Leukemia & Lymphoma, ISSN 1042-8194, 07/2018, Volume 59, Issue 7, pp. 1574 - 1585
Dysregulation of the histone methyltransferase EZH2 plays a critical role in the development of a variety of malignancies including B-cell lymphomas. As a...
EZH2 inhibitors | non-Hodgkin lymphoma | Epigenetic | SELECTIVE-INHIBITION | B-CELL LYMPHOMAS | POLYCOMB | GERMINAL CENTER FORMATION | POTENT | CANCER EPIGENETICS | ONCOLOGY | NON-HODGKIN-LYMPHOMA | HISTONE METHYLTRANSFERASE EZH2 | MUTATIONS | HEMATOLOGY | REPRESSIVE COMPLEX 2 | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Lymphoma, B-Cell - metabolism | Humans | Enzyme Inhibitors - pharmacology | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Drug Resistance, Neoplasm | Treatment Outcome | Antineoplastic Agents - therapeutic use | Clinical Trials as Topic | Combined Modality Therapy | Lymphoma, B-Cell - genetics | Molecular Targeted Therapy | Enzyme Inhibitors - therapeutic use | Animals | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Lymphoma, B-Cell - pathology | Antineoplastic Agents - pharmacology | Epigenesis, Genetic - drug effects | Drug Evaluation, Preclinical | Lymphoma, B-Cell - drug therapy
EZH2 inhibitors | non-Hodgkin lymphoma | Epigenetic | SELECTIVE-INHIBITION | B-CELL LYMPHOMAS | POLYCOMB | GERMINAL CENTER FORMATION | POTENT | CANCER EPIGENETICS | ONCOLOGY | NON-HODGKIN-LYMPHOMA | HISTONE METHYLTRANSFERASE EZH2 | MUTATIONS | HEMATOLOGY | REPRESSIVE COMPLEX 2 | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Lymphoma, B-Cell - metabolism | Humans | Enzyme Inhibitors - pharmacology | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Drug Resistance, Neoplasm | Treatment Outcome | Antineoplastic Agents - therapeutic use | Clinical Trials as Topic | Combined Modality Therapy | Lymphoma, B-Cell - genetics | Molecular Targeted Therapy | Enzyme Inhibitors - therapeutic use | Animals | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Lymphoma, B-Cell - pathology | Antineoplastic Agents - pharmacology | Epigenesis, Genetic - drug effects | Drug Evaluation, Preclinical | Lymphoma, B-Cell - drug therapy
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 6804 - 12
EZH2, a subunit of the polycomb repressive complex 2 (PRC2) catalyzing trimethylation of histone H3 lysine 27 (H3K27), induces epithelial-mesenchymal...
CELLS | METHYLATION | INVASION | PLATELETS | MULTIDISCIPLINARY SCIENCES | HEPATOCYTE GROWTH-FACTOR | GROUP PROTEIN EZH2 | PROLIFERATION | E-CADHERIN | EXPRESSION | TO-MYOFIBROBLAST TRANSDIFFERENTIATION | Cell Line | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Snail Family Transcription Factors - metabolism | Cadherins - metabolism | Vimentin - metabolism | Humans | Cells, Cultured | Endometriosis - pathology | Animals | Snail Family Transcription Factors - genetics | Vimentin - genetics | Endometriosis - metabolism | Epithelial-Mesenchymal Transition | Adult | Female | Mice | Mice, Inbred BALB C | Histones - metabolism | Cadherins - genetics | Polycomb Repressive Complex 2 - metabolism | Vimentin | Transcription factors | Pain perception | Wound healing | Mesenchyme | Epithelial cells | Endometriosis | E-cadherin | Polycomb group proteins | Lysine | Fibrosis | Platelets | Snail protein | Methylation | Cell migration | Endometrium | Histone H3
CELLS | METHYLATION | INVASION | PLATELETS | MULTIDISCIPLINARY SCIENCES | HEPATOCYTE GROWTH-FACTOR | GROUP PROTEIN EZH2 | PROLIFERATION | E-CADHERIN | EXPRESSION | TO-MYOFIBROBLAST TRANSDIFFERENTIATION | Cell Line | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Snail Family Transcription Factors - metabolism | Cadherins - metabolism | Vimentin - metabolism | Humans | Cells, Cultured | Endometriosis - pathology | Animals | Snail Family Transcription Factors - genetics | Vimentin - genetics | Endometriosis - metabolism | Epithelial-Mesenchymal Transition | Adult | Female | Mice | Mice, Inbred BALB C | Histones - metabolism | Cadherins - genetics | Polycomb Repressive Complex 2 - metabolism | Vimentin | Transcription factors | Pain perception | Wound healing | Mesenchyme | Epithelial cells | Endometriosis | E-cadherin | Polycomb group proteins | Lysine | Fibrosis | Platelets | Snail protein | Methylation | Cell migration | Endometrium | Histone H3
Journal Article
BJU International, ISSN 1464-4096, 02/2016, Volume 117, Issue 2, pp. 351 - 362
Objective To investigate the molecular mechanism and clinical significance for an oncogenic role of enhancer of zeste homolog 2 (EZH2) in renal cell carcinoma...
