert Stikkelbroeck, Nike M Smith, Lee B Sweep, Fred C G J Claahsen-van der Grinten, Hedi L |
author_sort | Engels, Manon |
collection | PubMed |
description | Testicular adrenal rest tumours (TARTs) are benign adrenal-like testicular tumours that frequently occur in male patients with congenital adrenal hyperplasia. Recently, GATA transcription factors have been linked to the development of TARTs in mice. The aim of our study was to determine GATA expression in human TARTs and other steroidogenic tissues. We determined GATA expression in TARTs (n = 16), Leydig cell tumours (LCTs; n = 7), adrenal (foetal (n = 6) + adult (n = 10)) and testis (foetal (n = 13) + adult (n = 8)). We found testis-like GATA4, and adrenal-like GATA3 and GATA6 gene expressions by qPCR in human TARTs, indicating mixed testicular and adrenal characteristics of TARTs. Currently, no marker is available to discriminate TARTs from LCTs, leading to misdiagnosis and incorrect treatment. GATA3 and GATA6 mRNAs exhibited excellent discriminative power (area under the curve of 0.908 and 0.816, respectively), while immunohistochemistry did not. GATA genes contain several CREB-binding sites and incubation with 0.1 mM dibutyryl cAMP for 4 h stimulated GATA3, GATA4 and GATA6 expressions in a human foetal testis cell line (hs181.tes). Incubation of adrenocortical cells (H295RA) with ACTH, however, did not induce GATA expression in vitro. Although ACTH did not dysregulate GATA expression in the only human ACTH-sensitive in vitro model available, our results do suggest that aberrant expression of GATA transcription factors in human TARTs might be involved in TART formation. |
format | Online Article Text |
id | pubmed-5682415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56824152017-11-16 GATA transcription factors in testicular adrenal rest tumours Engels, Manon Span, Paul N Mitchell, Rod T Heuvel, Joop J T M Marijnissen-van Zanten, Monica A van Herwaarden, Antonius E Hulsbergen-van de Kaa, Christina A Oosterwijk, Egbert Stikkelbroeck, Nike M Smith, Lee B Sweep, Fred C G J Claahsen-van der Grinten, Hedi L Endocr Connect Research Testicular adrenal rest tumours (TARTs) are benign adrenal-like testicular tumours that frequently occur in male patients with congenital adrenal hyperplasia. Recently, GATA transcription factors have been linked to the development of TARTs in mice. The aim of our study was to determine GATA expression in human TARTs and other steroidogenic tissues. We determined GATA expression in TARTs (n = 16), Leydig cell tumours (LCTs; n = 7), adrenal (foetal (n = 6) + adult (n = 10)) and testis (foetal (n = 13) + adult (n = 8)). We found testis-like GATA4, and adrenal-like GATA3 and GATA6 gene expressions by qPCR in human TARTs, indicating mixed testicular and adrenal characteristics of TARTs. Currently, no marker is available to discriminate TARTs from LCTs, leading to misdiagnosis and incorrect treatment. GATA3 and GATA6 mRNAs exhibited excellent discriminative power (area under the curve of 0.908 and 0.816, respectively), while immunohistochemistry did not. GATA genes contain several CREB-binding sites and incubation with 0.1 mM dibutyryl cAMP for 4 h stimulated GATA3, GATA4 and GATA6 expressions in a human foetal testis cell line (hs181.tes). Incubation of adrenocortical cells (H295RA) with ACTH, however, did not induce GATA expression in vitro. Although ACTH did not dysregulate GATA expression in the only human ACTH-sensitive in vitro model available, our results do suggest that aberrant expression of GATA transcription factors in human TARTs might be involved in TART formation. Bioscientifica Ltd 2017-10-16 /pmc/articles/PMC5682415/ /pubmed/29038332 http://dx.doi.org/10.1530/EC-17-0215 Text en © 2017 The authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Engels, Manon Span, Paul N Mitchell, Rod T Heuvel, Joop J T M Marijnissen-van Zanten, Monica A van Herwaarden, Antonius E Hulsbergen-van de Kaa, Christina A Oosterwijk, Egbert Stikkelbroeck, Nike M Smith, Lee B Sweep, Fred C G J Claahsen-van der Grinten, Hedi L GATA transcription factors in testicular adrenal rest tumours |
title | GATA transcription factors in testicular adrenal rest tumours |
title_full | GATA transcription factors in testicular adrenal rest tumours |
title_fullStr | GATA transcription factors in testicular adrenal rest tumours |
title_full_unstemmed | GATA transcription factors in testicular adrenal rest tumours |
title_short | GATA transcription factors in testicular adrenal rest tumours |
title_sort | gata transcription factors in testicular adrenal rest tumours |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682415/ https://www.ncbi.nlm.nih.gov/pubmed/29038332 http://dx.doi.org/10.1530/EC-17-0215 |
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