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Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5998, pp. 1492 - 1499
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 12/2009, Volume 119, Issue 12, pp. 3626 - 3636
The polycomb group protein B lymphoma Mo-MLV insertion region 1 homolog (Bmi-1) is dysregulated in various cancers, and its upregulation strongly correlates... 
MEDICINE, RESEARCH & EXPERIMENTAL | BREAST-CANCER CELLS | DEVELOPMENTAL REGULATORS | CELLULAR MEMORY | E-CADHERIN EXPRESSION | HEMATOPOIETIC STEM-CELLS | PROSTATE-CANCER | MYC TRANSGENIC MICE | SELF-RENEWAL | NF-KAPPA-B | TRANSCRIPTION FACTOR | Nasopharyngeal Neoplasms - genetics | Neoplasm Transplantation | Nasopharyngeal Neoplasms - metabolism | Epithelial Cells - metabolism | Cadherins - metabolism | Humans | Glycogen Synthase Kinase 3 beta | Transplantation, Heterologous | Phosphatidylinositol 3-Kinases - metabolism | Mesoderm - cytology | Repressor Proteins - antagonists & inhibitors | Nasopharyngeal Neoplasms - pathology | Cadherins - genetics | Epithelial Cells - cytology | Nuclear Proteins - genetics | Proto-Oncogene Proteins c-akt - metabolism | Nasopharyngeal Neoplasms - etiology | Snail Family Transcription Factors | Nasopharynx - metabolism | Repressor Proteins - metabolism | Proto-Oncogene Proteins - metabolism | PTEN Phosphohydrolase - genetics | Proto-Oncogene Proteins - antagonists & inhibitors | Signal Transduction | Neoplasm Invasiveness | Down-Regulation | Gene Silencing | PTEN Phosphohydrolase - metabolism | Repressor Proteins - genetics | Nuclear Proteins - metabolism | Proto-Oncogene Proteins - genetics | Glycogen Synthase Kinase 3 - metabolism | Transcription Factors - metabolism | Animals | Polycomb Repressive Complex 1 | Mice, Nude | Nuclear Proteins - antagonists & inhibitors | Cell Line, Tumor | Mesoderm - metabolism | Mice | Nasopharynx - cytology | Chromatin | Care and treatment | Lymphomas | Research | Analysis | Cancer | Index Medicus | Abridged Index Medicus
Journal Article
Nature Medicine, ISSN 1078-8956, 11/2015, Volume 21, Issue 11, pp. 1262 - 1271
Cancer-associated muscle weakness is a poorly understood phenomenon, and there is no effective treatment. Here we find that seven different mouse models of... 
MEDICINE, RESEARCH & EXPERIMENTAL | CANCER CACHEXIA | CELLS | INTRACELLULAR CALCIUM | BIOCHEMISTRY & MOLECULAR BIOLOGY | RELEASE | CELL BIOLOGY | DYSTROPHIC MUSCLE | GROWTH-FACTOR-BETA | HORMONE-RELATED PROTEIN | RYANODINE RECEPTOR | CAMURATI-ENGELMANN-DISEASE | IN-VIVO | Neoplasms - metabolism | Prostatic Neoplasms - metabolism | Up-Regulation | Calcium - metabolism | Humans | Lung Neoplasms - metabolism | NADPH Oxidases - metabolism | Bone Neoplasms - secondary | Lung Neoplasms - pathology | Male | Muscle, Skeletal - metabolism | Osteolysis - etiology | Ryanodine Receptor Calcium Release Channel - metabolism | X-Ray Microtomography | Bone Neoplasms - metabolism | Breast Neoplasms - metabolism | Neoplasms - complications | MCF-7 Cells | Osteolysis - diagnostic imaging | Muscle Proteins - metabolism | NADPH Oxidases - genetics | Female | Camurati-Engelmann Syndrome - metabolism | Muscle Strength | Calcium Signaling | Disease Models, Animal | Muscle Weakness - etiology | Prostatic Neoplasms - pathology | Oxidation-Reduction | Bone Neoplasms - diagnostic imaging | NADPH Oxidase 4 | Mice, SCID | Multiple Myeloma - metabolism | Absorptiometry, Photon | Osteolysis - metabolism | Multiple Myeloma - pathology | Animals | Muscle Contraction | Breast Neoplasms - pathology | Mice, Nude | Muscle Weakness - metabolism | Cell Line, Tumor | Mice | Neoplasms - pathology | Transforming Growth Factor beta - metabolism | Index Medicus
Journal Article
Cancer Cell, ISSN 1535-6108, 07/2014, Volume 26, Issue 1, pp. 121 - 135
The tumor microenvironment plays a critical role in cancer progression, but the precise mechanisms by which stromal cells influence the epithelium are poorly... 