kidney cancer | RCC | DZNep | EMT | survival | EZH2 | DEVELOPMENTAL REGULATORS | METASTASIS | ESTABLISHMENT | POLYCOMB | VIRUS X PROTEIN | HEPATOCELLULAR-CARCINOMA | THERAPY | EMBRYONIC STEM-CELLS | UROLOGY & NEPHROLOGY | EXPRESSION | Immunohistochemistry | Carcinoma, Renal Cell - pathology | Neoplasm Invasiveness | Epigenesis, Genetic | Humans | Gene Expression Regulation, Neoplastic | Polycomb Repressive Complex 2 - drug effects | Cadherins - drug effects | Blotting, Western | Enhancer of Zeste Homolog 2 Protein | Cell Movement - drug effects | Disease-Free Survival | Animals | Heterografts | Chromatin Immunoprecipitation | Cell Line, Tumor | Kidney Neoplasms - pathology | Mice | Carcinoma, Renal Cell - drug therapy | Kidney Neoplasms - drug therapy | Polycomb Repressive Complex 2 - metabolism | Jumonji Domain-Containing Histone Demethylases - metabolism | Real-Time Polymerase Chain Reaction | Epigenetic inheritance | Carcinoma, Renal cell | Analysis
kidney cancer | RCC | DZNep | EMT | survival | EZH2 | DEVELOPMENTAL REGULATORS | METASTASIS | ESTABLISHMENT | POLYCOMB | VIRUS X PROTEIN | HEPATOCELLULAR-CARCINOMA | THERAPY | EMBRYONIC STEM-CELLS | UROLOGY & NEPHROLOGY | EXPRESSION | Immunohistochemistry | Carcinoma, Renal Cell - pathology | Neoplasm Invasiveness | Epigenesis, Genetic | Humans | Gene Expression Regulation, Neoplastic | Polycomb Repressive Complex 2 - drug effects | Cadherins - drug effects | Blotting, Western | Enhancer of Zeste Homolog 2 Protein | Cell Movement - drug effects | Disease-Free Survival | Animals | Heterografts | Chromatin Immunoprecipitation | Cell Line, Tumor | Kidney Neoplasms - pathology | Mice | Carcinoma, Renal Cell - drug therapy | Kidney Neoplasms - drug therapy | Polycomb Repressive Complex 2 - metabolism | Jumonji Domain-Containing Histone Demethylases - metabolism | Real-Time Polymerase Chain Reaction | Epigenetic inheritance | Carcinoma, Renal cell | Analysis
Journal Article
Journal of biological chemistry, ISSN 0021-9258, 08/2018, Volume 293, Issue 33, pp. 12894 - 12907
Epigenetic mechanisms control skeletal development and osteoblast differentiation. Pharmacological inhibition of the histone 3 Lys-27 (H3K27) methyltransferase...
