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Eyun Song Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Dong Eun Song Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Jonghwa Ahn Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Tae Yong Kim Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Won Bae Kim Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Young Kee Shong Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Min Ji Jeon Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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Won Gu Kim Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Republic of Korea

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lymph node metastases, and increased cancer-related mortality ( Kim et al. 2012 , Li et al. 2012 , Xing et al. 2013 ). Genetic alterations involving RAS -family genes comprise another distinct feature of DTCs ( Nikiforov 2008 , Prior et al

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-19-0452
Volume/Issue:
Volume 27: Issue 5
Restricted access
Mírian Romitti Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Simone Magagnin Wajner Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Lucieli Ceolin Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Carla Vaz Ferreira Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Rafaela Vanin Pinto Ribeiro Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Helena Cecin Rohenkohl Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Shana de Souto Weber Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Patrícia Luciana da Costa Lopez Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Cesar Seigi Fuziwara Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Edna Teruko Kimura Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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Ana Luiza Maia Thyroid Section, Experimental Research Center, Department of Cell and Developmental Biology, Endocrine Division, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2350, CEP 90035‐003 Porto Alegre, RS, Brazil

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MAPK genetic alterations on the DIO3 levels in 25 human PTC samples. Clinical and oncological features are detailed in Table 1 . Mean age of patients was 37.04±14.7 years, and 76% were women. The median tumor size was 2.5 cm (0.8–10.5); 13 patients

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-15-0162
Volume/Issue:
Volume 23: Issue 3
Free access
Jamie L Van Etten Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA

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Scott M Dehm Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA
Department of Urology, University of Minnesota, Minneapolis, MN, USA

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Nowell in 1976 based on cytogenetic data ( Nowell 1976 ). In this early model, a cell of origin acquires genetic alterations that promote neoplasia. Further genetic instability fuels clonal expansion of “fit” clones that ultimately leads to advanced

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-16-0049
Volume/Issue:
Volume 23: Issue 4
Free access
Yangang Wang Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA
Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Meiju Ji Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Wei Wang Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Zhimin Miao Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Peng Hou Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Xinyan Chen Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Feng Xu Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Guangwu Zhu Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Xianlu Sun Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Yujun Li Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Steven Condouris Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The 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 and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Shengli Yan Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Jie Pan Division of Endocrinology and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The 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 and Metabolism, Affilated Hospital of Qingdao University School of Medicine, The Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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et al . 2006 ). This increase is virtually completely attributed to the diagnosis of papillary thyroid cancer (PTC), which accounts for ∼80% of all thyroid cancers. As in other human cancers, genetic alterations are the driving force for PTC

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-07-0182
Volume/Issue:
Volume 15: Issue 1
Free access
Xiaoli Liu
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Justin Bishop Laboratory for Cellular and Molecular Thyroid Research, Department of Pathology, Departments of Anatomic Pathology and Neuro-Oncology, Department of Otolaryngology–Head and Neck Surgery, Jilin Provincial Key Laboratory of Surgical Translational Medicine, Department of Pathology, Division of Endocrinology and Metabolism, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Yuan Shan Laboratory for Cellular and Molecular Thyroid Research, Department of Pathology, Departments of Anatomic Pathology and Neuro-Oncology, Department of Otolaryngology–Head and Neck Surgery, Jilin Provincial Key Laboratory of Surgical Translational Medicine, Department of Pathology, Division of Endocrinology and Metabolism, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Sara Pai Laboratory for Cellular and Molecular Thyroid Research, Department of Pathology, Departments of Anatomic Pathology and Neuro-Oncology, Department of Otolaryngology–Head and Neck Surgery, Jilin Provincial Key Laboratory of Surgical Translational Medicine, Department of Pathology, Division of Endocrinology and Metabolism, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Dingxie Liu
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Avaniyapuram Kannan Murugan
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Hui Sun Laboratory for Cellular and Molecular Thyroid Research, Department of Pathology, Departments of Anatomic Pathology and Neuro-Oncology, Department of Otolaryngology–Head and Neck Surgery, Jilin Provincial Key Laboratory of Surgical Translational Medicine, Department of Pathology, Division of Endocrinology and Metabolism, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Adel K El-Naggar Laboratory for Cellular and Molecular Thyroid Research, Department of Pathology, Departments of Anatomic Pathology and Neuro-Oncology, Department of Otolaryngology–Head and Neck Surgery, Jilin Provincial Key Laboratory of Surgical Translational Medicine, Department of Pathology, Division of Endocrinology and Metabolism, Johns Hopkins University School of Medicine, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287, USA

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Mingzhao Xing
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, cancer-specific somatic genetic alterations, further supporting their potentially important role in human tumorigenesis. This is consistent with the previously observed increased telomerase activities in some human cancers ( Smekalova et al . 2012

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-13-0210
Volume/Issue:
Volume 20: Issue 4
Free access
Jacob A Quaytman Division of General Internal Medicine, Department of Medicine, University of Pittsburgh, UPMC Montefiore Hospital, N715, Pittsburgh, PA, USA