CELLS | ACTIVATION | INVASION | TGF-BETA | ONCOLOGY | REACTIVE STROMA | PATHWAY | PROTEIN P62 | PROSTATE-CANCER | AUTOPHAGY | TUMOR-GROWTH | CELL BIOLOGY | Inflammation - pathology | Fibroblasts - enzymology | Prostatic Intraepithelial Neoplasia - pathology | Oxidative Stress | TOR Serine-Threonine Kinases - metabolism | Sequestosome-1 Protein | Stromal Cells - pathology | Coculture Techniques | Humans | Tumor Microenvironment | Male | Multiprotein Complexes - genetics | Heat-Shock Proteins - deficiency | Heat-Shock Proteins - genetics | Multiprotein Complexes - metabolism | TOR Serine-Threonine Kinases - genetics | RNA Interference | Time Factors | Cell Transformation, Neoplastic - genetics | Interleukin-6 - metabolism | Fibroblasts - metabolism | PTEN Phosphohydrolase - genetics | Signal Transduction | Prostatic Hyperplasia - genetics | Mice, Knockout | Energy Metabolism | Prostatic Intraepithelial Neoplasia - enzymology | Adaptor Proteins, Signal Transducing - deficiency | Cell Line, Tumor | Glucose - metabolism | Mice | Proto-Oncogene Proteins c-myc - genetics | Prostatic Hyperplasia - enzymology | Prostatic Intraepithelial Neoplasia - genetics | Inflammation - enzymology | Prostatic Hyperplasia - pathology | Mechanistic Target of Rapamycin Complex 1 | Amino Acids - metabolism | Stromal Cells - enzymology | Prostatic Neoplasms - genetics | Transfection | HEK293 Cells | Inflammation Mediators - metabolism | Prostatic Neoplasms - pathology | Neoplasm Invasiveness | Heat-Shock Proteins - metabolism | Mice, Inbred C57BL | Cell Communication | PTEN Phosphohydrolase - metabolism | Cell Transformation, Neoplastic - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Animals | Adaptor Proteins, Signal Transducing - genetics | Inflammation - genetics | Prostatic Neoplasms - enzymology | Adaptor Proteins, Signal Transducing - metabolism | Cell Transformation, Neoplastic - pathology | Glucose metabolism | Development and progression | Glucose | Prostate cancer | Dextrose | Tumors | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2012, Volume 109, Issue 23, pp. 8983 - 8988
In addition to glycolysis, the oncogenic transcription factor c-MYC (MYC) stimulates glutamine catabolism to fuel growth and proliferation of cancer cells... 
T lymphocytes | Cell growth | Energy metabolism | Cellular metabolism | Small interfering RNA | Catabolism | Biosynthesis | Tumors | Cancer | Apoptosis | Amino acids | miRNA | Reactive oxygen species | Metabolic tumor suppressor | Redox signaling | APOPTOSIS | MULTIDISCIPLINARY SCIENCES | amino acids | CELL-GROWTH | HYPOXIA | CANCER | B-CELLS | PYRROLINE-5-CARBOXYLIC ACID | redox signaling | OXIDASE | GENE | reactive oxygen species | TUMOR-SUPPRESSOR | CARBOXYLATION | metabolic tumor suppressor | Gas Chromatography-Mass Spectrometry | Reactive Oxygen Species - metabolism | Nitrogen Isotopes - metabolism | Oxidation-Reduction | Proline - metabolism | Pyrroline Carboxylate Reductases - metabolism | Humans | Glutamine - metabolism | MicroRNAs - metabolism | Carbon Isotopes - metabolism | Gene Expression Regulation, Enzymologic - physiology | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Gene Knockdown Techniques | DNA-Binding Proteins - metabolism | Transcription Factors - metabolism | Chromatin Immunoprecipitation | Gene Expression Regulation, Enzymologic - genetics | Cell Line, Tumor | Nuclear Magnetic Resonance, Biomolecular | Proline Oxidase - metabolism | Real-Time Polymerase Chain Reaction | Cell proliferation | Transcription factors | Proline | Cell metabolism | Genetic aspects | Properties | Glutamine | Metabolism | Prostate cancer | Index Medicus | Biological Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2017, Volume 12, Issue 6, pp. e0179610 - e0179610
Objective To assess the prognostic roles of BAP1, PBRM1, pS6, PTEN, TGase2, PD-L1, CA9, PSMA, and Ki-67 tissue biomarkers in localized renal cell carcinoma... 
