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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 | OXIDATIVE STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUTATHIONE-PEROXIDASE | CANCER | ONCOLOGY | GENES | NKX3.1 | LINK | 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
Oncogene, ISSN 0950-9232, 02/2015, Volume 34, Issue 44, pp. 5548 - 5559
Journal Article
European Urology, ISSN 0302-2838, 2016, Volume 71, Issue 5, pp. 776 - 787
Abstract Background Novel therapies for men with castration-resistant prostate cancer (CRPC) are needed, particularly for cancers not driven by androgen... 
Urology | Castration-resistance | Bone metastasis | Immune response | Metabolism | Prostate cancer | THERAPEUTICS | CLASS-I ANTIGENS | INFILTRATION | DENSITY | MELANOMA | REGULATORY T-CELLS | UROLOGY & NEPHROLOGY | UP-REGULATION | EXPRESSION | Immunohistochemistry | Multivariate Analysis | ATP-Binding Cassette Sub-Family B Member 2 - immunology | Humans | Middle Aged | Receptors, Androgen - metabolism | Gene Expression Regulation, Neoplastic | Prostatic Neoplasms, Castration-Resistant - immunology | Bone Neoplasms - secondary | Male | RNA, Messenger - metabolism | Case-Control Studies | Prostatic Neoplasms, Castration-Resistant - genetics | Prostatic Neoplasms, Castration-Resistant - pathology | Bone Neoplasms - metabolism | Serine Endopeptidases - genetics | Aged, 80 and over | Bone Neoplasms - genetics | Neoplasm Proteins - genetics | Principal Component Analysis | Prostate-Specific Antigen - genetics | Membrane Proteins - genetics | Oxidoreductases - genetics | Kallikreins - genetics | ATP-Binding Cassette Sub-Family B Member 2 - genetics | Bone Neoplasms - immunology | Hepatocyte Nuclear Factor 3-alpha - genetics | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Prostatic Neoplasms, Castration-Resistant - metabolism | Homeodomain Proteins - genetics | HLA-A Antigens - immunology | Cysteine Endopeptidases - genetics | HLA-A Antigens - genetics | Aged | Cysteine Endopeptidases - immunology | Metastasis | Proteins | Medical research | Histocompatibility antigens | Prostate-specific antigen | Analysis | HLA histocompatibility antigens | Physiological aspects | Medicine, Experimental | Urologi och njurmedicin | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Clinical Medicine | Cancer and Oncology | Urology and Nephrology | Cancer och onkologi
Journal Article
Journal Article
Aging Cell, ISSN 1474-9718, 08/2017, Volume 16, Issue 4, pp. 837 - 846
Summary Kallistatin, an endogenous protein, protects against vascular injury by inhibiting oxidative stress and inflammation in hypertensive rats and enhancing... 
sirtuin 1 | kallistatin | vascular senescence | aging | microRNA‐34a | oxidative stress | microRNA-34a | NECROSIS-FACTOR-ALPHA | TISSUE KALLIKREIN INHIBITOR | BINDING PROTEIN | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | ORGAN INJURY | CAENORHABDITIS-ELEGANS | PROTECTIVE ROLE | PROGENITOR-CELL SENESCENCE | ENDOTHELIAL-CELLS | RENAL INJURY | Sirtuin 1 - metabolism | Diabetes Mellitus, Experimental - drug therapy | Endothelial Progenitor Cells - cytology | MicroRNAs - antagonists & inhibitors | Streptozocin | Humans | Diabetes Mellitus, Experimental - genetics | NADPH Oxidases - metabolism | Caenorhabditis elegans Proteins - metabolism | Cellular Senescence - drug effects | Male | MicroRNAs - metabolism | Sirtuin 1 - genetics | Telomerase - genetics | Plasminogen Activator Inhibitor 1 - metabolism | Superoxides - metabolism | beta-Galactosidase - metabolism | NADPH Oxidases - genetics | Telomerase - metabolism | Diabetes Mellitus, Experimental - chemically induced | Superoxides - antagonists & inhibitors | Nitric Oxide Synthase Type III - metabolism | Plasminogen Activator Inhibitor 1 - genetics | Diabetes Mellitus, Experimental - metabolism | Sirtuins - genetics | Endothelial Progenitor Cells - metabolism | Cellular Senescence - genetics | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Catalase - genetics | Endothelial Progenitor Cells - drug effects | Cells, Cultured | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Nitric Oxide Synthase Type III - genetics | Serpins - pharmacology | Catalase - metabolism | Tumor Necrosis Factor-alpha - pharmacology | Animals | Caenorhabditis elegans - drug effects | Genistein - pharmacology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Mice | MicroRNAs - genetics | beta-Galactosidase - genetics | Caenorhabditis elegans Proteins - genetics | Sirtuins - metabolism | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Gene expression | MicroRNA | Oxidative stress | Senescence | Genistein | INK4a protein | Kinases | NAD(P)H oxidase | Catalase | Rodents | Aging | Aorta | Telomerase | Protein-tyrosine kinase | Tyrosine | Enzymes | Diabetes mellitus | p16 Protein | MiRNA | Superoxide | SIRT1 protein | Life span | Tumor necrosis factor | MicroRNAs | Stem cells | Nematodes | Diabetes | Original
Journal Article
Nature Cell Biology, ISSN 1465-7392, 03/2007, Volume 9, Issue 3, pp. 347 - 353
Posttranslational modifications of histones, such as methylation, regulate chromatin structure and gene expression(1). Recently, lysine-specific demethylase 1... 
