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Nature cell biology, ISSN 1476-4679, 2017, Volume 19, Issue 11, pp. 1358 - 1370
...). PKM2 methylation reversibly shifts the balance of metabolism from oxidative phosphorylation to aerobic glycolysis in breast cancer cells... 
BREAST-CANCER | OXIDATIVE-PHOSPHORYLATION | PROTEIN | TUMOR PROGRESSION | PYRUVATE-KINASE M2 | CA2+ TRANSFER | MITOCHONDRIA | METABOLIC REQUIREMENTS | CELL-PROLIFERATION | ISOFORM | CELL BIOLOGY | Calcium - metabolism | Humans | Endoplasmic Reticulum - metabolism | Carcinogenesis - metabolism | Cell Movement - physiology | Glycolysis - physiology | CARD Signaling Adaptor Proteins - metabolism | MCF-7 Cells | Inositol 1,4,5-Trisphosphate Receptors - metabolism | HEK293 Cells | Female | Membrane Proteins - metabolism | Cell Line | Cell Proliferation - physiology | Oxidative Phosphorylation | Guanylate Cyclase - metabolism | Mitochondria - metabolism | Carcinogenesis - pathology | Animals | Carrier Proteins - metabolism | Mice, Nude | Neoplasm Metastasis - pathology | Thyroid Hormones - metabolism | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Methylation | Cell proliferation | Energy metabolism | Phosphorylation | Calcium | Leukocyte migration | Oxidative metabolism | Pyruvic acid | Kinases | Calcium influx | Metastases | Nanoparticles | Mitochondria | Receptors | Arginine | Tumorigenesis | Inhibition | Inositol 1,4,5-trisphosphate | Inositol 1,4,5-trisphosphate receptors | Cell survival | Pyruvate kinase | Protein arginine methyltransferase | Breast cancer | Metabolism | Calcium (mitochondrial) | Energy balance | Oxidative phosphorylation | Glycolysis | Endoplasmic reticulum | Cell migration | Calcium (reticular) | Cancer
Journal Article
Plant physiology and biochemistry, ISSN 0981-9428, 2017, Volume 110, pp. 167 - 177
Understanding the adverse impact of nanoparticles in crop plants has emerged as one of the most interesting fields of plant research. Therefore, this study has... 
Pea seedlings | Oxidative stress | Anatomical structures | Nitric oxide | Silver nanoparticles | ASSAY | TOXICITY | CHROMIUM | PLANT SCIENCES | RESPONSES | ANTIOXIDANT SYSTEMS | PROTECTIVE ROLE | GROWTH | PLANTS | Nitroprusside - metabolism | Reactive Oxygen Species - metabolism | Glutathione - metabolism | Glutathione Reductase - metabolism | Fluorescence | Nitroprusside - pharmacology | Ascorbic Acid - metabolism | Plant Roots - drug effects | Ascorbate Peroxidases - metabolism | X-Ray Diffraction | Plant Shoots - drug effects | Silver - toxicity | Plant Leaves - drug effects | Plant Proteins - metabolism | Nitric Oxide Donors - pharmacology | Peas - metabolism | Superoxide Dismutase - metabolism | Metal Nanoparticles - ultrastructure | Malondialdehyde - metabolism | Microscopy, Electron, Transmission | Plant Roots - metabolism | Metal Nanoparticles - chemistry | Nitric Oxide Donors - metabolism | Silver - chemistry | Peas - drug effects | Chlorophyll - metabolism | Seedlings - drug effects | Hydrogen Peroxide - metabolism | Chlorophyll - chemistry | Metal Nanoparticles - toxicity | Plant Leaves - metabolism | Photosynthesis - drug effects | Plant Shoots - metabolism | Oxidative Stress - drug effects | Nitric Oxide - metabolism | Seedlings - metabolism | Nanoparticles | Chlorophyll | Silver | Peas | Phytochemistry | Superoxide | Photosynthesis | Nanotechnology
Journal Article
Nature communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, pp. 2270 - 14
.... Starvation, or caloric restriction, is known to activate the transcription factor EB (TFEB), a master regulator of lipid metabolism and lysosomal biogenesis and function... 