Molecular Biology | Biochemistry | Cell Biology | methyltransferase | OSTEOBLAST DIFFERENTIATION | EPIGENETIC CONTROL | CHROMATIN | enhancer of zeste homolog | BIOCHEMISTRY & MOLECULAR BIOLOGY | bone | osteoblast | osteogenesis | LINEAGE SPECIFICATION | epigenetics | MESENCHYMAL STEM-CELLS | histone methylation | skeleton | OSTEOCALCIN GENE | SKELETAL GROWTH | chromatin regulation | bone development | INTEGRATIVE GENOMICS VIEWER | histone | HISTONE MODIFICATIONS | METHYLTRANSFERASE EZH2 | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Osteogenesis - physiology | Animals | Cell Cycle - physiology | Female | Male | Mice, Transgenic | Mice | Osteoblasts - cytology | Sex Characteristics | Osteoblasts - metabolism
Molecular Biology | Biochemistry | Cell Biology | methyltransferase | OSTEOBLAST DIFFERENTIATION | EPIGENETIC CONTROL | CHROMATIN | enhancer of zeste homolog | BIOCHEMISTRY & MOLECULAR BIOLOGY | bone | osteoblast | osteogenesis | LINEAGE SPECIFICATION | epigenetics | MESENCHYMAL STEM-CELLS | histone methylation | skeleton | OSTEOCALCIN GENE | SKELETAL GROWTH | chromatin regulation | bone development | INTEGRATIVE GENOMICS VIEWER | histone | HISTONE MODIFICATIONS | METHYLTRANSFERASE EZH2 | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Osteogenesis - physiology | Animals | Cell Cycle - physiology | Female | Male | Mice, Transgenic | Mice | Osteoblasts - cytology | Sex Characteristics | Osteoblasts - metabolism
Journal Article
Medical science monitor : international medical journal of experimental and clinical research, ISSN 1643-3750, 10/2018, Volume 24, pp. 7249 - 7255
Background: Brain glioma is a type of common primary intracranial malignant tumor, the prognosis of which is frequently unfavorable. Enhancer of zeste homolog...
MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | Cell Proliferation | PROTEIN EZH2 | PHOSPHORYLATION | POLYCOMB | Cells | BREAST-CANCER | GLIOBLASTOMA | INHIBITION | Glioma | PROSTATE-CANCER | HISTONE METHYLTRANSFERASE EZH2 | RNA, Small Interfering - genetics | Prognosis | Humans | Middle Aged | Brain Neoplasms - pathology | Male | Carcinogenesis | Brain Neoplasms - metabolism | Proto-Oncogene Proteins c-akt - genetics | Proto-Oncogene Proteins c-myc - biosynthesis | Heterografts | Glioblastoma - genetics | Neoplastic Stem Cells - metabolism | Neoplastic Stem Cells - pathology | Adult | Female | Glioblastoma - metabolism | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Cell Proliferation - physiology | Brain Neoplasms - genetics | Proto-Oncogene Proteins c-akt - biosynthesis | Animals | Glioblastoma - pathology | Enhancer of Zeste Homolog 2 Protein - biosynthesis | Mice | Proto-Oncogene Proteins c-myc - genetics
MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | Cell Proliferation | PROTEIN EZH2 | PHOSPHORYLATION | POLYCOMB | Cells | BREAST-CANCER | GLIOBLASTOMA | INHIBITION | Glioma | PROSTATE-CANCER | HISTONE METHYLTRANSFERASE EZH2 | RNA, Small Interfering - genetics | Prognosis | Humans | Middle Aged | Brain Neoplasms - pathology | Male | Carcinogenesis | Brain Neoplasms - metabolism | Proto-Oncogene Proteins c-akt - genetics | Proto-Oncogene Proteins c-myc - biosynthesis | Heterografts | Glioblastoma - genetics | Neoplastic Stem Cells - metabolism | Neoplastic Stem Cells - pathology | Adult | Female | Glioblastoma - metabolism | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Cell Proliferation - physiology | Brain Neoplasms - genetics | Proto-Oncogene Proteins c-akt - biosynthesis | Animals | Glioblastoma - pathology | Enhancer of Zeste Homolog 2 Protein - biosynthesis | Mice | Proto-Oncogene Proteins c-myc - genetics
Journal Article
Cell Death and Disease, ISSN 2041-4889, 10/2010, Volume 1, Issue 10, pp. e85 - e85
There is increasing evidence supporting the role of members of the polycomb group (PcG) gene family in tumor development and progression. However, their...
