Current Molecular Medicine, ISSN 1566-5240, 2010, Volume 10, Issue 5, pp. 454 - 466
One of the most intriguing enzymes of sphingolipid biology is acid sphingomyelinase (ASMase). In a phospholipase C reaction, ASMase catalyzes the cleavage of...
Membranes and sphingolipid | Ceramide | Protein kinase c | Sphingomyelinase | Apoptosis | Cancer | MEDICINE, RESEARCH & EXPERIMENTAL | DELTA-MEDIATED PHOSPHORYLATION | STRESS-INDUCED APOPTOSIS | apoptosis | NECROSIS-FACTOR-ALPHA | TRICYCLIC ANTI-DEPRESSANTS | CERAMIDE GENERATION | membranes and sphingolipids | DEFICIENT MOUSE MODEL | CELL-DEATH | NIEMANN-PICK-DISEASE | sphingomyelinase | cancer | CYSTIC-FIBROSIS | NF-KAPPA-B | protein kinase C
Membranes and sphingolipid | Ceramide | Protein kinase c | Sphingomyelinase | Apoptosis | Cancer | MEDICINE, RESEARCH & EXPERIMENTAL | DELTA-MEDIATED PHOSPHORYLATION | STRESS-INDUCED APOPTOSIS | apoptosis | NECROSIS-FACTOR-ALPHA | TRICYCLIC ANTI-DEPRESSANTS | CERAMIDE GENERATION | membranes and sphingolipids | DEFICIENT MOUSE MODEL | CELL-DEATH | NIEMANN-PICK-DISEASE | sphingomyelinase | cancer | CYSTIC-FIBROSIS | NF-KAPPA-B | protein kinase C
Journal Article
Biochemical Society Transactions, ISSN 0300-5127, 11/2005, Volume 33, Issue 5, pp. 1166 - 1169
Journal Article
Biochemistry and Cell Biology, ISSN 0829-8211, 02/2004, Volume 82, Issue 1, pp. 27 - 44
Ceramide, an emerging bioactive lipid and second messenger, is mainly generated by hydrolysis of sphingomyelin through the action of sphingomyelinases. At...
Niemann-Pick disease | Ceramide | FAN (factor associated with N-Smase activation) | Sphingomyelinase | Apoptosis | PROTEIN-KINASE-C | CERAMIDE-INDUCED APOPTOSIS | FAN (factor associated with N-SMase activation) | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | LOW-DENSITY-LIPOPROTEIN | apoptosis | TRICYCLIC ANTI-DEPRESSANTS | COMPLETE NUCLEOTIDE-SEQUENCE | NERVE GROWTH-FACTOR | CELL BIOLOGY | ceramide | TUMOR-NECROSIS-FACTOR | sphingomyelinase | RETINOBLASTOMA GENE-PRODUCT | MAGNESIUM-DEPENDENT SPHINGOMYELINASE | Ions - chemistry | Sphingomyelins - metabolism | Humans | Enzyme Inhibitors - pharmacology | Ceramides - biosynthesis | Hydrolysis | Magnesium - chemistry | Animals | Proteins - metabolism | Sphingomyelin Phosphodiesterase - antagonists & inhibitors | Sphingomyelin Phosphodiesterase - metabolism | Second Messenger Systems - physiology | HeLa Cells | Ceramides - physiology | Hydrogen-Ion Concentration
Niemann-Pick disease | Ceramide | FAN (factor associated with N-Smase activation) | Sphingomyelinase | Apoptosis | PROTEIN-KINASE-C | CERAMIDE-INDUCED APOPTOSIS | FAN (factor associated with N-SMase activation) | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | LOW-DENSITY-LIPOPROTEIN | apoptosis | TRICYCLIC ANTI-DEPRESSANTS | COMPLETE NUCLEOTIDE-SEQUENCE | NERVE GROWTH-FACTOR | CELL BIOLOGY | ceramide | TUMOR-NECROSIS-FACTOR | sphingomyelinase | RETINOBLASTOMA GENE-PRODUCT | MAGNESIUM-DEPENDENT SPHINGOMYELINASE | Ions - chemistry | Sphingomyelins - metabolism | Humans | Enzyme Inhibitors - pharmacology | Ceramides - biosynthesis | Hydrolysis | Magnesium - chemistry | Animals | Proteins - metabolism | Sphingomyelin Phosphodiesterase - antagonists & inhibitors | Sphingomyelin Phosphodiesterase - metabolism | Second Messenger Systems - physiology | HeLa Cells | Ceramides - physiology | Hydrogen-Ion Concentration
Journal Article
Biochemistry, ISSN 0006-2960, 04/2001, Volume 40, Issue 16, pp. 4893 - 4903
Many enzymes of sphingolipid metabolism are regulated in response to extra- and intracellular stimuli and in turn serve as regulators of levels of bioactive...
