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Introduction Historically, in vitro cultures of human prostatic cells have been limited in availability and scope compared with those from many other organs. Three spontaneously established cell lines, PC-3,DU145andLNCaP, are by
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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characteristics and progenitor cells from the original cancer are important goals for culture methodology. Genetically engineered mouse models (GEMM) of breast cancer serve as preclinical translational analogs for the study of breast cancer pathophysiology and
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
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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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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
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(D2R) and its isoforms (D2R long and D2R short ) mRNA, using real-time PCR on isolated adenoma cells, in culture. The functional role of these receptors was analyzed using [ 3 H]thymidine incorporation assay in the presence of various concentrations
University School of Nashville, Nashville, Tennessee, USA
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/spheroid culture that closely recapitulates patient responses may lead to novel therapeutic discoveries for BRAF-wildtype disease. In the current study, we show that eight thyroid cancer cell lines readily form spheroids that represent unique morphology and drug
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pancreatic PANC-1 cells have been used as a model to study the process of pancreatic islet formation. Following brief trypsin treatment and culturing in a chemically defined serum-free medium (SFM), cells formed islet-like cell aggregates and expressed the
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identifying stem cell populations in the normal WT prostate epithelium have identified multipotent basal cells using cell culture assays as well as renal graft methods that involve the transplantation of epithelial cells together with supporting urogenital
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Division of Endocrinology, Department of Pathology, Dipartimento di Scienze Mediche, IRCCS Istituto Auxologico Italiano, Department of Pathology, Department of Internal Medicine, Erasmus Medical Center, Erasmus MC, Dr Molewaterplein 50, 3015 GE Rotterdam, The Netherlands
Division of Endocrinology, Department of Pathology, Dipartimento di Scienze Mediche, IRCCS Istituto Auxologico Italiano, Department of Pathology, Department of Internal Medicine, Erasmus Medical Center, Erasmus MC, Dr Molewaterplein 50, 3015 GE Rotterdam, The Netherlands
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observed in primary adrenal hyperplasia cells and adrenocortical adenoma (ACA) cultures. Finally, the interaction between the effects of IFN-β and IGF2 in primary ACC cultures was evaluated. Materials and methods Patients Adrenal tissue samples for in