Nasopharyngeal carcinoma (NPC) | MicroRNA | EZH2 | CELLS | VIRUS | nasopharyngeal carcinoma (NPC) | RADIATION | CELL BIOLOGY | BREAST-CANCER | PATHWAY | GROWTH | GENES | GROUP PROTEINS | microRNA | POLYCOMB REPRESSIVE COMPLEX | EXPRESSION | Nasopharyngeal Carcinoma | Nasopharyngeal Neoplasms - metabolism | Oligonucleotide Array Sequence Analysis | Cell Survival | Down-Regulation | Humans | Computational Biology | MicroRNAs - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Enhancer of Zeste Homolog 2 Protein | DNA-Binding Proteins - metabolism | Transcription Factors - metabolism | Polycomb Repressive Complex 2 | Cell Differentiation | Carcinoma - metabolism | 3' Untranslated Regions | Apoptosis | Original
Nasopharyngeal carcinoma (NPC) | MicroRNA | EZH2 | CELLS | VIRUS | nasopharyngeal carcinoma (NPC) | RADIATION | CELL BIOLOGY | BREAST-CANCER | PATHWAY | GROWTH | GENES | GROUP PROTEINS | microRNA | POLYCOMB REPRESSIVE COMPLEX | EXPRESSION | Nasopharyngeal Carcinoma | Nasopharyngeal Neoplasms - metabolism | Oligonucleotide Array Sequence Analysis | Cell Survival | Down-Regulation | Humans | Computational Biology | MicroRNAs - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Enhancer of Zeste Homolog 2 Protein | DNA-Binding Proteins - metabolism | Transcription Factors - metabolism | Polycomb Repressive Complex 2 | Cell Differentiation | Carcinoma - metabolism | 3' Untranslated Regions | Apoptosis | Original
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2018, Volume 115, Issue 15, pp. E3509 - E3518
Natural killer (NK) cell-mediated tumor cell eradication could inhibit tumor initiation and progression. However, the factors that regulate NK cell-mediated...
HCC | NK cell ligands | NK cells | DNMT3A | EZH2 | ACTIVATION | MULTIDISCIPLINARY SCIENCES | NKG2D RECEPTOR | SORAFENIB | FAMILY | INNATE IMMUNE RECOGNITION | LIGANDS | REJECTION | NIVOLUMAB | EXPRESSION | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Small Molecule Libraries - pharmacology | Humans | Intracellular Signaling Peptides and Proteins - immunology | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA Methylation | Carcinoma, Hepatocellular - drug therapy | NK Cell Lectin-Like Receptor Subfamily K - metabolism | Carcinoma, Hepatocellular - genetics | Killer Cells, Natural - immunology | Liver Neoplasms - pathology | Carcinoma, Hepatocellular - immunology | Intracellular Signaling Peptides and Proteins - genetics | Promoter Regions, Genetic | Enhancer of Zeste Homolog 2 Protein - genetics | GPI-Linked Proteins - immunology | Liver Neoplasms - genetics | Down-Regulation | Liver Neoplasms - drug therapy | Liver Neoplasms - immunology | Hep G2 Cells | Carcinoma, Hepatocellular - pathology | Enhancer of Zeste Homolog 2 Protein - immunology | Cell Line, Tumor | Ligands | GPI-Linked Proteins - genetics | Killer cells | Usage | Care and treatment | Hepatoma | Health aspects | Biological Sciences | PNAS Plus
HCC | NK cell ligands | NK cells | DNMT3A | EZH2 | ACTIVATION | MULTIDISCIPLINARY SCIENCES | NKG2D RECEPTOR | SORAFENIB | FAMILY | INNATE IMMUNE RECOGNITION | LIGANDS | REJECTION | NIVOLUMAB | EXPRESSION | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Small Molecule Libraries - pharmacology | Humans | Intracellular Signaling Peptides and Proteins - immunology | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA Methylation | Carcinoma, Hepatocellular - drug therapy | NK Cell Lectin-Like Receptor Subfamily K - metabolism | Carcinoma, Hepatocellular - genetics | Killer Cells, Natural - immunology | Liver Neoplasms - pathology | Carcinoma, Hepatocellular - immunology | Intracellular Signaling Peptides and Proteins - genetics | Promoter Regions, Genetic | Enhancer of Zeste Homolog 2 Protein - genetics | GPI-Linked Proteins - immunology | Liver Neoplasms - genetics | Down-Regulation | Liver Neoplasms - drug therapy | Liver Neoplasms - immunology | Hep G2 Cells | Carcinoma, Hepatocellular - pathology | Enhancer of Zeste Homolog 2 Protein - immunology | Cell Line, Tumor | Ligands | GPI-Linked Proteins - genetics | Killer cells | Usage | Care and treatment | Hepatoma | Health aspects | Biological Sciences | PNAS Plus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2017, Volume 292, Issue 2, pp. 706 - 722
Regulatory T (Treg) cells expressing the transcription factor FOXP3 play a pivotal role in maintaining immunologic self-tolerance. We and others have shown...
