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Cancer Center, Departments of Medicine, Department of Chemistry, Boston De Novo Design, K-701
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-specific susceptibility, designated ‘Ras-mediated apoptosis’, can be exploited as a targeted cancer therapeutic. Bronchopulmonary, gastrointestinal, and pancreatic neuroendocrine tumors are rare tumors originating from neuroendocrine tissues ( Oberg 1999 ). Clinical
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they almost never metastasize to the liver. Table 4 Functioning disease associated bronchopulmonary and gastroenteropancreatic neuroendocrine tumors (BP-NETs and GEP-NETs). Syndrome Prevalence (%) and type Hormone BP
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Deutsches Zentrum Immuntherapie DZI, Erlangen, Germany
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Introduction Neuroendocrine neoplasms (NENs) represent a rare and heterogeneous group of malignancies with variable tumor growth ( Pavel & Sers 2016 ). They occur with an estimated incidence of 6.98 cases/100,000 citizens ( Dasari et al
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Department of General, Visceral, Transplantation, Vascular and Thoracic Surgery, University-Hospital, Klinikum der Universität München, Ludwig-Maximilians-University of Munich, Munich, Germany
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experiments. Human bronchopulmonary neuroendocrine NCI-H727 tumor cells (p11 – p23 for main experiments) ( Cakir & Grossman 2011 ) (acquired from ATCC) and human midgut carcinoid GOT1 cells ( Kolby et al . 2001 ) (kindly provided by Prof. O Nilsson
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Introduction It is now widely accepted that peptide receptor radionuclide therapy (PRRT) is an effective treatment for inoperable or metastatic neuroendocrine tumors (NETs), particularly well-differentiated gastroenteropancreatic (GEP) or
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IGF1R and Hsp90 for development of novel anticancer drugs for, at a minimum, bronchopulmonary neuroendocrine tumors. Supplementary data This is linked to the online version of the paper at http://dx.doi.org/10.1677/ERC-09-0318 . Declaration of
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Introduction Bronchopulmonary (BP) neuroendocrine tumors (NETs; typical carcinoids and atypical carcinoids (TCs and ACs)) account for 20–25% of NETs and 1–2% of lung malignancies ( Öberg et al. 2012 , Filosso et al. 2018 , Baudin et al
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ENETS Center of Excellence, Neuroendocrine Tumour (NET) Center, Rome, Italy
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based on the common expression of the general markers of neuroendocrine differentiation chromogranin A and synaptophysin. NEN definition embraces the two families (classes) of the well-differentiated lesions, defined as neuroendocrine tumor (NET), and
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Drozdov I Joseph R Pfragner R Culler M Modlin I 2008 Differential cytotoxicity of novel somatostatin and dopamine chimeric compounds on bronchopulmonary and small intestinal neuroendocrine tumor cell lines . Cancer 113 690 – 700 . ( doi
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original articles, were included. The following search terms, alone or in combination, were used: ‘biomarkers’, ‘novel markers’, ‘neuroendocrine tumors’, ‘NETs’, ‘neuroendocrine neoplasms’, ‘NENs’, ‘circulating markers’, ‘tissue markers’, ‘therapeutic