LOOP-HELIX PROTEIN | REGULATOR | ACTIVATED PROTEIN-KINASE | LIPID-METABOLISM | MULTIDISCIPLINARY SCIENCES | CALCIUM | CALCINEURIN | RECEPTOR | AUTOPHAGY | ENERGY-METABOLISM | LYSOSOMAL BIOGENESIS | Biguanides - pharmacology | Calcium - metabolism | Caloric Restriction | Longevity - drug effects | Humans | Metabolic Syndrome - metabolism | Autophagy - drug effects | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - agonists | Autophagosomes - drug effects | Lysosomes - metabolism | Liver - drug effects | Diet, High-Fat | Lactams - pharmacology | Lysosomes - drug effects | Starvation | Caenorhabditis elegans - metabolism | Fatty Liver - metabolism | Liver - metabolism | Enzyme Inhibitors - pharmacology | Mitochondria - metabolism | Autophagosomes - metabolism | Mitochondria - drug effects | Digoxin - pharmacology | Animals | Caenorhabditis elegans - drug effects | High-Throughput Screening Assays | Lipid Metabolism - drug effects | Mice | HeLa Cells | Drugs | Animal models | Digoxin | Calcium | Biodegradability | Liver | Disorders | Autophagy | Nanoparticles | Dietary restrictions | Mitochondria | Fatty liver | Biocompatibility | Lipid metabolism | Biodegradation | Lead compounds | Metabolism | Steatosis | Mode of action | Life span | Nematodes | Aging (natural) | Metabolic disorders | Nanotechnology
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2016, Volume 102, pp. 10 - 21
Abstract We recently reported that increased NADPH oxidase 4 (NOX4) expression and activity during aging results in enhanced cellular and mitochondrial... 
Cardiovascular | Nanoparticles | Reactive oxygen species | Inflammation | Cytokines | Atherosclerosis | MITOCHONDRIAL OXIDATIVE STRESS | CARDIAC & CARDIOVASCULAR SYSTEMS | MELITTIN-DERIVED PEPTIDES | TGF-BETA | MONOCYTE CHEMOATTRACTANT PROTEIN-1 | CELL BIOLOGY | GROWTH-FACTOR-BETA | SIRNA TRANSFECTION | SMOOTH-MUSCLE-CELLS | NF-KAPPA-B | TRANSCRIPTIONAL REGULATION | CORONARY-ARTERY-DISEASE | Carotid Arteries - metabolism | RNA, Small Interfering - genetics | Vasculitis - metabolism | Reactive Oxygen Species - metabolism | Muscle, Smooth, Vascular - metabolism | Atherosclerosis - genetics | Humans | Vasculitis - etiology | Vasculitis - pathology | NADPH Oxidases - metabolism | Cell Survival - genetics | Male | NF-kappa B - metabolism | Gene Knockdown Techniques | Aging - genetics | RNA Interference | Inflammation Mediators - metabolism | NADPH Oxidases - genetics | Cytokines - genetics | Myocytes, Smooth Muscle - metabolism | Disease Models, Animal | Atherosclerosis - pathology | Cytokines - metabolism | MAP Kinase Kinase Kinases - metabolism | Mitochondria - metabolism | NADPH Oxidase 4 | Atherosclerosis - metabolism | Hydrogen Peroxide - metabolism | Mice, Knockout | Animals | Biomarkers | Carotid Arteries - pathology | Mice | Aging - metabolism | Oxidases | RNA | Genes | Transforming growth factors | Gene expression | Medical colleges | Anopheles | Peptides | Peroxides | Index Medicus
Journal Article
Scientific reports, ISSN 2045-2322, 2015, Volume 5, Issue 1, p. 11618
Journal Article
Molecular therapy, ISSN 1525-0016, 2017, Volume 25, Issue 7, pp. 1718 - 1729
Inhibition of Notch signaling via systemic drug administration triggers conversion of white adipocytes into beige adipocytes (browning) and reduces adiposity.... 
