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Zongjing Zhang Division of Endocrinology, Department of Endocrinology and Metabolism, Diabetes, and Metabolism, Laboratory for Cellular and Molecular Thyroid Research, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA
Division of Endocrinology, Department of Endocrinology and Metabolism, Diabetes, and Metabolism, Laboratory for Cellular and Molecular Thyroid Research, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Dingxie Liu Division of Endocrinology, Department of Endocrinology and Metabolism, Diabetes, and Metabolism, Laboratory for Cellular and Molecular Thyroid Research, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Avaniyapuram Kannan Murugan Division of Endocrinology, Department of Endocrinology and Metabolism, Diabetes, and Metabolism, Laboratory for Cellular and Molecular Thyroid Research, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Zhimin Liu Division of Endocrinology, Department of Endocrinology and Metabolism, Diabetes, and Metabolism, Laboratory for Cellular and Molecular Thyroid Research, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Mingzhao Xing Division of Endocrinology, Department of Endocrinology and Metabolism, Diabetes, and Metabolism, Laboratory for Cellular and Molecular Thyroid Research, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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TATA box, TTF1,AP1, AP2, Sp1, and cAMP response element-binding protein (CREB) binding sites in human NIS promoter ( Ryu et al . 1998 ). The regions P1 (−297/−107), P2 (−477/−277), and P3 (−678/−452) harbor many of these transcription factor

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-13-0399
Volume/Issue:
Volume 21: Issue 2
Open access
Su Jung Oh
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Holger H H Erb
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Alfred Hobisch Division of Experimental Urology, Department of Urology, Department of Urology, Innsbruck Medical University, Anichstrasse 35, A-6020 Innsbruck, Austria

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Frédéric R Santer
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Zoran Culig
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expression of cofactors which potentiate agonistic effects of hydroxyflutamide, such as CREB-binding protein (CBP) or gelsolin ( Culig et al . 2005 ). For this reason, a novel AR antagonist, such as MDV3100, which acts by a different mechanism in comparison

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-11-0298
Volume/Issue:
Volume 19: Issue 3
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Martina Gruber Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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Lavinia Ferrone Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria
Department of Biomedical, Experimental and Clinical Sciences, University of Florence, Florence, Italy

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Martin Puhr Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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Frédéric R Santer Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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Tobias Furlan Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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Iris E Eder Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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Natalie Sampson Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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Georg Schäfer Department of Pathology, Neuropathology, and Molecular Pathology, Medical University of Innsbruck, Innsbruck, Austria

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Florian Handle Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria
Molecular Endocrinology Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium

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Zoran Culig Division of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria

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(CREB binding protein) that show elevated expression in advanced PCa and have oncogenic potential ( Debes et al. 2003 , Comuzzi et al. 2004 ). While these coactivators show high levels of homology, they play distinctive roles in PCa and other

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-19-0488
Volume/Issue:
Volume 27: Issue 3
Open access
Maria Angela De Stefano Department of Public Health, University of Naples “Federico II”, Naples, Italy

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Tommaso Porcelli Department of Public Health, University of Naples “Federico II”, Naples, Italy

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Martin Schlumberger Department of Endocrine Oncology, Gustave Roussy and University Paris-Saclay, Villejuif, France

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Domenico Salvatore Department of Public Health, University of Naples “Federico II”, Naples, Italy
CEINGE Biotecnologie Avanzate Scarl, Naples, Italy

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',5'-cyclic adenosine monophosphate response element binding protein (CREB) is functionally reduced in human toxic thyroid adenomas . Endocrinology 141 722 – 730 . ( https://doi.org/10.1210/endo.141.2.7331 ) 10650954 Callebaut I Curcio-Morelli C Mornon

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-23-0015
Volume/Issue:
Volume 30: Issue 5
Open access
N Burrows School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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J Resch School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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R L Cowen School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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R von Wasielewski School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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C Hoang-Vu School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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C M West School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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K J Williams School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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G Brabant School of Pharmacy and Pharmaceutical Sciences, Department of Endocrinology, Department of Pathology, Experimental and Surgical Oncology, Academic Department of Radiation Oncology, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK

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degraded in the proteasome via the ubiquitination pathway ( Pouyssegur et al . 2006 ). In hypoxia, HIF-1α is stabilized, translocates to the nucleus and, following heterodimerization with HIF-1β and cofactors like CREB-binding protein (CBP)/p300

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-08-0251
Volume/Issue:
Volume 17: Issue 1
Open access
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Paul Benjamin Loughrey Patrick G Johnston Centre for Cancer Research, Queen’s University, Belfast, UK
Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK

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Federico Roncaroli Geoffrey Jefferson Brain Research Centre, Division of Neuroscience and Experimental Psychology, School of Medicine, Manchester University, Manchester, UK

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Estelle Healy Department of Cellular Pathology, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK

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Philip Weir Department of Neurosurgery, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK

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Madhu Basetti Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK

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Ruth T Casey Department of Endocrinology, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK

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Steven J Hunter Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK

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Márta Korbonits Centre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK

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, and a recent study has established a link between HIF-1α excess and protein kinase A, CREB and downstream excess growth hormone secretion via repression of PRKAR2B transcription ( Lucia et al. 2020 ). SDHx variants SDHB , SDHA and SDHC

Article Type:
Review Article
Collections:
Advances and Future Directions in Pheochromocytoma and Paraganglioma
DOI:
https://doi.org/10.1530/ERC-22-0157
Volume/Issue:
Volume 29: Issue 10
Open access
Jesús Morillo-Bernal Instituto de Investigaciones Biomédicas ‘Alberto Sols’, Consejo Superior Investigaciones Científicas, and Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain

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Lara P Fernández Instituto de Investigaciones Biomédicas ‘Alberto Sols’, Consejo Superior Investigaciones Científicas, and Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain
Molecular Oncology Group, IMDEA Food Institute, CEI UAM-CSIC, Madrid, Spain

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Pilar Santisteban Instituto de Investigaciones Biomédicas ‘Alberto Sols’, Consejo Superior Investigaciones Científicas, and Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain
Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Instituto de Salud Carlos III (ISCIII), Madrid, Spain

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-Marquez A Fernandez-Mendez C Recacha P Santisteban P 2019 Regulation of Foxe1 by TSH and TGFbeta depends on the interplay between thyroid-specific, CREB and SMAD transcription factors . Thyroid 714 – 725 . ( https://doi.org/10.1089/thy.2018

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-19-0156
Volume/Issue:
Volume 27: Issue 3
Open access
Simon Linder Division of Oncogenomics, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands

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Henk G van der Poel Division of Urology, The Netherlands Cancer Institute, Amsterdam, The Netherlands

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Andries M Bergman Division of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
Division of Oncogenomics, The Netherlands Cancer Institute, Amsterdam, The Netherlands

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Wilbert Zwart Division of Oncogenomics, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands
Laboratory of Chemical Biology and Institute for Complex Molecular Systems, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands

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Stefan Prekovic Division of Oncogenomics, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands

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that target a subset of AR coregulators and thus serve as a proof of principle. Recently, several inhibitors of the histone acetyltransferases E1A-binding protein (p300) and cAMP response element-binding protein (CREB)-binding protein (CBP) have been

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-18-0289
Volume/Issue:
Volume 26: Issue 1
Open access