ACTIVATED PROTEIN-KINASE | P55 TNF-RECEPTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | INDUCED SPHINGOMYELIN HYDROLYSIS | LOW-DENSITY-LIPOPROTEIN | NECROSIS-FACTOR-ALPHA | HUMAN ACID SPHINGOMYELINASE | VEIN ENDOTHELIAL-CELLS | FULL-LENGTH CDNA | SMOOTH-MUSCLE CELLS | C-FOS EXPRESSION | Eukaryotic Cells - enzymology | Sphingolipids - chemistry | Eukaryotic Cells - chemistry | Acyltransferases - physiology | Saccharomyces cerevisiae - physiology | Signal Transduction | Humans | Sphingolipids - metabolism | Eukaryotic Cells - physiology | Phosphoric Diester Hydrolases - physiology | Saccharomyces cerevisiae - chemistry | Serine C-Palmitoyltransferase | Animals | Saccharomyces cerevisiae - enzymology | Sphingomyelin Phosphodiesterase - physiology | Sphingolipids | Lipid metabolism | Research
ACTIVATED PROTEIN-KINASE | P55 TNF-RECEPTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | INDUCED SPHINGOMYELIN HYDROLYSIS | LOW-DENSITY-LIPOPROTEIN | NECROSIS-FACTOR-ALPHA | HUMAN ACID SPHINGOMYELINASE | VEIN ENDOTHELIAL-CELLS | FULL-LENGTH CDNA | SMOOTH-MUSCLE CELLS | C-FOS EXPRESSION | Eukaryotic Cells - enzymology | Sphingolipids - chemistry | Eukaryotic Cells - chemistry | Acyltransferases - physiology | Saccharomyces cerevisiae - physiology | Signal Transduction | Humans | Sphingolipids - metabolism | Eukaryotic Cells - physiology | Phosphoric Diester Hydrolases - physiology | Saccharomyces cerevisiae - chemistry | Serine C-Palmitoyltransferase | Animals | Saccharomyces cerevisiae - enzymology | Sphingomyelin Phosphodiesterase - physiology | Sphingolipids | Lipid metabolism | Research
Journal Article
Oncogene, ISSN 0950-9232, 11/2017, Volume 36, Issue 47, pp. 6649 - 6657
The protein p38 mitogen-activated protein kinase (MAPK) delta isoform (p38 delta) is a poorly studied member of the MAPK family. Data analysis from The Cancer...
