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Biochemical and Biophysical Research Communications, ISSN 0006-291X, 04/2017, Volume 485, Issue 4, pp. 820 - 825
Ubiquitin-conjugating enzyme E2S (UBE2S), a family of E2 protein in the ubiquitin-proteasome system, is highly expressed in several types of cancers; however,... 
APC/C | Oral squamous cell carcinoma | Ubiquitin-proteasome system | G2/M arrest | P21 | Cell cycle | COMPLEX | E2-EPF UCP | BIOCHEMISTRY & MOLECULAR BIOLOGY | BREAST-CANCER | OVEREXPRESSION | REGULATOR | BIOPHYSICS | ENZYMES | SQUAMOUS-CELL CARCINOMA | CHAINS | PROGRESSION | Immunohistochemistry | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Gene Expression Regulation, Neoplastic | Ubiquitin - metabolism | Male | Mouth Neoplasms - metabolism | Cyclin-Dependent Kinase Inhibitor p21 - genetics | Flow Cytometry | Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome - genetics | RNA Interference | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Female | Mouth Neoplasms - genetics | Cell Proliferation - genetics | Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome - metabolism | Ubiquitin-Conjugating Enzymes - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | G2 Phase Cell Cycle Checkpoints - genetics | Ubiquitin-Conjugating Enzymes - metabolism | Cell Line, Tumor | Mouth Neoplasms - pathology | Aged | Proteasome Endopeptidase Complex - metabolism | Ubiquitin | Medical colleges | Squamous cell carcinoma | Ligases | Analysis | DNA polymerases | Health aspects | Development and progression | MONOCLINIC LATTICES | CHAIN REACTIONS | BIOLOGICAL MARKERS | ANIMAL TISSUES | CELL CYCLE | PHOSPHORUS 21 | 60 APPLIED LIFE SCIENCES | PLANT GROWTH
Journal Article
Oncogene, ISSN 0950-9232, 08/2015, Volume 34, Issue 32, pp. 4229 - 4237
Manganese superoxide dismutase (MnSOD) is a mitochondrially localized primary antioxidant enzyme, known to be essential for the survival of aerobic life and to... 
OXIDATIVE STRESS | LIPID-PEROXIDATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ALPHA | CELL BIOLOGY | OVEREXPRESSION | SKIN CARCINOGENESIS MODEL | EPITHELIAL-CELLS | ONCOLOGY | GLUCOSE | GENETICS & HEREDITY | CANCER METABOLISM | PROTEIN-2 | EXPRESSION | Superoxide Dismutase - genetics | Reactive Oxygen Species - metabolism | TOR Serine-Threonine Kinases - metabolism | Humans | Ion Channels - genetics | Mitochondrial Proteins - genetics | Phosphatidylinositol 3-Kinases - metabolism | TOR Serine-Threonine Kinases - genetics | Mitochondria - genetics | RNA Interference | Mitochondrial Proteins - metabolism | Adenosine Triphosphate - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Cells, Cultured | PPAR alpha - genetics | Superoxide Dismutase - deficiency | Mitochondria - metabolism | Signal Transduction - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Animals | Lactates - metabolism | Ion Channels - metabolism | Glycolysis | Uncoupling Protein 2 | PPAR alpha - metabolism | Uncoupling Protein 1 | Physiological aspects | Superoxide dismutase | Genetic aspects | Mitochondrial diseases | Research | Carcinogenesis | Risk factors | Antioxidants | Enzymes | Signal transduction | Protein expression | Mitochondria | Cancer | Energetic metabolism | UCPs | Redox homeostasis | MnSOD | glycolysis
Journal Article
Journal Article
Clinical Science, ISSN 0143-5221, 03/2011, Volume 120, Issue 5, pp. 195 - 206
Chronic exposure of pancreatic beta-cells to saturated non-esterified fatty acids can lead to inhibition of insulin secretion and apoptosis. Several previous... 