SURVIVAL | MORTALITY | CARBONIC-ANHYDRASE-IX | PROTEIN | MULTIDISCIPLINARY SCIENCES | CANCER INCIDENCE | METASTASES | OUTCOMES | KI67 | EXPRESSION | TUMORS | Immunohistochemistry | Prognosis | Tissue Array Analysis | Humans | Middle Aged | Ki-67 Antigen - metabolism | Male | Kidney Neoplasms - metabolism | Porphyrins - metabolism | Neoplasm Recurrence, Local - mortality | Neoplasm Recurrence, Local - pathology | Glutamate Carboxypeptidase II - metabolism | Neoplasm Grading | Antigens, Neoplasm - metabolism | Antigens, Surface - metabolism | Biomarkers, Tumor - metabolism | Ubiquitin Thiolesterase - metabolism | Adult | Female | Carbonic Anhydrase IX - metabolism | Retrospective Studies | Tumor Suppressor Proteins - metabolism | Neoplasm Recurrence, Local - metabolism | Carcinoma, Renal Cell - pathology | PTEN Phosphohydrolase - metabolism | Nuclear Proteins - metabolism | Survival Rate | Kidney Neoplasms - mortality | Transcription Factors - metabolism | Carcinoma, Renal Cell - metabolism | Carcinoma, Renal Cell - mortality | Disease-Free Survival | B7-H1 Antigen - metabolism | Transglutaminases - metabolism | Sulfonamides - metabolism | Kidney Neoplasms - pathology | Aged | Neoplasm Staging | GTP-Binding Proteins - metabolism | Genetic aspects | Carcinoma, Renal cell | Research | Biological markers | Biometrics | Slopes | Metastasis | Kinases | Epidemiology | Cancer therapies | Urology | Proteins | Nephrectomy | Quality | Bioindicators | Growth factors | Age | Antigens | Markers | Hazards | Patients | Survival | Disease prevention | Hospitals | Medical prognosis | PD-L1 protein | Biomarkers | Death | Mutation | Diabetes | Prostate cancer | PTEN protein | Clear cell-type renal cell carcinoma | Cancer | Kidney transplantation | Tumors | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, pp. e34653 - e34653
Background: Shedding microvesicles are membrane released vesicles derived directly from the plasma membrane. Exosomes are released membrane vesicles of late... 