LOCALIZATION | ACTIVATED PROTEIN-KINASE | P38-GAMMA | P38-DELTA | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | INVASION | ONCOLOGY | EPITHELIAL-SPECIFIC DISRUPTION | GROWTH | GENETICS & HEREDITY | TRANSGENIC MOUSE MODEL | EXPRESSION | TUMORIGENESIS | Cell Proliferation | Tissue Array Analysis | Humans | Mice, Transgenic | Cell Adhesion | Disease Progression | Mammary Neoplasms, Experimental - genetics | Animals | Protein Isoforms - metabolism | Lung Neoplasms - secondary | MCF-7 Cells | Breast Neoplasms - pathology | Mammary Neoplasms, Experimental - pathology | Mitogen-Activated Protein Kinase 13 - metabolism | Female | Mice | Mitogen-Activated Protein Kinase 13 - genetics | Breast - pathology | Protein Isoforms - genetics | Care and treatment | Development and progression | Breast cancer | Genetic aspects | Gene expression | Tumor proteins | Protein kinases | Health aspects | Cell proliferation | Lung cancer | Data processing | MAP kinase | Genomes | Metastasis | Kinases | Cell adhesion & migration | Metastases | Proteins | Cell growth | Protein kinase | Cell lines | Cell adhesion | Focal adhesion kinase | Tumors | p-FAK Ty397 | metastasis | MMTV-PyMT | Stat3 | breast cancer | p38δ | MAPK
LOCALIZATION | ACTIVATED PROTEIN-KINASE | P38-GAMMA | P38-DELTA | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | INVASION | ONCOLOGY | EPITHELIAL-SPECIFIC DISRUPTION | GROWTH | GENETICS & HEREDITY | TRANSGENIC MOUSE MODEL | EXPRESSION | TUMORIGENESIS | Cell Proliferation | Tissue Array Analysis | Humans | Mice, Transgenic | Cell Adhesion | Disease Progression | Mammary Neoplasms, Experimental - genetics | Animals | Protein Isoforms - metabolism | Lung Neoplasms - secondary | MCF-7 Cells | Breast Neoplasms - pathology | Mammary Neoplasms, Experimental - pathology | Mitogen-Activated Protein Kinase 13 - metabolism | Female | Mice | Mitogen-Activated Protein Kinase 13 - genetics | Breast - pathology | Protein Isoforms - genetics | Care and treatment | Development and progression | Breast cancer | Genetic aspects | Gene expression | Tumor proteins | Protein kinases | Health aspects | Cell proliferation | Lung cancer | Data processing | MAP kinase | Genomes | Metastasis | Kinases | Cell adhesion & migration | Metastases | Proteins | Cell growth | Protein kinase | Cell lines | Cell adhesion | Focal adhesion kinase | Tumors | p-FAK Ty397 | metastasis | MMTV-PyMT | Stat3 | breast cancer | p38δ | MAPK
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 1994, Volume 269, Issue 5, pp. 3125 - 3128
LEUKEMIA HL-60 CELLS | PROTEIN-KINASE-C | BIOCHEMISTRY & MOLECULAR BIOLOGY | SERINE PALMITOYLTRANSFERASE | SPHINGOSINE | NECROSIS-FACTOR-ALPHA | FACTOR RECEPTOR PHOSPHORYLATION | DIFFERENTIATION | SIGNAL TRANSDUCTION | SACCHAROMYCES-CEREVISIAE | EPIDERMOID CARCINOMA-CELLS | Cell Line | Receptor, Epidermal Growth Factor - metabolism | Animals | Ceramides - metabolism | Sphingomyelins - metabolism | Signal Transduction | Models, Biological | Humans | Genes, myc | Second Messenger Systems
Journal Article
Oncogene, ISSN 0950-9232, 05/2016, Volume 35, Issue 21, pp. 2801 - 2812
Targeting cell motility, which is required for dissemination and metastasis, has therapeutic potential for ovarian cancer metastasis, and regulatory mechanisms...
ACTIVATED PROTEIN-KINASE | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | C2 DOMAIN | ARACHIDONIC-ACID | LIPOSOMAL DELIVERY | FACTOR RECEPTOR | OKADAIC ACID | CELL BIOLOGY | EPITHELIAL-CELLS | ONCOLOGY | SHORT-CHAIN CERAMIDE | EPIDERMAL-GROWTH-FACTOR | GENETICS & HEREDITY | Cell Movement - drug effects | Animals | Humans | Ovarian Neoplasms - pathology | Cell Line, Tumor | Female | Cell Proliferation - drug effects | Mice | Ovarian Neoplasms - drug therapy | Phosphatidylinositol 3-Kinase - metabolism | Ceramides - pharmacology | Ovarian Neoplasms - enzymology | cell motility | ceramide | metastasis and dissemination | phosphoinositide 3-kinase C2β | ovarian cancer
ACTIVATED PROTEIN-KINASE | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | C2 DOMAIN | ARACHIDONIC-ACID | LIPOSOMAL DELIVERY | FACTOR RECEPTOR | OKADAIC ACID | CELL BIOLOGY | EPITHELIAL-CELLS | ONCOLOGY | SHORT-CHAIN CERAMIDE | EPIDERMAL-GROWTH-FACTOR | GENETICS & HEREDITY | Cell Movement - drug effects | Animals | Humans | Ovarian Neoplasms - pathology | Cell Line, Tumor | Female | Cell Proliferation - drug effects | Mice | Ovarian Neoplasms - drug therapy | Phosphatidylinositol 3-Kinase - metabolism | Ceramides - pharmacology | Ovarian Neoplasms - enzymology | cell motility | ceramide | metastasis and dissemination | phosphoinositide 3-kinase C2β | ovarian cancer
Journal Article
BBA - Molecular and Cell Biology of Lipids, ISSN 1388-1981, 2006, Volume 1761, Issue 8, pp. 927 - 946
Emerging information on sphingolipid metabolism and signaling is leading to a better understanding of cellular processes such as apoptosis, cancer, cell...
