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Clinical & Experimental Metastasis, ISSN 0262-0898, 6/2012, Volume 29, Issue 5, pp. 511 - 522
Elastin-rich lung extracellular matrix is largely remodeled during tumor invasion. Elastin degradation produces peptides displaying a wide range of biological... 
Urokinase | Elastin-derived peptides | Biomedicine | Matrix metalloproteinases | Hematology | Cell invasion | Lung cancer | Oncology | Cancer Research | Surgical Oncology | Biomedicine general | MIGRATION | TUMOR INVASION | CARCINOMA CELLS | MONOCYTES | STRUCTURAL-CHARACTERIZATION | RECEPTOR | BINDING PROTEIN | GALECTIN-3 | ONCOLOGY | IN-VIVO | EXPRESSION | Adenocarcinoma - pathology | Cell Proliferation | Oligonucleotide Array Sequence Analysis | Humans | Lung Neoplasms - metabolism | Galectin 3 - metabolism | Extracellular Matrix - metabolism | Lung Neoplasms - pathology | Gene Expression Profiling | Integrin alphaVbeta3 - metabolism | Adenocarcinoma - metabolism | Integrin alphaVbeta3 - genetics | Biomarkers, Tumor - metabolism | Adenocarcinoma - genetics | Real-Time Polymerase Chain Reaction | Lung Neoplasms - genetics | Elastin - metabolism | Matrix Metalloproteinase 2 - metabolism | RNA Processing, Post-Transcriptional - drug effects | RNA, Messenger - genetics | Urokinase-Type Plasminogen Activator - genetics | Galectin 3 - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Matrix Metalloproteinase 2 - genetics | Urokinase-Type Plasminogen Activator - metabolism | Biomarkers, Tumor - genetics | Oligopeptides - pharmacology | Cell Movement | Enzymes | Peptides | RNA | Elastin | Development and progression | Lactose | Messenger RNA | Proteases | Capacity | Analysis | Tumors | Integrins
Journal Article
BMC Genomics, ISSN 1471-2164, 06/2017, Volume 18, Issue 1, pp. 443 - 18
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, p. e0123544
Journal Article
British Journal of Cancer, ISSN 0007-0920, 09/2017, Volume 117, Issue 6, pp. 813 - 825
Background: Hypoxia is negatively associated with glioblastoma (GBM) patient survival and contributes to tumour resistance. Anti-angiogenic therapy in GBM... 
hypoxia | MALIGNANT GLIOMA-CELLS | autophagy | BNIP3 | ATG9A | THERAPEUTIC IMPLICATIONS | DEATH | MULTIFORME | patient-derived xenografts | TEMOZOLOMIDE | chloroquine | BREAST-CANCER CELLS | glioblastoma | METABOLISM | ONCOLOGY | INDUCED CYTOTOXICITY | Neoplasm Transplantation | Bevacizumab - pharmacology | Vesicular Transport Proteins - metabolism | Humans | Neoplasm Proteins - physiology | Autophagy-Related Proteins - physiology | Spheroids, Cellular - pathology | Autophagy - physiology | Brain Neoplasms - blood supply | Gene Expression Profiling | Neoplasm Proteins - metabolism | Autophagy - drug effects | Brain Neoplasms - metabolism | Gene Knockdown Techniques | Vesicular Transport Proteins - physiology | Chloroquine - pharmacology | Heterografts | Membrane Proteins - physiology | Glioblastoma - metabolism | Membrane Proteins - metabolism | Cell Survival - physiology | Molecular Targeted Therapy - methods | Cell Survival - drug effects | Gene Silencing | Angiogenesis Inhibitors - pharmacology | Random Allocation | Brain Neoplasms - drug therapy | Mice, SCID | Tumor Hypoxia - physiology | Drug Synergism | Animals | Cell Line, Tumor | Mice, Inbred NOD | Mice | Glioblastoma - drug therapy | Autophagy-Related Proteins - metabolism | Glioblastoma - blood supply | Cell survival | Chloroquine | Glioblastoma | Pharmacology | In vitro testing | Survival | Autophagy | Bevacizumab | Angiogenesis | Depletion | Inhibitors | Xenografts | Hypoxia | Synergistic effect | Inhibition | Phagocytosis | Tumors | Translational Therapeutics
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2016, Volume 11, Issue 2, p. e0149050
Immunoresponsive gene 1 (IRG1) is one of the highest induced genes in macrophages under pro-inflammatory conditions. Its function has been recently described:... 