CA2&-STIMULATED ADENOSINE-TRIPHOSPHATASE | HUMAN PROSTATIC FLUID | EPITHELIAL-CELLS | MEMBRANE-VESICLES | BIOLOGY | HUMAN SEMEN | SPERMATOZOA | EXTRACELLULAR ORGANELLES PROSTASOMES | SECRETION | TUMOR-DERIVED EXOSOMES | HUMAN SPERM | Exosomes - metabolism | Cell Line | NIH 3T3 Cells | Microscopy, Electron, Transmission - methods | Secretory Vesicles - metabolism | DNA - metabolism | RNA, Messenger - metabolism | Clathrin - metabolism | Animals | Cell Nucleus - metabolism | Biological Transport | Myocytes, Cardiac - metabolism | Cytosol - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Mice | Annexin A2 - metabolism | Caveolin 3 - metabolism | Fibroblasts - metabolism | RNA - metabolism | Clathrin | RNA | Genes | Hostages | Nucleotide sequencing | Gene expression | DNA sequencing | Heart | Flow cytometry | Sperm | Centrifugation | Lung cancer | Ultracentrifugation | Biochemistry | Exosomes | Cytosol | Nuclei | Muscular dystrophy | Gene sequencing | Vesicles | Rodents | Penicillin | Fibroblasts | Public health | Deoxyribonucleic acid--DNA | Messages | Nucleotide sequence | Caveolin | Membrane vesicles | Cardiomyocytes | Electron microscopy | Metabolism | Medicine | Polymerase | DNA nucleotidylexotransferase | Cytometry | Hospitals | Transmission electron microscopy | Ribonucleic acids | MicroRNAs | Media (differential) | Biochemical characteristics | Clinical medicine | Mutation | Prostate | Index Medicus | Cell and Molecular Biology | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Cell- och molekylärbiologi | Medicinska och farmaceutiska grundvetenskaper | Deoxyribonucleic acid | DNA
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 02/2016, Volume 59, Issue 4, pp. 1271 - 1298
Bromodomains, small protein modules that recognize acetylated lysine on histones, play a significant role in the epigenome, where they function as "readers"... 
CHEMISTRY, MEDICINAL | SWI/SNF COMPLEXES | SMALL-MOLECULE INHIBITORS | PROSTATE-CANCER | SELECTIVE INHIBITORS | GENE-EXPRESSION | CHEMICAL PROBE | TUMOR-SUPPRESSOR | BET INHIBITORS | HISTONE ACETYLTRANSFERASE | PHD FINGER | Small Molecule Libraries - pharmacology | Antigens, Nuclear - metabolism | Humans | Drug Discovery - methods | CREB-Binding Protein - antagonists & inhibitors | Chromosomal Proteins, Non-Histone - antagonists & inhibitors | DNA-Binding Proteins - metabolism | CREB-Binding Protein - metabolism | Protein Processing, Post-Translational - drug effects | Adaptor Proteins, Signal Transducing - antagonists & inhibitors | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Lysine - metabolism | Protein-Serine-Threonine Kinases - metabolism | RNA-Binding Proteins - antagonists & inhibitors | Nerve Tissue Proteins - antagonists & inhibitors | ATPases Associated with Diverse Cellular Activities | DNA-Binding Proteins - antagonists & inhibitors | Chromosomal Proteins, Non-Histone - metabolism | Carrier Proteins - antagonists & inhibitors | Adenosine Triphosphatases - metabolism | Models, Molecular | Nuclear Proteins - metabolism | Transcription Factors - antagonists & inhibitors | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Adenosine Triphosphatases - antagonists & inhibitors | DNA Helicases - metabolism | Small Molecule Libraries - chemistry | Acetylation - drug effects | Animals | Carrier Proteins - metabolism | Nuclear Proteins - antagonists & inhibitors | DNA Helicases - antagonists & inhibitors | Histones - metabolism | Adaptor Proteins, Signal Transducing - metabolism | RNA-Binding Proteins - metabolism | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2009, Volume 106, Issue 30, pp. 12465 - 12470
Chromosomal rearrangements involving erythroblast transformation specific (ETS) family transcription factors were recently defined as the most common genetic... 