Ceramide 1-phosphate | Glycosphingolipid | Sphingosine | Ceramide | Sphingolipid | CERT | Sphingomyelinase | Sphingosine 1-phosphate | CYTOSOLIC PHOSPHOLIPASE A | sphingolipid | BIOCHEMISTRY & MOLECULAR BIOLOGY | X-RAY-STRUCTURE | glycosphingolipid | ACID-BETA-GLUCOSIDASE | sphingosine | SITE-DIRECTED MUTAGENESIS | CELL BIOLOGY | ceramide | PHOSPHATIDYLCHOLINE-TRANSFER PROTEIN | DENSITY-LIPOPROTEIN PARTICLES | BIOPHYSICS | BACILLUS-CEREUS SPHINGOMYELINASE | GLYCOLIPID TRANSFER PROTEIN | sphingomyelinase | PLECKSTRIN HOMOLOGY DOMAIN | ceramide 1-phosphate | SURFACE-PLASMON RESONANCE | sphingosine 1-phosphate | Physiological aspects | Enzymes | Sphingolipids | Plant lipids
Ceramide 1-phosphate | Glycosphingolipid | Sphingosine | Ceramide | Sphingolipid | CERT | Sphingomyelinase | Sphingosine 1-phosphate | CYTOSOLIC PHOSPHOLIPASE A | sphingolipid | BIOCHEMISTRY & MOLECULAR BIOLOGY | X-RAY-STRUCTURE | glycosphingolipid | ACID-BETA-GLUCOSIDASE | sphingosine | SITE-DIRECTED MUTAGENESIS | CELL BIOLOGY | ceramide | PHOSPHATIDYLCHOLINE-TRANSFER PROTEIN | DENSITY-LIPOPROTEIN PARTICLES | BIOPHYSICS | BACILLUS-CEREUS SPHINGOMYELINASE | GLYCOLIPID TRANSFER PROTEIN | sphingomyelinase | PLECKSTRIN HOMOLOGY DOMAIN | ceramide 1-phosphate | SURFACE-PLASMON RESONANCE | sphingosine 1-phosphate | Physiological aspects | Enzymes | Sphingolipids | Plant lipids
Journal Article
Trends in Biochemical Sciences, ISSN 0968-0004, 1999, Volume 24, Issue 6, pp. 224 - 225
Ceramide | Diglyceride kinase assay | Apoptosis | PROGRAMMED CELL-DEATH | MEMBRANE-FUSION | FAS-INDUCED APOPTOSIS | ACTIVATION | ACID SPHINGOMYELINASE GENE | INHIBITION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENDOTHELIAL-CELLS | GENERATION | SECRETORY SPHINGOMYELINASE | SACCHAROMYCES-CEREVISIAE | Ceramides - agonists | Animals | Ceramides - physiology | Humans | Stress, Physiological | Sphingolipids | Cellular signal transduction | Research | Saccharomyces | Cell death
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 05/2016, Volume 136, Issue 5, pp. S78 - S78
Journal Article
Oncogene, ISSN 0950-9232, 03/2012, Volume 31, Issue 9, pp. 1166 - 1175
p53 is a crucial tumor suppressor that is mutated or deleted in a majority of cancers. Exactly how p53 prevents tumor progression has proved elusive for many...