TRANSCRIPTION COMPLEX | TRIMETHYLATION | COACTIVATOR | METHYLATION | DOMAIN | PROTEIN | HISTONE H3 | SIGNALS | FHL2 | LYSINE-9 | CELL BIOLOGY | Prostatic Neoplasms - metabolism | RNA, Small Interfering - genetics | Oxidoreductases, N-Demethylating - genetics | Humans | Receptors, Androgen - metabolism | Cercopithecus aethiops | Male | Receptors, Glucocorticoid - metabolism | Receptors, Progesterone - genetics | Tissue Kallikreins - genetics | Neoplasm Proteins - metabolism | Receptors, Progesterone - metabolism | Prostatic Neoplasms - genetics | Transfection | Receptors, Androgen - analysis | Protein Binding - drug effects | Prostate-Specific Antigen - metabolism | Response Elements - genetics | Metribolone - pharmacology | Neoplasm Proteins - genetics | Oxidoreductases, N-Demethylating - metabolism | Prostate-Specific Antigen - genetics | Cell Line | Prostatic Neoplasms - pathology | Transcription Factors - genetics | Gene Expression Regulation - drug effects | Transcription Factors - metabolism | Animals | Histone Demethylases | Receptors, Glucocorticoid - genetics | Cell Line, Tumor | Cell Proliferation - drug effects | MicroRNAs - genetics | HeLa Cells | Histones - metabolism | Jumonji Domain-Containing Histone Demethylases | Evaluation | Hormone receptors | Androgens | Physiological aspects | Histones | Chemical properties | Gene expression | Methylation
Journal Article
Science Translational Medicine, ISSN 1946-6234, 2010, Volume 2, Issue 62, pp. 62ra92 - 62ra92
Journal Article
The Prostate, ISSN 0270-4137, 06/2015, Volume 75, Issue 9, pp. 936 - 946
Background Androgen receptor (AR) is a ligand dependent transcription factor that regulates the transcription of target genes. AR activity is closely involved... 
oxidation | miRNA | androgen receptor | histone demethylation | LSD1 | RECRUITMENT | RECEPTOR | RISK | DAMAGE | REPAIR | INVASION | PROSTATE-CANCER CELLS | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | UROLOGY & NEPHROLOGY | Neoplasms, Hormone-Dependent - metabolism | Prostatic Neoplasms - metabolism | RNA, Small Interfering - genetics | Histone Demethylases - antagonists & inhibitors | DNA, Neoplasm - metabolism | Humans | Receptors, Androgen - metabolism | Male | MicroRNAs - metabolism | Histone Demethylases - genetics | Neoplasms, Hormone-Dependent - genetics | RNA - genetics | Prostatic Neoplasms - genetics | Serine Endopeptidases - genetics | Transcription, Genetic | Prostate-Specific Antigen - metabolism | Prostate-Specific Antigen - genetics | Oxidation-Reduction | Kallikreins - genetics | RNA - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Histone Demethylases - metabolism | Histones - genetics | Receptors, Androgen - genetics | Acetylcysteine - pharmacology | Cell Line, Tumor | Pargyline - pharmacology | Prostatic Neoplasms - enzymology | MicroRNAs - genetics | Serine Endopeptidases - metabolism | DNA, Neoplasm - genetics | Histones - metabolism | RNA, Small Interfering - administration & dosage | Kallikreins - metabolism | Proteins | Monoamine oxidase | MicroRNA | Prostate-specific antigen | DNA | Development and progression | Oxidation-reduction reaction | Genetic transcription | Methylation | Prostate cancer
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2007, Volume 2, Issue 1, pp. 17 - 17
Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of... 
MEDICINE, RESEARCH & EXPERIMENTAL | CHROMOSOME | TAURODONTISM | NOMENCLATURE | CONE-ROD DYSTROPHY | ENAM MUTATIONS | CLASSIFICATION | IDENTIFICATION | LOCUS | NONSENSE MUTATION | AIH1 | Diagnosis, Diff