METHYLATION | REPRESSION | PHOSPHORYLATION | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | REGULATORY T-CELLS | GENE-EXPRESSION | DIFFERENTIATION | FOXP3 | PLASTICITY | Forkhead Transcription Factors - immunology | Enhancer of Zeste Homolog 2 Protein - genetics | Humans | Mice, Transgenic | Forkhead Transcription Factors - genetics | Crohn Disease - immunology | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Animals | Crohn Disease - pathology | Enhancer of Zeste Homolog 2 Protein - immunology | Th17 Cells - immunology | Mice | Gene Regulatory Networks - immunology | Cytokines - genetics | Cytokines - immunology | Th17 Cells - pathology | Molecular Bases of Disease | histone methylation | transcriptional corepressor | T helper cells | Crohn's disease | regulatory T cell | inflammatory bowel disease (IBD) | forkhead box P3 (FOXP3) | epigenetics | EZH2
METHYLATION | REPRESSION | PHOSPHORYLATION | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | REGULATORY T-CELLS | GENE-EXPRESSION | DIFFERENTIATION | FOXP3 | PLASTICITY | Forkhead Transcription Factors - immunology | Enhancer of Zeste Homolog 2 Protein - genetics | Humans | Mice, Transgenic | Forkhead Transcription Factors - genetics | Crohn Disease - immunology | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Animals | Crohn Disease - pathology | Enhancer of Zeste Homolog 2 Protein - immunology | Th17 Cells - immunology | Mice | Gene Regulatory Networks - immunology | Cytokines - genetics | Cytokines - immunology | Th17 Cells - pathology | Molecular Bases of Disease | histone methylation | transcriptional corepressor | T helper cells | Crohn's disease | regulatory T cell | inflammatory bowel disease (IBD) | forkhead box P3 (FOXP3) | epigenetics | EZH2
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 09/2016, Volume 59, Issue 18, pp. 8306 - 8325
A new enhancer of zeste homolog 2 (EZH2) inhibitor series comprising a substituted phenyl ring joined to a dimethylpyridone moiety via an amide linkage has...
SELECTIVE-INHIBITION | CHEMISTRY, MEDICINAL | MECHANISM | HISTONE H3 | B-CELL LYMPHOMAS | NON-HODGKIN-LYMPHOMA | MUTATIONS | HYPERTRIMETHYLATION | METHYLTRANSFERASE EZH2 | CANCER | DISCOVERY | Neoplasms - metabolism | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Enhancer of Zeste Homolog 2 Protein - metabolism | Humans | Models, Molecular | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - chemistry | Mice, SCID | Neoplasms - drug therapy | Isoquinolines - chemistry | Animals | Isoquinolines - pharmacology | Cyclization | Drug Design | Lactams - pharmacology | Cell Line, Tumor | Isoquinolines - therapeutic use | Female | Antineoplastic Agents - pharmacology | Mice | Pyridones - therapeutic use | Pyridones - chemistry | Pyridones - pharmacology | Lactams - chemistry
SELECTIVE-INHIBITION | CHEMISTRY, MEDICINAL | MECHANISM | HISTONE H3 | B-CELL LYMPHOMAS | NON-HODGKIN-LYMPHOMA | MUTATIONS | HYPERTRIMETHYLATION | METHYLTRANSFERASE EZH2 | CANCER | DISCOVERY | Neoplasms - metabolism | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Enhancer of Zeste Homolog 2 Protein - metabolism | Humans | Models, Molecular | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - chemistry | Mice, SCID | Neoplasms - drug therapy | Isoquinolines - chemistry | Animals | Isoquinolines - pharmacology | Cyclization | Drug Design | Lactams - pharmacology | Cell Line, Tumor | Isoquinolines - therapeutic use | Female | Antineoplastic Agents - pharmacology | Mice | Pyridones - therapeutic use | Pyridones - chemistry | Pyridones - pharmacology | Lactams - chemistry
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 12/2017, Volume 143, Issue 6, pp. 671 - 683
Elevated expression of enhancer of zeste homolog 2 (EZH2), a histone H3K27 methyltransferase, was observed in gliomas harboring telomerase reverse...
