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focused on better understanding of androgen receptor (AR) signaling with our current knowledge being largely derived from experimental cell culture and animal models. In vitro cell cultures have the advantage of being relatively cheap and typically have
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-microtubule drugs and the spindle-targeting inhibitors. By further comparing the cell culture results with those from mouse tumor models, we would discuss potential therapeutic and toxic mechanisms of anti-mitotic drugs seen in the clinic. In our discussion of
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models. This paper describes a unique PDX and cell culture model for basic and pre-clinical studies of SDH-deficient GIST. The model, which we have named ‘the Ian GIST model’, is derived from an aggressive gastric GIST that arose in a young man with a
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the functional and growth properties of long-term cell cultures of an SST-secreting cancer (SS-C cells) obtained from a primary human somatostatinoma. We also evaluated the response of SS-C cells to various physiological and pharmacological agents
Maimonides Institute for Biomedical Research of Cordoba (IMIBIC), Córdoba, Spain
Reina Sofia University Hospital, Córdoba, Spain
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Reina Sofia University Hospital, Córdoba, Spain
Department of Cell Biology, Physiology, and Immunology, University of Córdoba, Córdoba, Spain
CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Córdoba, Spain
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). Most cell-based assays use traditional 2D monolayer cell cultures on flat, rigid substrates. 2D monolayer cultures have some limitations, and it has been recognized that the effectiveness of drugs in 2D monolayer in vitro culture systems are often not
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia
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Department of Microbiology, Dankook University, Cheonan, Republic of Korea
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Department Pharmazie, Ludwig-Maximilians-Universität München, Munich, Germany
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Department of Medicine, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, District of Columbia, USA
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transcriptional consequences and cancer progenitor cell retention of two different primary cancer epithelial cell culture methodologies: the mammary epithelial cell-optimized EpiCult (B) system (Stemcell Technologies, Vancouver, BC, Canada) ( Yamaji et al. 2009
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far the most commonly used cell culture models of prostate cancer ( Bosland et al. 1996 ). Although other prostate cancer cell lines are available, recent studies revealed that many of these are in fact derivatives of the three aforementioned cell
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Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
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develop PCCs, we hypothesized that rats would a priori be superior to mice as a potential Sdhb tumor model. This communication describes the successful development of a new rat-derived xenograft and cell culture model that closely mirrors the
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Neuroendocrinology Group, Neurosurgical Clinic, Department of Neurosurgery, Neurosurgical Clinic, Neurosurgical Clinic, Department of Internal Medicine 1 and Clinical Chemistry, Laboratorio de Fisiología y Biología Molecular, IFIBYNE-CONICET, Max Planck Institute of Psychiatry, Kraepelinstrasse 10, D-80804 Munich, Germany
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Neuroendocrinology Group, Neurosurgical Clinic, Department of Neurosurgery, Neurosurgical Clinic, Neurosurgical Clinic, Department of Internal Medicine 1 and Clinical Chemistry, Laboratorio de Fisiología y Biología Molecular, IFIBYNE-CONICET, Max Planck Institute of Psychiatry, Kraepelinstrasse 10, D-80804 Munich, Germany
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time about the role of curcumin in vivo in experimentally induced pituitary tumours of nude mice and in primary cell cultures of human pituitary adenomas. Materials and methods Materials Cell culture materials and reagents were obtained from Life
The Ohio State University and Arthur G. James Comprehensive Cancer Center, Columbus, Ohio, USA
Center for Cancer Engineering, The Ohio State University, Columbus, Ohio, USA
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Center for Cancer Engineering, The Ohio State University, Columbus, Ohio, USA
Division of Surgical Oncology, The Ohio State University and Arthur G. James Comprehensive Cancer Center, Columbus, Ohio, USA
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platforms using human cells for mechanistic research can complement traditional animal models and 2D cell cultures. The creation of accurate 3D models that mimic human cell–cell, cell–extracellular matrix (ECM), and mechanical interactions of in vivo