PLGA | Notch signaling | adipocyte | browning | adipose tissue | nanoparticle | Notch inhibitor | drug delivery | obesity | dibenzazepine | DRUG | MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATION | CONVERSION | NOTCH | MECHANISMS | PREVALENCE | INHIBITION | TEMPERATURE | FAT-CELLS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | PROMOTES | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - agonists | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | Nanoparticles - chemistry | Obesity - drug therapy | Adipose Tissue, White - metabolism | Male | Obesity - genetics | Drug Carriers | Cell Cycle Proteins - antagonists & inhibitors | Dibenzazepines - pharmacology | Basic Helix-Loop-Helix Transcription Factors - metabolism | Nanoparticles - metabolism | Iodide Peroxidase - metabolism | Apoptosis Regulatory Proteins - genetics | Cell Cycle Proteins - genetics | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism | Polyglycolic Acid - metabolism | Energy Metabolism - genetics | Adipose Tissue, White - pathology | Basic Helix-Loop-Helix Transcription Factors - genetics | Lactic Acid - chemistry | Signal Transduction | Lactic Acid - metabolism | Mice, Inbred C57BL | Transcription Factor HES-1 - metabolism | Cell Cycle Proteins - metabolism | Gene Expression Regulation | Basic Helix-Loop-Helix Transcription Factors - antagonists & inhibitors | Adipose Tissue, Brown - pathology | Apoptosis Regulatory Proteins - metabolism | Obesity - metabolism | Obesity - pathology | Anti-Obesity Agents - chemistry | Animals | Transcription Factor HES-1 - antagonists & inhibitors | Transcription Factor HES-1 - genetics | Polyglycolic Acid - chemistry | Apoptosis Regulatory Proteins - agonists | Dibenzazepines - chemistry | Mice, Obese | Adipose Tissue, Brown - drug effects | Adipose Tissue, Brown - metabolism | Mice | Iodide Peroxidase - genetics | Anti-Obesity Agents - pharmacology | Adipose Tissue, White - drug effects | Energy Metabolism - drug effects | Obesity | Immunoglobulins | Adipose tissue | Homeostasis | Adipocytes | Gene expression | Metabolism | Nanoparticles | Proteins | Microscopy | Internalization | Poly(lactide-co-glycolide) | Biotechnology industry | Metabolic disorders | Original
Journal Article
Fertility and sterility, ISSN 0015-0282, 2015, Volume 104, Issue 6, pp. 1552 - 1560.e3
Objective To investigate the engraftment and proliferation of superparamagnetic iron oxide nanoparticles (SPIOs)-labeled human CD133+ bone marrow-derived stem... 
Internal Medicine | Obstetrics and Gynecology | Asherman syndrome | bone marrow-derived stem cells (BMDSCs) | CD133+cells | superparamagnetic iron oxide nanoparticles (SPIOs) | cells | CD133 | POPULATION | MOBILIZATION | REGENERATION | PHENOTYPE | MOUSE ENDOMETRIUM | CD133(+) cells | IDENTIFICATION | RAT MODEL | OBSTETRICS & GYNECOLOGY | REPRODUCTIVE BIOLOGY | THIN ENDOMETRIUM | DISEASE | DIFFERENTIATION | Cell Proliferation | Prospective Studies | Humans | Middle Aged | Cell Tracking - methods | Glycoproteins - metabolism | Ki-67 Antigen - metabolism | Insulin-Like Growth Factor I - genetics | Gynatresia - physiopathology | Stem Cells - metabolism | Gynatresia - genetics | Antigens, CD - metabolism | Atrophy | Stem Cell Transplantation | Peptides - metabolism | Thrombospondin 1 - genetics | Bone Marrow Transplantation | Adult | Female | Disease Models, Animal | Endometrium - metabolism | Biomarkers - metabolism | Gynatresia - surgery | Paracrine Communication | Cell Survival | Glycosaminoglycans - metabolism | Gene Expression Regulation | Graft Survival | Clinical Trials as Topic | Mice, SCID | AC133 Antigen | Collagen - metabolism | Animals | Gynatresia - metabolism | Endometrium - physiopathology | Mice, Inbred NOD | Mice | Thrombospondin 1 - metabolism | Endometrium - pathology | Gynatresia - pathology | Bone Marrow Cells - metabolism | Insulin-Like Growth Factor I - metabolism
Journal Article
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 48, pp. 17104 - 17109
Metastasis portends a poor prognosis for cancer patients. Primary tumor cells disseminate through the bloodstream before the appearance of detectable... 