MSI | ATM | TERT | FASN | EZH2 | PENTOSE-PHOSPHATE PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | MISMATCH REPAIR GENE | PROMOTER MUTATIONS | NEUROSCIENCES | COLON-CANCER | STEM-LIKE CELLS | EPITHELIAL-CELLS | PROSTATE-CANCER | IN-VIVO | HUMAN GLIOMAS | FATTY-ACID SYNTHASE | Enhancer of Zeste Homolog 2 Protein - metabolism | Humans | Animals | Heterografts | DNA Damage - physiology | Mice, Nude | Glioblastoma - pathology | Cell Line, Tumor | Glioblastoma - metabolism | Telomerase - metabolism | Mice | Gene Expression Regulation, Neoplastic - physiology | Lipid Metabolism - physiology | Synthesis | DNA damage | Analysis | DNA | Physiological aspects | Development and progression | Genetic engineering | Fatty acids | Glioblastoma multiforme | DNA repair | Telomerase | Phosphorylation | Telomerase reverse transcriptase | RNA-directed DNA polymerase | Brain tumors | Glioblastoma | Methyltransferase | Lipids | Homology | Microsatellite instability | Accumulation | Rodents | Xenografts | Ataxia | Lipid metabolism | Inhibition | Deoxyribonucleic acid--DNA | Microsatellites | Stability | Pharmacology | siRNA | Metabolism | Gene expression | Glioma | Ataxia telangiectasia | Ataxia telangiectasia mutated protein | Mutation | Tumors
MSI | ATM | TERT | FASN | EZH2 | PENTOSE-PHOSPHATE PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | MISMATCH REPAIR GENE | PROMOTER MUTATIONS | NEUROSCIENCES | COLON-CANCER | STEM-LIKE CELLS | EPITHELIAL-CELLS | PROSTATE-CANCER | IN-VIVO | HUMAN GLIOMAS | FATTY-ACID SYNTHASE | Enhancer of Zeste Homolog 2 Protein - metabolism | Humans | Animals | Heterografts | DNA Damage - physiology | Mice, Nude | Glioblastoma - pathology | Cell Line, Tumor | Glioblastoma - metabolism | Telomerase - metabolism | Mice | Gene Expression Regulation, Neoplastic - physiology | Lipid Metabolism - physiology | Synthesis | DNA damage | Analysis | DNA | Physiological aspects | Development and progression | Genetic engineering | Fatty acids | Glioblastoma multiforme | DNA repair | Telomerase | Phosphorylation | Telomerase reverse transcriptase | RNA-directed DNA polymerase | Brain tumors | Glioblastoma | Methyltransferase | Lipids | Homology | Microsatellite instability | Accumulation | Rodents | Xenografts | Ataxia | Lipid metabolism | Inhibition | Deoxyribonucleic acid--DNA | Microsatellites | Stability | Pharmacology | siRNA | Metabolism | Gene expression | Glioma | Ataxia telangiectasia | Ataxia telangiectasia mutated protein | Mutation | Tumors
Journal Article
Journal of Chemical Information and Modeling, ISSN 1549-9596, 08/2017, Volume 57, Issue 8, pp. 2089 - 2098
Combining computational modeling, de novo compound synthesis, and in vitro and cellular assays, we have performed an inhibition study against the enhancer of...
CHEMISTRY, MEDICINAL | COMPUTER SCIENCE, INFORMATION SYSTEMS | ANION TRANSPORT | POLYCOMB | CHEMISTRY, MULTIDISCIPLINARY | CELL-DEATH | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | THERAPEUTIC TARGET | PROSTATE-CANCER | GROUP PROTEIN EZH2 | LYMPHOMA | SIMULATIONS | HISTONE METHYLTRANSFERASE | Càncer | Computational modeling | Enzyme | Enginyeria biomèdica | Enhancer of zeste homolog 2 (EZH2) | Investigació | Research | Enzims | Enzyme activation | Àrees temàtiques de la UPC | Cancer
CHEMISTRY, MEDICINAL | COMPUTER SCIENCE, INFORMATION SYSTEMS | ANION TRANSPORT | POLYCOMB | CHEMISTRY, MULTIDISCIPLINARY | CELL-DEATH | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | THERAPEUTIC TARGET | PROSTATE-CANCER | GROUP PROTEIN EZH2 | LYMPHOMA | SIMULATIONS | HISTONE METHYLTRANSFERASE | Càncer | Computational modeling | Enzyme | Enginyeria biomèdica | Enhancer of zeste homolog 2 (EZH2) | Investigació | Research | Enzims | Enzyme activation | Àrees temàtiques de la UPC | Cancer
Journal Article
Carcinogenesis, ISSN 0143-3334, 11/2015, Volume 36, Issue 11, pp. 1333 - 1340
Enhancer of zeste homolog 2 (EZH2) plays an important role in tumor development and progression by interacting with histone and nonhistone proteins. In the...