senescence | ceramide | cancer | sphingosine-1-phosphate | sphingosine kinase | p53 | CERAMIDE-INDUCED APOPTOSIS | GENOTOXIC STRESS | MICE DEFICIENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOWN-REGULATION | CYCLE ARREST | HIGH EXPRESSION | TANDEM MASS-SPECTROMETRY | QUANTITATIVE-ANALYSIS | CELL BIOLOGY | PROGRAMMED CELL-DEATH | ONCOLOGY | GENETICS & HEREDITY | BIOACTIVE SPHINGOLIPIDS | Neoplasms - metabolism | Cell Line | Cellular Senescence - genetics | Mice, Inbred C57BL | Tumor Suppressor Protein p53 - metabolism | Neoplasms - mortality | Male | Phosphotransferases (Alcohol Group Acceptor) - genetics | Cell Transformation, Neoplastic - metabolism | Tumor Suppressor Protein p53 - genetics | Mice, Knockout | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Animals | Neoplasms - genetics | Cell Transformation, Neoplastic - genetics | Tumor Burden - genetics | Mice | Enzyme Activation - genetics | Sphingosine | Physiological aspects | Research | Tumor proteins | Phosphotransferases | Risk factors | Tumors | Signal transduction | Lipids | Kinases | Gene expression | Cell cycle | Cancer | Enzymes | Senescence | Tumor cells | Genotoxicity | Heterozygotes | Homeostasis | Recovery of function | sphingolipid ceramide | Sphingolipids | Lymphoma | p53 protein | Sphingosine 1-phosphate | Thymus | Life span | Ceramide | Tumor suppressor genes | Apoptosis
senescence | ceramide | cancer | sphingosine-1-phosphate | sphingosine kinase | p53 | CERAMIDE-INDUCED APOPTOSIS | GENOTOXIC STRESS | MICE DEFICIENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOWN-REGULATION | CYCLE ARREST | HIGH EXPRESSION | TANDEM MASS-SPECTROMETRY | QUANTITATIVE-ANALYSIS | CELL BIOLOGY | PROGRAMMED CELL-DEATH | ONCOLOGY | GENETICS & HEREDITY | BIOACTIVE SPHINGOLIPIDS | Neoplasms - metabolism | Cell Line | Cellular Senescence - genetics | Mice, Inbred C57BL | Tumor Suppressor Protein p53 - metabolism | Neoplasms - mortality | Male | Phosphotransferases (Alcohol Group Acceptor) - genetics | Cell Transformation, Neoplastic - metabolism | Tumor Suppressor Protein p53 - genetics | Mice, Knockout | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Animals | Neoplasms - genetics | Cell Transformation, Neoplastic - genetics | Tumor Burden - genetics | Mice | Enzyme Activation - genetics | Sphingosine | Physiological aspects | Research | Tumor proteins | Phosphotransferases | Risk factors | Tumors | Signal transduction | Lipids | Kinases | Gene expression | Cell cycle | Cancer | Enzymes | Senescence | Tumor cells | Genotoxicity | Heterozygotes | Homeostasis | Recovery of function | sphingolipid ceramide | Sphingolipids | Lymphoma | p53 protein | Sphingosine 1-phosphate | Thymus | Life span | Ceramide | Tumor suppressor genes | Apoptosis
Journal Article
Cell death & disease, ISSN 2041-4889, 03/2016, Volume 7, Issue 3, pp. e2124 - e2124
Increasing studies suggest that ceramides differing in acyl chain length and/or degree of unsaturation have distinct roles in mediating biological responses....
