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James F Powers Department of Pathology and Laboratory Medicine, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA

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Brent Cochran Department of Developmental, Molecular and Chemical Biology

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James D Baleja Department of Developmental, Molecular and Chemical Biology

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Hadley D Sikes Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA

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Andrew D Pattison Department of Clinical Pathology, University of Melbourne, Melbourne, Victoria, Australia

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Xue Zhang Department of Developmental, Molecular and Chemical Biology

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Inna Lomakin Department of Pathology and Laboratory Medicine, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA

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Annette Shepard-Barry Department of Pathology and Laboratory Medicine, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA

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Karel Pacak Section on Medical Neuroendocrinology, Eunice Kennedy Shriver Division National Institute of Child Health and Human Development, Bethesda, Maryland, USA

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Sun Jin Moon Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA

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Troy F Langford Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA

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Kassi Taylor Stein Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA

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Richard W Tothill Department of Clinical Pathology, University of Melbourne, Melbourne, Victoria, Australia
Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

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Yingbin Ouyang Cyagen US Inc, Santa Clara, California, USA

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Arthur S Tischler Department of Pathology and Laboratory Medicine, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA

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al. 2018 ). In contrast to mice and other species, rats have an unusual proclivity to develop PCs. The incidence of these tumors increases throughout life and is especially high in males compared to females, with a ratio up to 10:1 in some rat

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-19-0474
Volume/Issue:
Volume 27: Issue 6
Open access
Kirsten L Dennison McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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Nyssa Becker Samanas McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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Quincy Eckert Harenda McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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Maureen Peters Hickman McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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Nicole L Seiler McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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Lina Ding McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health
McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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James D Shull McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health
McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health
McArdle Laboratory for Cancer Research, School of Medicine and Public Health, School of Medicine and Public Health, Department of Oncology, School of Medicine and Public Health

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large fraction of breast cancers, the molecular mechanisms through which estrogens contribute to breast cancer etiology remain poorly defined. The ACI rat model of 17β-estradiol (E 2 )-induced mammary cancer serves as a unique and physiologically

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-14-0539
Volume/Issue:
Volume 22: Issue 2
Free access
Fabiana Cillo
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Magda de Eguileor
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Fulvio Gandolfi
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Tiziana A L Brevini
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these observations, in the present paper, we investigated the effect of A-1254 in rat prostate cells. These cultures were used as an in vitro model for investigating the possible mechanism involved in detrimental effects of PCBs on prostate, which

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-06-0081
Volume/Issue:
Volume 14: Issue 2
Free access
A G Mackay
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E A Ofori-Kuragu
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A Lansdown
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R C Coombes
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L Binderup
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K W Colston
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Abstract

The anti-tumour effect of EB 1089, a novel vitamin D analogue with reduced calcaemic activity, was examined in vivo using the N-methyl-nitrosourea-induced rat mammary tumour model. The vitamin D compound was given orally at a dose of 1 pg/kg body weight alone and in combination with tamoxifen (1 mg/kg). Effects were compared with oral tamoxifen treatment alone. EB 1089 significantly inhibited tumour progression compared with controls with a response rate of 58% and a regression rate of 92% As expected, tamoxifen at the dose given also caused significant inhibition of tumour progression with a response rate of 73%. Combination of these two compounds did not lead to a marked increase in their effectiveness. Histological examination of tumours from EB 1089-treated rats showed a marked reduction in cellularity and mitotic activity.

At the dose given, EB 1089 produced a significant rise in serum calcium concentration and urinary calcium excretion. Tamoxifen treatment alone did not significantly alter serum calcium levels. However, combined treatment with tamoxifen and EB 1089 led to a significant reduction in hypercalcaemia compared with EB 1089 alone. It is suggested that vitamin D analogues with reduced calcaemic activity may provide a new therapeutic strategy for certain malignancies, either alone or in combination with established treatment regimens.

Endocrine-Related Cancer (1996) 3 327-335

Article Type:
Research Article
DOI:
https://doi.org/10.1677/erc.0.0304327
Volume/Issue:
Volume 3: Issue 4
Restricted access
Anne Wierinckx
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Carole Auger
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Pauline Devauchelle
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Arlette Reynaud
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Pascale Chevallier
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Michel Jan
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Gilles Perrin
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Michelle Fèvre-Montange
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Catherine Rey
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Dominique Figarella-Branger
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Gérald Raverot
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Marie-Françoise Belin
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Joël Lachuer
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Jacqueline Trouillas
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approaches in human tumors and a tumor rat model as previously described ( Trouillas et al. 1990 , 1999 ). We used 25 human PRL tumors carefully classified into three groups (non-invasive, invasive, and aggressive–invasive) by radiology using magnetic