MYCOBACTERIUM-TUBERCULOSIS | IFN-BETA | NITRIC-OXIDE PRODUCTION | MULTIDISCIPLINARY SCIENCES | MURINE MACROPHAGES | IMMUNE-RESPONSIVE GENE-1 | PERITONEAL-MACROPHAGES | FACTOR-I | NO SYNTHASE | FACTOR-BINDING SITES | LIPOPOLYSACCHARIDE-INDUCIBLE GENES | Proteins - physiology | Humans | Interferon Regulatory Factor-1 - physiology | Male | Mitochondria - metabolism | Gene Regulatory Networks | Macrophages - enzymology | Protein Transport | Gene Expression Regulation, Enzymologic | Animals | Leukocytes, Mononuclear - immunology | Lipopolysaccharides - pharmacology | Leukocytes, Mononuclear - enzymology | RAW 264.7 Cells | Transcription, Genetic | Mice | Tricarboxylic acid cycle | Regulators | Animal models | Transcription factors | Laboratories | Genomics | Gene regulation | Genes | Infections | Genomes | Interferon regulatory factor 1 | Kinases | Macrophages | Isocitrate lyase | Machinery | Lipopolysaccharides | Machinery and equipment | Proteins | Itaconic acid | Mitochondria | Immunology | Prediction models | Rodents | Bacteria | Immune system | Bacterial infections | siRNA | Inflammation | Tumor necrosis factor-α | Acid production | Metabolism | Gene expression | Aconitic acid | Gene silencing | Acids | Nitric oxide | γ-Interferon | Computer applications | Interferon | Internet | Bypasses | Interferon regulatory factor
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2/2014, Volume 127, Issue 2, pp. 203 - 219
Journal Article
The Journal of experimental medicine, ISSN 0022-1007, 2016, Volume 213, Issue 4, pp. 483 - 497
Journal Article
The Journal of Pathology, ISSN 0022-3417, 08/2017, Volume 242, Issue 4, pp. 421 - 434
HuR regulates cytoplasmic mRNA stability and translatability, and the HuR expression level has been shown to correlate with poor disease outcome in several... 
meningioma | hypoxia | apoptosis | HuR | ELAV‐like 1 | proliferation | ELAV-like 1 | BREAST-CARCINOMA | INCREASED CYCLOOXYGENASE-2 EXPRESSION | FACTOR-A | DELAYED SURGICAL RESECTION | PATHOLOGY | RICH ELEMENTS | OVARIAN-CARCINOMA | COLON-CANCER | FACTOR MESSENGER-RNAS | STABILITY FACTOR HUR | ONCOLOGY | ORAL-CANCER CELLS | Cell Hypoxia - physiology | Prognosis | Humans | Middle Aged | Cytoplasm - metabolism | Male | Meningioma - genetics | Neoplasm Proteins - metabolism | Gene Knockdown Techniques | ELAV-Like Protein 1 - metabolism | Neoplasm Grading | Cell Division | Up-Regulation - physiology | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Retrospective Studies | ELAV-Like Protein 1 - deficiency | Neoplasm Proteins - genetics | Gene Expression Regulation, Neoplastic - physiology | Meningioma - metabolism | ELAV-Like Protein 1 - genetics | Kaplan-Meier Estimate | Gene Expression Profiling - methods | Meningioma - pathology | Cell Line, Tumor | Aged | Biomarkers, Tumor - genetics | Neoplasm Proteins - deficiency | Apoptosis - physiology | Observer Variation | RNA-Binding Proteins - metabolism | RNA | Growth | Analysis | Ribonuclease | Statistics | Meningioma | Protein binding | Ribonuclease A | Cell proliferation | Cell culture | Biotechnology | Poly(A) | Regulations | Deregulation | mRNA processing | Genomes | Tissues | Signal transduction | Cell growth | Cell cycle | Assembly | HuR protein | Cell survival | Splicing | Gene expression | Ribonucleic acid--RNA | Survival | Signaling | RNA-binding protein | Correlation analysis | Medical prognosis | Cell lines | Men | Hypoxia | Poly(A)-specific ribonuclease | In vitro methods and tests | Tumors | mRNA stability | Apoptosis | Cancer
Journal Article