SPHINGOLIPID METABOLISM | INCREASES INFLAMMATION | DEXTRAN SULFATE | ULCERATIVE-COLITIS | GENE-EXPRESSION | SODIUM-INDUCED COLITIS | CYSTIC-FIBROSIS | INFLAMMATORY BOWEL DISEASES | SPHINGOSINE KINASE | INTESTINAL EPITHELIAL-CELLS | CELL BIOLOGY | Leukocytes, Mononuclear - metabolism | Substrate Specificity | Colitis - pathology | Male | Leukocytes, Mononuclear - immunology | Female | Disease Models, Animal | Ceramides - metabolism | Lipopolysaccharides - toxicity | Cytokines - metabolism | Immunity, Innate - drug effects | Colon - pathology | Mice, Inbred C57BL | Ceramides - analysis | Alkaline Ceramidase - genetics | Colon - metabolism | Dextran Sulfate - toxicity | Mice, Knockout | Alkaline Ceramidase - deficiency | Up-Regulation - drug effects | Colitis - etiology | Animals | Cell Transformation, Neoplastic | Colitis - metabolism | Leukocytes, Mononuclear - cytology | Mice | Inflammatory bowel disease | Enzymes | Tumorigenesis | Cellular biology | Rodents | Immune system | Original
SPHINGOLIPID METABOLISM | INCREASES INFLAMMATION | DEXTRAN SULFATE | ULCERATIVE-COLITIS | GENE-EXPRESSION | SODIUM-INDUCED COLITIS | CYSTIC-FIBROSIS | INFLAMMATORY BOWEL DISEASES | SPHINGOSINE KINASE | INTESTINAL EPITHELIAL-CELLS | CELL BIOLOGY | Leukocytes, Mononuclear - metabolism | Substrate Specificity | Colitis - pathology | Male | Leukocytes, Mononuclear - immunology | Female | Disease Models, Animal | Ceramides - metabolism | Lipopolysaccharides - toxicity | Cytokines - metabolism | Immunity, Innate - drug effects | Colon - pathology | Mice, Inbred C57BL | Ceramides - analysis | Alkaline Ceramidase - genetics | Colon - metabolism | Dextran Sulfate - toxicity | Mice, Knockout | Alkaline Ceramidase - deficiency | Up-Regulation - drug effects | Colitis - etiology | Animals | Cell Transformation, Neoplastic | Colitis - metabolism | Leukocytes, Mononuclear - cytology | Mice | Inflammatory bowel disease | Enzymes | Tumorigenesis | Cellular biology | Rodents | Immune system | Original
Journal Article
Cancer Research, ISSN 0008-5472, 02/2001, Volume 61, Issue 3, pp. 1233 - 1240
Dysfunction in the physiological pathways of programmed cell death may promote proliferation of malignant tells, and correction of such defects may selectively...
RAT-LIVER | ACTIVATION | CYCLOSPORINE-A | INHIBITION | THERAPY | ONCOLOGY | SPHINGOMYELINASE | COLORECTAL-CANCER | MULTIDRUG-RESISTANCE | C-JUN | RADIATION-INDUCED APOPTOSIS | Liver Neoplasms, Experimental - secondary | Rats, Wistar | Apoptosis - drug effects | Colonic Neoplasms - drug therapy | Humans | Male | Liver Neoplasms, Experimental - prevention & control | Colonic Neoplasms - metabolism | Liver - drug effects | Ceramidases | Growth Inhibitors - pharmacology | Amides - pharmacology | Ceramides - metabolism | Enzyme Inhibitors - pharmacology | Rats | Amidohydrolases - antagonists & inhibitors | Myristates - pharmacology | Ceramides - pharmacology | Sphingosine - pharmacology | Xenograft Model Antitumor Assays | Sphingosine - analogs & derivatives | Animals | Colonic Neoplasms - pathology | Liver - cytology | Mice | Propanolamines - pharmacology
RAT-LIVER | ACTIVATION | CYCLOSPORINE-A | INHIBITION | THERAPY | ONCOLOGY | SPHINGOMYELINASE | COLORECTAL-CANCER | MULTIDRUG-RESISTANCE | C-JUN | RADIATION-INDUCED APOPTOSIS | Liver Neoplasms, Experimental - secondary | Rats, Wistar | Apoptosis - drug effects | Colonic Neoplasms - drug therapy | Humans | Male | Liver Neoplasms, Experimental - prevention & control | Colonic Neoplasms - metabolism | Liver - drug effects | Ceramidases | Growth Inhibitors - pharmacology | Amides - pharmacology | Ceramides - metabolism | Enzyme Inhibitors - pharmacology | Rats | Amidohydrolases - antagonists & inhibitors | Myristates - pharmacology | Ceramides - pharmacology | Sphingosine - pharmacology | Xenograft Model Antitumor Assays | Sphingosine - analogs & derivatives | Animals | Colonic Neoplasms - pathology | Liver - cytology | Mice | Propanolamines - pharmacology
Journal Article
Oncogene, ISSN 0950-9232, 05/2016, Volume 35, Issue 21, p. 2801
Targeting cell motility, which is required for dissemination and metastasis, has therapeutic potential for ovarian cancer metastasis, and regulatory mechanisms...