Adenocarcinoma | Prostate gland | Epithelial cells | Cell lines | Mice | Lesions | Prostate | Prostate cancer | Cells | Tissue grafting | PTEN | AKT | ERG | Androgen receptor | TRANSFORMATION | STEM-CELLS | MULTIDISCIPLINARY SCIENCES | CANCER | prostate cancer | androgen receptor | RECURRENT GENE FUSIONS | TMPRSS2-ERG FUSION | IN-VIVO | MOUSE MODEL | Immunohistochemistry | Transcriptional Regulator ERG | Oncogene Proteins - genetics | Prostatic Neoplasms - metabolism | Prostatic Intraepithelial Neoplasia - pathology | Epithelial Cells - metabolism | Proto-Oncogene Proteins c-ets - genetics | Hyperplasia | Male | Phosphatidylinositol 3-Kinases - metabolism | Prostate - metabolism | Tumor Suppressor Protein p53 - genetics | DNA-Binding Proteins - metabolism | Prostate - pathology | Prostatic Neoplasms - genetics | Proto-Oncogene Proteins c-ets - metabolism | Prostatic Intraepithelial Neoplasia - metabolism | Prostatic Neoplasms - pathology | Signal Transduction | Mice, Inbred C57BL | Cells, Cultured | Oncogene Proteins - metabolism | Tumor Suppressor Protein p53 - metabolism | Epithelial Cells - pathology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Proto-Oncogene Proteins c-myc - metabolism | Blotting, Western | Transcription Factors - metabolism | Integrin alpha6 - metabolism | Animals | Cell Transformation, Neoplastic | Proto-Oncogene Proteins c-jun - metabolism | Keratin-5 - metabolism | Luminescent Proteins - genetics | Mutation | Prostatic Intraepithelial Neoplasia - genetics | Luminescent Proteins - metabolism | Androgens | Physiological aspects | Development and progression | Genetic aspects | Cellular signal transduction | DNA binding proteins | Research | Proteins | Genes | Genetics | Chromosomes | Tumors | Index Medicus | Biological Sciences
Journal Article
Molecular Carcinogenesis, ISSN 0899-1987, 02/2014, Volume 53, Issue 2, pp. 85 - 97
As a link between inflammation and cancer has been reported in many studies, we established an in vitro model of prostatic inflammation to investigate the loss... 
androgen | loss of p53 | inflammation | DNA damage | ROS | prostate | NFkB | Loss of p53 | Androgen | Inflammation | Prostate | SURVIVAL | OXIDATIVE STRESS | CANCER CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUTATHIONE-PEROXIDASE | CARCINOGENESIS | ONCOLOGY | NKX3.1 | CARCINOMAS | LINK | HOMEOBOX GENE | EXPRESSION | Proto-Oncogene Proteins c-mdm2 - genetics | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Antioxidants - metabolism | Homeodomain Proteins - metabolism | Humans | Transcriptional Activation - drug effects | Tumor Necrosis Factor-alpha - genetics | Apoptosis - genetics | Male | NF-kappa B - metabolism | Interleukin-1beta - genetics | Prostatitis - metabolism | Inflammation - metabolism | Matrix Metalloproteinase 9 - metabolism | Phosphorylation - genetics | Acetylcysteine - analogs & derivatives | Interleukin-1beta - metabolism | Matrix Metalloproteinase 9 - genetics | U937 Cells | Prostate-Specific Antigen - metabolism | Phosphorylation - drug effects | Interleukin-6 - metabolism | Prostate-Specific Antigen - genetics | Glutathione Peroxidase - metabolism | Lysine - analogs & derivatives | Interleukin-6 - genetics | Down-Regulation - genetics | Glutathione Peroxidase - genetics | Prostatitis - drug therapy | Androgens - genetics | Macrophages - metabolism | Receptors, Androgen - genetics | Signal Transduction - drug effects | Cell Line, Tumor | Androgens - metabolism | Tumor Necrosis Factor-alpha - metabolism | Prostatic Neoplasms - metabolism | Receptors, Androgen - metabolism | I-kappa B Proteins - metabolism | I-kappa B Proteins - genetics | Prostatitis - pathology | Tumor Suppressor Protein p53 - genetics | Cell Differentiation - genetics | Prostatic Neoplasms - genetics | Inflammation Mediators - metabolism | Proto-Oncogene Proteins c-mdm2 - metabolism | Prostatic Neoplasms - pathology | Kallikreins - genetics | Tumor Suppressor Protein p53 - metabolism | Antioxidants - pharmacology | Transcription Factors - genetics | Down-Regulation - drug effects | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Up-Regulation - drug effects | Lysine - pharmacology | NF-kappa B - genetics | Cell Differentiation - drug effects | Acetylcysteine - pharmacology | Inflammation - genetics | Macrophages - drug effects | Kallikreins - metabolism | Ubiquitin | Analysis | Kallikrein | Hormones, Sex | Tumor proteins | Mitogens | Androgens | Cytokines | Molecular biology | Gene expression | Prostate cancer | Index Medicus
Journal Article