GENOMIC INSTABILITY | BREAST EPITHELIAL-CELLS | ANDROGEN RECEPTOR | GENE FUSIONS | ONCOLOGY | TUMOR-CELL PROLIFERATION | POLYCOMB GROUP PROTEIN | EARLY PSA RECURRENCE | HISTONE DEACETYLASE | PROGRESSION | DELETION | Multivariate Analysis | Prostatic Neoplasms - metabolism | Cell Proliferation | Polycomb Repressive Complex 2 - genetics | Prognosis | Tissue Array Analysis | Humans | Middle Aged | Male | Prostate - surgery | Prostate - metabolism | Prostate - pathology | Prostatic Neoplasms - pathology | Gene Expression | Neoplasm Recurrence, Local - metabolism | Neoplasm Recurrence, Local - prevention & control | Prostatic Neoplasms - surgery | Kaplan-Meier Estimate | Postoperative Period | Enhancer of Zeste Homolog 2 Protein | Prostatic Neoplasms - mortality | Disease-Free Survival | Oncogene Proteins, Fusion - genetics | Prostatectomy | Aged | Polycomb Repressive Complex 2 - metabolism | Preoperative Period | Index Medicus
GENOMIC INSTABILITY | BREAST EPITHELIAL-CELLS | ANDROGEN RECEPTOR | GENE FUSIONS | ONCOLOGY | TUMOR-CELL PROLIFERATION | POLYCOMB GROUP PROTEIN | EARLY PSA RECURRENCE | HISTONE DEACETYLASE | PROGRESSION | DELETION | Multivariate Analysis | Prostatic Neoplasms - metabolism | Cell Proliferation | Polycomb Repressive Complex 2 - genetics | Prognosis | Tissue Array Analysis | Humans | Middle Aged | Male | Prostate - surgery | Prostate - metabolism | Prostate - pathology | Prostatic Neoplasms - pathology | Gene Expression | Neoplasm Recurrence, Local - metabolism | Neoplasm Recurrence, Local - prevention & control | Prostatic Neoplasms - surgery | Kaplan-Meier Estimate | Postoperative Period | Enhancer of Zeste Homolog 2 Protein | Prostatic Neoplasms - mortality | Disease-Free Survival | Oncogene Proteins, Fusion - genetics | Prostatectomy | Aged | Polycomb Repressive Complex 2 - metabolism | Preoperative Period | Index Medicus
Journal Article
BMC Cancer, ISSN 1471-2407, 10/2010, Volume 10, Issue 1, pp. 524 - 524
Background: The enhancer of zeste homolog 2 (EZH2) gene exerts oncogene-like activities and its (over) expression has been linked to several human...