Care and treatment | Ceramides | Development and progression | Genetic aspects | Phosphotransferases | Health aspects | Ovarian cancer | Lipids | Metastasis | Cellular biology | Kinases
Care and treatment | Ceramides | Development and progression | Genetic aspects | Phosphotransferases | Health aspects | Ovarian cancer | Lipids | Metastasis | Cellular biology | Kinases
Journal Article
FASEB Journal, ISSN 0892-6638, 2001, Volume 15, Issue 14, pp. 2669 - 2679
Our previous results have indicated that the major cellular pool of sphingomyelin present on the outer leaflet of the plasma membrane is not involved in the...
Bcl-2 | Cytochrome c | Ceramide | Mitochondria | Targeting | Apoptosis | PERMEABILITY TRANSITION PORE | CERAMIDE-INDUCED APOPTOSIS | ACTIVATION | mitochondria | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEMBRANES | apoptosis | CELL-SURFACE | DEATH | CELL BIOLOGY | targeting | ceramide | TUMOR-NECROSIS-FACTOR | DISTINCT POOL | BIOLOGY | cytochrome c | CYTOCHROME-C RELEASE | Green Fluorescent Proteins | Sphingomyelin Phosphodiesterase - genetics | Apoptosis - drug effects | Humans | Recombinant Fusion Proteins - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Transfection | Biological Transport | Time Factors | Sphingomyelin Phosphodiesterase - metabolism | Tumor Cells, Cultured | Amino Acid Sequence | Ceramides - metabolism | Sphingomyelins - metabolism | Signal Transduction | Sphingomyelin Phosphodiesterase - pharmacology | Cell Compartmentation - genetics | Mitochondria - metabolism | Cytochrome c Group - secretion | Hydrolysis | Protein Sorting Signals - genetics | Recombinant Fusion Proteins - genetics | Luminescent Proteins - genetics | Apoptosis - physiology | Mutation | Proto-Oncogene Proteins c-bcl-2 - genetics | Luminescent Proteins - metabolism
Bcl-2 | Cytochrome c | Ceramide | Mitochondria | Targeting | Apoptosis | PERMEABILITY TRANSITION PORE | CERAMIDE-INDUCED APOPTOSIS | ACTIVATION | mitochondria | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEMBRANES | apoptosis | CELL-SURFACE | DEATH | CELL BIOLOGY | targeting | ceramide | TUMOR-NECROSIS-FACTOR | DISTINCT POOL | BIOLOGY | cytochrome c | CYTOCHROME-C RELEASE | Green Fluorescent Proteins | Sphingomyelin Phosphodiesterase - genetics | Apoptosis - drug effects | Humans | Recombinant Fusion Proteins - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Transfection | Biological Transport | Time Factors | Sphingomyelin Phosphodiesterase - metabolism | Tumor Cells, Cultured | Amino Acid Sequence | Ceramides - metabolism | Sphingomyelins - metabolism | Signal Transduction | Sphingomyelin Phosphodiesterase - pharmacology | Cell Compartmentation - genetics | Mitochondria - metabolism | Cytochrome c Group - secretion | Hydrolysis | Protein Sorting Signals - genetics | Recombinant Fusion Proteins - genetics | Luminescent Proteins - genetics | Apoptosis - physiology | Mutation | Proto-Oncogene Proteins c-bcl-2 - genetics | Luminescent Proteins - metabolism
Journal Article