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Yuri E Nikiforov Division of Molecular Genomic Pathology, Department of Pathology, University of Pittsburgh, Pittsburgh, PA, USA

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Marina N Nikiforova Division of Endocrinology and Metabolism, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA

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Elena Morariu Division of Endocrinology and Metabolism, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA

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( Nicholson et al. 2019 ). However, to take full advantage of molecular testing, more information is needed on the outcomes of thyroid nodules with various genetic alterations. The results of this study show that patients with isolated PTEN mutations are

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-22-0061
Volume/Issue:
Volume 29: Issue 9
Restricted access
Kyle M Walsh
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Murim Choi Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Kjell Oberg Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Matthew H Kulke Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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James C Yao Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Chengqing Wu
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Magdalena Jurkiewicz
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Ling-I Hsu
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Susanne M Hooshmand Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Manal Hassan Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Eva T Janson Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Janet L Cunningham Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Evan Vosburgh Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Richard S Sackler Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Richard P Lifton Department of Epidemiology and Public Health, Department of Genetics, Department of Endocrine Oncology, Department of Medical Oncology, Department of Gastrointestinal Medical Oncology, Verto Institute, Yale University, 60 College Street, New Haven, Connecticut 06520, USA

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Andrew T DeWan
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Josephine Hoh
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list of the most commonly reported chromosomal alterations was compiled, and a meta-analysis of the prevalence of this alteration in patients with ileal carcinoids was performed. As different genetic alterations may distinguish localized ileal carcinoid

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-10-0248
Volume/Issue:
Volume 18: Issue 1
Free access
Laura Sterian Ward Laboratory of Cancer Molecular Genetics, Faculty of Medical Sciences, University of Campinas (Unicamp), 126, Tessalia Vieira de Camargo Street, Cidade Universitaria, Campinas, Sao Paulo 13083-887, Brazil

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possible markers, such as genetic alterations in NTRK, TERT , and the fusion of the striatin ( STRN ) gene and anaplastic lymphoma kinase ( ALK ) gene. The authors point to a series of molecular markers that may define a molecular signature, not only

Article Type:
Editorial
DOI:
https://doi.org/10.1530/ERC-14-0407
Volume/Issue:
Volume 21: Issue 5
Free access
Nabahet Ameur CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Ludovic Lacroix CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit
CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Sophie Roucan CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Véronique Roux CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Sophie Broutin CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Monique Talbot CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Corinne Dupuy CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Bernard Caillou CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Martin Schlumberger CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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Jean-Michel Bidart CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit
CNRS FRE 2939, Translational Research Laboratory, Department of Nuclear Medicine and Endocrine Oncology, Functional Genomic Unit

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knowledge of induced genetic alterations in the various forms of MTC is essential for understanding the pathways involved in the development and progression of MTC with various phenotypes. It is also mandatory for the identification of molecular targets that

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-08-0289
Volume/Issue:
Volume 16: Issue 4
Free access
Barbora Bulanova Pekova Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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Vlasta Sykorova Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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Karolina Mastnikova Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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Eliska Vaclavikova Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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Jitka Moravcova Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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Petr Vlcek Department of Nuclear Medicine and Endocrinology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic

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Lucie Lancova Department of Nuclear Medicine and Endocrinology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic

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Petr Lastuvka Departments of Otorhinolaryngology and Head and Neck Surgery, 1st Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic

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Rami Katra Department of Ear, Nose and Throat, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic

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Petr Bavor Department of Surgery, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic

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Daniela Kodetova Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic

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Martin Chovanec Department of Otorhinolaryngology, 3rd Faculty of Medicine, University Hospital Kralovske Vinohrady, Prague, Czech Republic

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Jana Drozenova Department of Pathology, 3rd Faculty of Medicine, University Hospital Kralovske Vinohrady, Prague, Czech Republic

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Radoslav Matej Department of Pathology, 3rd Faculty of Medicine, University Hospital Kralovske Vinohrady, Prague, Czech Republic

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Jaromir Astl Department of Otorhinolaryngology and Maxillofacial Surgery, 3rd Faculty of Medicine and Military University Hospital, Prague, Czech Republic

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Jiri Hlozek Department of Otorhinolaryngology and Maxillofacial Surgery, 3rd Faculty of Medicine and Military University Hospital, Prague, Czech Republic

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Petr Hrabal Department of Pathology, Military University Hospital, Prague, Czech Republic

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Josef Vcelak Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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Bela Bendlova Department of Molecular Endocrinology, Institute of Endocrinology, Prague, Czech Republic

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genetic alterations found in thyroid cancer includes different types of mutations: somatic point mutations, indels, copy number alterations, and fusion genes ( Nikiforov 2011 ). Among the fusion genes, the most common and best known are RET (rearranged

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-23-0117
Volume/Issue:
Volume 30: Issue 12
Open access