Vimentin | Epithelial cells | Blood cells | Cell lines | Stem cells | Fluorescence | Breast cancer | Blood | Tumors | Cancer | Diagnostic | Cancer metastasis | MRNA | Nanotechnology | NanoFlares | nanotechnology | mRNA | diagnostic | cancer metastasis | SURVIVAL | MECHANISM | MULTIDISCIPLINARY SCIENCES | PERIPHERAL-BLOOD | EPITHELIAL-MESENCHYMAL TRANSITION | REGULATOR | PREDICT | METASTATIC BREAST-CANCER | PROGRESSION | MESSENGER-RNA DETECTION | Carbocyanines - chemistry | Cadherins - metabolism | Vimentin - metabolism | Humans | Neoplastic Cells, Circulating - metabolism | Carbocyanines - metabolism | Transplantation, Heterologous | Green Fluorescent Proteins - genetics | RNA, Messenger - metabolism | DNA, Antisense - genetics | Breast Neoplasms - metabolism | Vimentin - genetics | Base Sequence | Biomarkers, Tumor - metabolism | Female | Cadherins - genetics | Gold - chemistry | Green Fluorescent Proteins - metabolism | Nanotechnology - methods | Metal Nanoparticles - chemistry | RNA, Messenger - genetics | Neoplastic Cells, Circulating - chemistry | DNA, Antisense - metabolism | Fibronectins - metabolism | Breast Neoplasms - genetics | Breast Neoplasms - blood | Cell Line, Tumor | Luminescent Proteins - genetics | Biomarkers, Tumor - genetics | Fibronectins - genetics | DNA, Antisense - chemistry | Microscopy, Fluorescence | Luminescent Proteins - metabolism | Health aspects | Identification and classification | Cancer cells | Biological Sciences
Journal Article
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 1882 - 11
Journal Article
International journal of molecular sciences, ISSN 1422-0067, 2018, Volume 20, Issue 1, p. 95
.... in order to meet the high requirement of iron, neoplastic cells have remodeled iron metabolism pathways, including acquisition, storage, and efflux, which makes manipulating iron homeostasis... 
Iron homeostasis | Iron manipulating strategies | Epigenetic regulation | Tumor microenvironment | Cancer | iron manipulating strategies | iron homeostasis | BIOCHEMISTRY & MOLECULAR BIOLOGY | GELATINASE-ASSOCIATED LIPOCALIN | MAGNETIC NANOPARTICLES | epigenetic regulation | CHEMISTRY, MULTIDISCIPLINARY | EPITHELIAL-MESENCHYMAL TRANSITION | BREAST-CANCER | HEPATOCELLULAR-CARCINOMA | OXIDE NANOPARTICLES | TRANSFERRIN RECEPTOR 1 | PHOTOTHERMAL THERAPY | cancer | CELL-CYCLE | tumor microenvironment | REGULATORY PROTEIN-1 | Neoplasms - metabolism | Iron Chelating Agents - therapeutic use | Neoplasm Metastasis | Epigenomics | Reactive Oxygen Species - metabolism | Humans | Tumor Microenvironment | Lipid Peroxidation | Neoplasms - pathology | Iron - metabolism | Neoplasms - drug therapy | Ascorbic acid | Homeostasis | Iron | Genomes | Biosynthesis | Metastasis | Cancer therapies | Genetic screening | Ovarian cancer | Anticancer properties | Proteins | Angiogenesis | Demethylation | Heterochromatin | Cell growth | Epidermal growth factor | Enzymatic activity | Cell cycle | DNA methylation | Physiology | Sulfur | Growth factors | Deoxyribonucleic acid--DNA | Enzymes | Epidermal growth factor receptors | Therapeutic applications | Non-small cell lung carcinoma | Breast cancer | Lung carcinoma | Metabolism | Depletion | Epigenetics | Ketoglutaric acid | Chelating agents | Prostate cancer
Journal Article