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-07-0062
Volume/Issue:
Volume 14: Issue 3
Free access
Misu Lee Institute for Diabetes and Cancer, Helmholtz Zentrum München, Neuherberg, Germany

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Ninelia Minaskan Institute for Diabetes and Cancer, Helmholtz Zentrum München, Neuherberg, Germany

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Tobias Wiedemann Institute for Diabetes and Cancer, Helmholtz Zentrum München, Neuherberg, Germany

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Martin Irmler Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany

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Johannes Beckers Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany
German Center for Diabetes Research (DZD), Neuherberg, Germany
Technische Universität München, Chair of Experimental Genetics, Freising, Germany

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Behrooz H Yousefi Department of Pharmaceutical Radiochemistry, Technische Universität München, Garching, Germany

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Georgios Kaissis Institute for Diagnostic and Interventional Radiology, Klinikum rechts der Isar der Technische Universität München, Munich, Germany

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Rickmer Braren Institute for Diagnostic and Interventional Radiology, Klinikum rechts der Isar der Technische Universität München, Munich, Germany

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Iina Laitinen Department of Nuclear Medicine, Klinikum rechts der Isar der Technische Universität München, Munich, Germany

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Natalia S Pellegata Institute for Diabetes and Cancer, Helmholtz Zentrum München, Neuherberg, Germany

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neoplasia syndrome in the rat, which is caused by a homozygous germline mutation in the Cdkn1b gene encoding the cell cycle inhibitor p27 ( Pellegata et al. 2006 ). MENX-affected rats develop, among other endocrine tumors, bilateral PCCs with complete

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-16-0324
Volume/Issue:
Volume 24: Issue 1
Free access
M Principe Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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M Chanal Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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V Karam Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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A Wierinckx Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France
ProfilXpert, Lyon, France

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I Mikaélian Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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R Gadet Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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C Auger Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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V Raverot Laboratoire d’Hormonologie, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Lyon, France

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E Jouanneau Service de Neurochirurgie, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France
Faculté de Médecine Lyon Est, Université Lyon 1, Lyon, France

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A Vasiljevic Faculté de Médecine Lyon Est, Université Lyon 1, Lyon, France
Department of Pathology, Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France

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A Hennino Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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G Raverot Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France
Department of Pathology, Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France
Department of Endocrinology, Reference Center for Rare Pituitary Disease (HYPO), Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France

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P Bertolino Cancer Research Centre of Lyon (CRCL), INSERM U1052, CNRS UMR5286, Claude Bernard University, Lyon, France

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instance, BMP4 is capable of stimulating the proliferation of GH3 cells, a rat prolactinoma-derived cell line ( Paez-Pereda et al . 2003 ), whereas TGFβ inhibits this effect and is further capable of repressing prolactin expression in both GH3 and GH4

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-18-0082
Volume/Issue:
Volume 25: Issue 9
Free access
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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, we have particularly focused on the NIS gene in this study as it is the most important gene for thyroid uptake of iodide. Materials and methods Cell culture and reagents Rat thyroid PCCL3 cell line and its transfectants were cultured and maintained

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-13-0399
Volume/Issue:
Volume 21: Issue 2
Open access
Aparna Lakshmanan 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
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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Anna Wojcicka 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
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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Marta Kotlarek 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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Xiaoli Zhang 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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Krystian Jazdzewski 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
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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Sissy M Jhiang 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
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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of NIS . The effect of this miR on NIS-mediated RAIU was assessed in MCF-7 human breast cancer cells and PCCl3 rat thyroid cells. Direct binding of this miR to the 3′UTR of h NIS was verified by luciferase-h NIS -3′UTR reporter assay. In the second

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-14-0439
Volume/Issue:
Volume 22: Issue 1
Free access
Lilja E Laatikainen Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Maria D Castellone Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Aline Hebrant Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Candice Hoste Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Maria C Cantisani Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Juha P Laurila Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Giuliana Salvatore Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Paolo Salerno Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Fulvio Basolo Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Johnny Näsman Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Jacques E Dumont Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Massimo Santoro Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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Mikko O Laukkanen Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland
Cellular Therapy Group, Institute of Experimental Endocrinology and Oncology (CNR), Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali, Dipartimento di Chirurgia, Åbo Akademi University, Fondazione IRCCS SDN, Medicity Research Laboratory, University of Turku, Tykistökatu 6A, FIN-20520 Turku, Finland

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(University of Turku, Turku, Finland) were given 0.25% propylthiouracil (PTU; Sigma) ad libitum in drinking water for 2 weeks, killed, and tissues were collected for expression analysis. As controls for histological staining, we used nontreated rat thyroids

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-10-0021
Volume/Issue:
Volume 17: Issue 3
Free access