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Department of Endocrinology, APHP, Cochin Hospital, Paris, France
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-Rabin M Assie G Groussin L Fierrard H Perlemoine K Martinez A Bertherat J 2009 Inactivation of the Carney complex gene 1 (protein kinase A regulatory subunit 1A) inhibits SMAD3 expression and TGF beta-stimulated apoptosis in adrenocortical
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Medizinische Klinik und Poliklinik III, University Hospital Carl Gustav Carus Dresden, Dresden, Germany
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Department of Endocrinology and National Reference Center for Rare Adrenal Disorders, Hôpital Cochin, Assistance Publique Hôpitaux de Paris, Paris, France
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(protein kinase A regulatory subunit 1A) inhibits SMAD3 expression and TGF beta-stimulated apoptosis in adrenocortical cells . Cancer Research 69 7278 – 7284 . ( https://doi.org/10.1158/0008-5472.CAN-09-1601 ) Sablina AA Budanov AV Ilyinskaya GV
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Department of Clinical Therapeutics, Alexandra Hospital Athens University School of Medicine, Endocrine Unit, Athens, Greece
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. Azouzi and Schlumberger focused on the role of reactive oxygen species (ROS)-generating NADPH oxidase (NOX4) which is increased in PTC ( Azouzi et al. 2017 ). Their study revealed that BRAF- V600E upregulates NOX4 expression via the TGFB/SMAD3 signaling
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treated with anti-miR-19 through Notch pathway inhibition and there was restoration of responsiveness to TGFβ signaling ( Fuziwara & Kimura 2014 ). Notch and TGFβ/Smad3 pathways are involved in the interaction between cancer cells and cancer
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) and the promotion of cell migration, invasiveness and EMT ( Knauf et al. 2011 ). Recently, we showed that NOX4 is upregulated by BRAF V600E via a TGF-β-Smad3-dependent pathway in thyroid cancer cells and that NOX4-dependent ROS generation has a
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order to overcome resistance to endocrine therapy ( Miller et al. 2010 ). Menin, encoded by the MEN1 gene, is a multifaceted cofactor, interacting physically or functionally with numerous transcription and epigenetic factors, including Smad3, JunD
Department of Pharmacy, Pulmonary Hospital of Wuhan, Wuhan, China
Faculty of Pharmacy, Hubei University of Chinese Medicine, Wuhan, China
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. ( https://doi.org/10.1038/15275 ) Hu B Mao Z Du Q Jiang X Wang Z Xiao Z Zhu D Wang X Zhu Y Wang H 2019 miR-93-5p targets Smad7 to regulate the transforming growth factor-beta1/Smad3 pathway and mediate fibrosis in drug
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. ( doi:10.1074/jbc.M109889200 ) Tone Y Furuuchi K Kojima Y Tykocinski ML Greene MI Tone M 2008 Smad3 and NFAT cooperate to induce Foxp3 expression through its enhancer . Nature Immunology 9 194 – 202 . ( doi:10.1038/ni
Department of Physiology and Cell Biology, Molecular, Genomic Medicine, Laboratory of Human Cancer Genetics, Center for Biostatistics, Cellular and Developmental Biology Graduate Program, The Ohio State University, 1645 Neil Avenue, 304 Hamilton Hall, Columbus, Ohio 43210, USA
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Department of Physiology and Cell Biology, Molecular, Genomic Medicine, Laboratory of Human Cancer Genetics, Center for Biostatistics, Cellular and Developmental Biology Graduate Program, The Ohio State University, 1645 Neil Avenue, 304 Hamilton Hall, Columbus, Ohio 43210, USA
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Department of Physiology and Cell Biology, Molecular, Genomic Medicine, Laboratory of Human Cancer Genetics, Center for Biostatistics, Cellular and Developmental Biology Graduate Program, The Ohio State University, 1645 Neil Avenue, 304 Hamilton Hall, Columbus, Ohio 43210, USA
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Department of Physiology and Cell Biology, Molecular, Genomic Medicine, Laboratory of Human Cancer Genetics, Center for Biostatistics, Cellular and Developmental Biology Graduate Program, The Ohio State University, 1645 Neil Avenue, 304 Hamilton Hall, Columbus, Ohio 43210, USA
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and Smad3 is involved in transforming growth factor-β repression of the sodium/iodide symporter gene . Journal of Biological Chemistry 279 3439 – 3446 . ( doi:10.1074/jbc.M307138200 ). Dima M Miller KA Antico-Arciuch VG Di Cristofano A
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govern metastatic colonization . Nature 481 85 – 89 . ( doi:10.1038/nature10694 ). Malek D Gust R Kleuser B 2006 17-β-Estradiol inhibits transforming-growth-factor-β-induced MCF-7 cell migration by Smad3-repression . European Journal of