PROSTATE | SURVIVAL | ONCOLOGY | MARKER | PREDICT | ENHANCER-OF-ZESTE-HOMOLOG-2 GENE | GROUP PROTEIN EZH2 | DOUBLE-BLIND | PROLIFERATION | IDENTIFICATION | CANCER | Prognosis | Humans | Middle Aged | Risk Factors | Gene Expression Regulation, Neoplastic | Male | Treatment Outcome | Kidney Neoplasms - metabolism | Biomarkers, Tumor | Kidney Neoplasms - diagnosis | Immunohistochemistry - methods | Carcinoma, Renal Cell - metabolism | Neoplasm Metastasis | Carcinoma, Renal Cell - diagnosis | Female | Aged | Gene silencing | Transcription factors | Physiological aspects | Genetic aspects | Carcinoma, Renal cell | Research
PROSTATE | SURVIVAL | ONCOLOGY | MARKER | PREDICT | ENHANCER-OF-ZESTE-HOMOLOG-2 GENE | GROUP PROTEIN EZH2 | DOUBLE-BLIND | PROLIFERATION | IDENTIFICATION | CANCER | Prognosis | Humans | Middle Aged | Risk Factors | Gene Expression Regulation, Neoplastic | Male | Treatment Outcome | Kidney Neoplasms - metabolism | Biomarkers, Tumor | Kidney Neoplasms - diagnosis | Immunohistochemistry - methods | Carcinoma, Renal Cell - metabolism | Neoplasm Metastasis | Carcinoma, Renal Cell - diagnosis | Female | Aged | Gene silencing | Transcription factors | Physiological aspects | Genetic aspects | Carcinoma, Renal cell | Research
Journal Article
Annals of Surgical Oncology, ISSN 1068-9265, 12/2013, Volume 20, Issue S3, pp. 667 - 675
Enhancer of zeste homolog 2 (EZH2) is the catalytic subunit of the polycomb repressive complex 2 (PRC2). When present in PRC2, EZH2 catalyzes trimethylation on...
Oncology | Medicine & Public Health | Surgical Oncology | Surgery | BREAST-CANCER | SURGERY | DEVELOPMENTAL REGULATORS | BILIARY EPITHELIA | ONCOLOGY | EMBRYONIC STEM-CELLS | PROSTATE-CANCER | GROUP PROTEIN EZH2 | PROLIFERATION | POLYCOMB | EXPRESSION | HISTONE METHYLTRANSFERASE | Polycomb Repressive Complex 2 - antagonists & inhibitors | RNA, Small Interfering - genetics | Cell Proliferation | Polycomb Repressive Complex 2 - genetics | Prognosis | Follow-Up Studies | Humans | Male | Cholangiocarcinoma - metabolism | Immunoenzyme Techniques | Bile Ducts, Extrahepatic | Flow Cytometry | Biomarkers, Tumor - metabolism | Bile Ducts, Intrahepatic | Female | Tumor Cells, Cultured | Real-Time Polymerase Chain Reaction | Bile Duct Neoplasms - metabolism | Bile Duct Neoplasms - secondary | RNA, Messenger - genetics | Cholangiocarcinoma - mortality | Survival Rate | Lymphatic Metastasis | Reverse Transcriptase Polymerase Chain Reaction | Disease Progression | Enhancer of Zeste Homolog 2 Protein | Cholangiocarcinoma - pathology | Cell Cycle | Bile Duct Neoplasms - mortality | Aged | Biomarkers, Tumor - genetics | Neoplasm Staging | Polycomb Repressive Complex 2 - metabolism | Apoptosis
Oncology | Medicine & Public Health | Surgical Oncology | Surgery | BREAST-CANCER | SURGERY | DEVELOPMENTAL REGULATORS | BILIARY EPITHELIA | ONCOLOGY | EMBRYONIC STEM-CELLS | PROSTATE-CANCER | GROUP PROTEIN EZH2 | PROLIFERATION | POLYCOMB | EXPRESSION | HISTONE METHYLTRANSFERASE | Polycomb Repressive Complex 2 - antagonists & inhibitors | RNA, Small Interfering - genetics | Cell Proliferation | Polycomb Repressive Complex 2 - genetics | Prognosis | Follow-Up Studies | Humans | Male | Cholangiocarcinoma - metabolism | Immunoenzyme Techniques | Bile Ducts, Extrahepatic | Flow Cytometry | Biomarkers, Tumor - metabolism | Bile Ducts, Intrahepatic | Female | Tumor Cells, Cultured | Real-Time Polymerase Chain Reaction | Bile Duct Neoplasms - metabolism | Bile Duct Neoplasms - secondary | RNA, Messenger - genetics | Cholangiocarcinoma - mortality | Survival Rate | Lymphatic Metastasis | Reverse Transcriptase Polymerase Chain Reaction | Disease Progression | Enhancer of Zeste Homolog 2 Protein | Cholangiocarcinoma - pathology | Cell Cycle | Bile Duct Neoplasms - mortality | Aged | Biomarkers, Tumor - genetics | Neoplasm Staging | Polycomb Repressive Complex 2 - metabolism | Apoptosis
Journal Article