Reactive oxygen species | Type 2 diabetes mellitus | Pancreatic β-cell | Arachidonic acid | Lipotoxicity | Palmitic acid | arachidonic acid | MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | RAT | ISLETS | INSULIN-SECRETION | RELEASE | palmitic acid | INHIBITION | pancreatic beta-cell | FREE FATTY-ACIDS | lipotoxicity | reactive oxygen species | NITRIC-OXIDE | GLUCOSE TOXICITY | CHAIN-LENGTH | Cell Survival - drug effects | Cyclooxygenase 1 - genetics | Cyclooxygenase 1 - biosynthesis | Reactive Oxygen Species - metabolism | Glutathione - metabolism | Humans | Cells, Cultured | Nitrites - metabolism | Cyclooxygenase Inhibitors - pharmacology | Cyclooxygenase 2 - biosynthesis | Gene Expression Regulation - drug effects | Palmitates - antagonists & inhibitors | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Diabetes Mellitus, Type 2 - physiopathology | Insulin-Secreting Cells - drug effects | Cyclooxygenase 2 - genetics | Palmitates - pharmacology | Reverse Transcriptase Polymerase Chain Reaction - methods | Arachidonic Acid - pharmacology | Diabetes Mellitus, Type 2 - pathology | Oxidative Stress - drug effects | Lipoxygenase Inhibitors - pharmacology | Index Medicus | Scd-2, stearoyl-CoA desaturase-2 | Ampk, AMP-activated protein kinase | WT, wild-type | Abcg1, ATP-binding cassette subfamily G member 1 | Gck, glucokinase | pancreatic β-cell | HETE, hydroxyeicosatetraenoic acid | NEFA, non-esterified fatty acid | WST-1, water-soluble tetrazolium salt 1 | RT–PCR (reverse transcription–PCR | NS-398, N-(2-cyclohexyloxyl-4 nitrophenyl)methanesulfonamide | PA, palmitic acid | GSIS, glucose-stimulated insulin secretion | iNOS, inducible NO synthase | TNB, 2-nitro-5-thiobenzoic acid | ROS, reactive oxygen species | Srebp-1c, sterol-regulatory-element-binding protein-1c | T2DM, Type 2 diabetes mellitus | PG, prostaglandin | Ppara, peroxisome-proliferator-activated receptor α | SC-560, 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazole | COX, cyclo-oxygenase | PI, propidium iodide | NF-κB, nuclear factor κB | PLA2, phospholipase A2 | FBS, fetal bovine serum | Ech1, peroxisomal Δ3,5,Δ2,4-dienoyl-CoA isomerase | LT, leukotriene | AA, arachidonic acid | Ppard, peroxisome-proliferator-activated receptor δ | DHE, dihydroethidine | UCP, uncoupling protein
Journal Article
Brain Research, ISSN 0006-8993, 2008, Volume 1228, pp. 81 - 88
Journal Article
Journal Article
FEBS Letters, ISSN 0014-5793, 2001, Volume 491, Issue 1, pp. 154 - 158
Fibrates are hypolipidemic drugs that activate the peroxisome proliferator‐activated receptors. Since fibrates may also increase energy expenditure, we... 
Mitochondrion | Peroxisome | Obesity | Fibrate | Fatty acid | Liver | RT-PCR, reverse transcriptase-polymerase chain reaction | PPAR, peroxisome proliferator-activated receptor | FF, fenofibrate | LPL, lipoprotein lipase | WAT, white adipose tissue | UCP, uncoupling protein | GAPDH, glyceraldehyde 3-phosphate dehydrogenase | ACO, acyl-CoA oxidase | liver | BIOCHEMISTRY & MOLECULAR BIOLOGY | fatty acid | COENZYME-A OXIDASE | peroxisome | ACTIVATED RECEPTOR-ALPHA | FATTY-ACIDS | mitochondrion | CELL BIOLOGY | LIPOPROTEIN METABOLISM | BIOPHYSICS | MESSENGER-RNA | TISSUE DISTRIBUTION | GENE-EXPRESSION | UNCOUPLING PROTEIN-2 | fibrate | PEROXISOME PROLIFERATORS | obesity | Uncoupling Agents - pharmacology | Obesity - drug therapy | Rats, Wistar | Diet - adverse effects | Male | RNA, Messenger - metabolism | Adipose Tissue - metabolism | Fenofibrate - pharmacology | Glyceraldehyde-3-Phosphate Dehydrogenases - pharmacology | Muscles - metabolism | Liver - ultrastructure | Muscles - ultrastructure | Liver - metabolism | Oxygen Consumption | Rats | Mitochondria - metabolism | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | Hypolipidemic Agents - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Peroxisomes - metabolism | Obesity - metabolism | Transcription Factors - metabolism | Animals | Energy Metabolism | Receptors, Cytoplasmic and Nuclear - metabolism
Journal Article
Journal of Molecular Medicine, ISSN 0946-2716, 3/2009, Volume 87, Issue 3, pp. 307 - 320
The ubiquitin proteasome pathway has been implicated in carcinogenesis. However, the role of E2-EPF ubiquitin carrier protein (UCP) in esophageal cancer... 
Human Genetics | Biomedicine | Internal Medicine | Molecular Medicine | E2-EPF ubiquitin carrier protein (UCP) | Response to neoadjuvant CCRT | Membrane array | Epithelial mesenchymal transition | Esophageal cancer | MEDICINE, RESEARCH & EXPERIMENTAL | TGF-BETA | PROTEASOME PATHWAY | HYPOXIA | EPITHELIAL-MESENCHYMAL TRANSITION | IRRADIATION | MOLECULAR MARKERS | COLORECTAL-CANCER | IN-VIVO | GENETICS & HEREDITY | TUMOR-SUPPRESSOR PROTEIN | GROWTH-FACTOR | Predictive Value of Tests | RNA, Small Interfering - genetics | Prognosis | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Humans | Middle Aged | Male | Transfection | Esophageal Neoplasms - metabolism | Reverse Transcriptase Polymerase Chain Reaction - methods | Aged, 80 and over | Adult | Female | Esophageal Neoplasms - therapy | Transforming Growth Factor beta1 - pharmacology | Cell Line | Cell Survival - drug effects | Drug Therapy | Kaplan-Meier Estimate | Carcinoma, Squamous Cell - therapy | Ubiquitin-Conjugating Enzymes - genetics | Combined Modality Therapy | Radiotherapy | Cell Survival - radiation effects | Blotting, Western | Esophageal Neoplasms - genetics | Reverse Transcriptase Polymerase Chain Reaction - instrumentation | Ubiquitin-Conjugating Enzymes - metabolism | Cell Line, Tumor | Aged | Cell Proliferation - drug effects | Cell Proliferation - radiation effects | Immunohistochemistry | Ubiquitin | Usage | Physiological aspects | Development and progression | Genetic aspects | Diagnosis | Research | Risk factors | Index Medicus
Journal Article