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Cancer and metastasis reviews, ISSN 1573-7233, 2019, Volume 38, Issue 3, pp. 417 - 430
In the past decade, immune-based therapies such as monoclonal antibodies against tumor epitopes or immune checkpoint inhibitors have become an integral part of... 
CX3CR1 | T-CELL MIGRATION | FRACTALKINE RECEPTOR CXCR1 | Dipeptiyl peptidase 4 | Matrix metalloproteinases | Tumor-infiltrating lymphocytes | CX3CL1 FRACTALKINE | IFN-GAMMA | Cathepsins | TRANSMEMBRANE CHEMOKINES | BREAST-CANCER | LUNG METASTASIS | MURINE MODEL | CXC CHEMOKINE | ONCOLOGY | Proteases | CXCR3 | ANTITUMOR IMMUNITY | Chemokines | CX3C Chemokine Receptor 1 - immunology | Chemokine CXCL11 - chemistry | Neoplasms - metabolism | Chemokine CXCL10 - chemistry | Chemokine CXCL9 - chemistry | Humans | Lymphocytes, Tumor-Infiltrating - enzymology | CX3C Chemokine Receptor 1 - metabolism | Proteolysis | Chemokine CXCL10 - immunology | Lymphocytes, Tumor-Infiltrating - metabolism | Chemokine CXCL11 - immunology | Chemokines - immunology | Peptide Hydrolases - metabolism | Amino Acid Sequence | Receptors, CXCR3 - metabolism | Models, Molecular | Neoplasms - enzymology | Chemokine CXCL9 - immunology | Chemokines - chemistry | Animals | Lymphocytes, Tumor-Infiltrating - pathology | Neoplasms - immunology | Chemokine CXCL9 - metabolism | Receptors, CXCR3 - immunology | Chemokines - metabolism | Chemokine CXCL11 - metabolism | Neoplasms - pathology | Chemokine CXCL10 - metabolism | Lymphocytes, Tumor-Infiltrating - immunology | Animal models | Target recognition | Effector cells | CX3CR1 protein | Leukocytes | Matrix metalloproteinase | Inactivation | Metastases | Lymphocytes | Cleavage | Peptidase | Deactivation | CXCR3 protein | Epitopes | Immune checkpoint | Monoclonal antibodies | Infiltration | Solid tumors | Cancer | Tumors
Journal Article
Journal of Leukocyte Biology, ISSN 0741-5400, 1999, Volume 66, Issue 3, pp. 489 - 494
Upon exposure to immune or inflammatory stimuli, dendritic cells (DC) migrate from peripheral tissues to lymphoid organs, where they present antigen. The... 
Chemokime receptors | Transmigration | CD34-derived DC | Chemotaxis | MIGRATION | RECRUITMENT | LUNG | chemokine receptors | MACROPHAGE-DERIVED CHEMOKINE | CORECEPTORS | transmigration | RECEPTOR EXPRESSION | IMMUNOLOGY | MATURATION | CUTTING EDGE | CELL BIOLOGY | IN-VITRO | HEMATOLOGY | chemotaxis | Monocyte Chemoattractant Proteins - pharmacology | Receptors, CCR5 - genetics | Chemokine CCL22 | Membrane Proteins - pharmacology | Receptors, CCR5 - biosynthesis | RNA, Messenger - biosynthesis | Receptors, Chemokine - biosynthesis | Chemokines, CXC - pharmacology | Dendritic Cells - drug effects | Mice, Inbred DBA | Chemokines - pharmacology | Receptors, Chemokine - genetics | Receptors, Cytokine - genetics | Hematopoietic Stem Cells - drug effects | Chemokine CCL19 | Chemokine CXCL12 | Chemokine CCL4 | Chemokines, CC - pharmacology | Cytokines | Receptors, Cytokine - biosynthesis | Membrane Glycoproteins - pharmacology | RNA, Messenger - genetics | Receptors, CCR7 | Chemokine CCL7 | Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology | Chemotaxis - drug effects | Down-Regulation - drug effects | Gene Expression Regulation - drug effects | Up-Regulation - drug effects | Tumor Necrosis Factor-alpha - pharmacology | Animals | Chemokine CCL5 - pharmacology | Chemokine CCL2 - pharmacology | Mice | CD40 Ligand | Receptors, CCR1 | Receptors, CCR2 | Macrophage Inflammatory Proteins - pharmacology
Journal Article
Journal Article
The Journal of biological chemistry, ISSN 1083-351X, 2011, Volume 286, Issue 9, pp. 7214 - 7226
The Ca2+-binding protein of the EF-hand type, S100B, is abundantly expressed in and secreted by astrocytes, and release of S100B from damaged astrocytes occurs... 
CYTOPLASMIC DOMAIN | IN-VITRO | ACTIVATION | NEURITE OUTGROWTH | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | NITRIC-OXIDE | RECEPTOR | GROWTH-FACTOR | RHO-GTPASES | GLYCATION END-PRODUCTS | Microglia - metabolism | Chemokine CCL3 - immunology | Nerve Growth Factors - metabolism | S100 Proteins - immunology | Cell Movement - immunology | S100 Proteins - genetics | Chemokine CXCL12 - genetics | Microglia - immunology | Chemokine CCL3 - genetics | Calcium-Binding Proteins - immunology | Cattle | Encephalitis - metabolism | Chemokine CCL3 - metabolism | Chemokine CCL5 - metabolism | Receptors, Immunologic - immunology | Receptor for Advanced Glycation End Products | Chemokine CXCL12 - immunology | Chemokines - immunology | Calcium-Binding Proteins - metabolism | Microglia - cytology | Recombinant Proteins - metabolism | Cell Line | S100 Calcium Binding Protein beta Subunit | Mice, Inbred C57BL | Rats | Encephalitis - immunology | S100 Proteins - metabolism | Nerve Growth Factors - immunology | Recombinant Proteins - genetics | Chemokines - genetics | Animals | Carrier Proteins - metabolism | Chemokine CXCL12 - metabolism | Recombinant Proteins - immunology | Up-Regulation - immunology | Nerve Growth Factors - genetics | Chemokine CCL5 - genetics | Cytoskeleton - metabolism | Chemokines - metabolism | Mice | Receptors, Immunologic - genetics | Chemokine CCL5 - immunology | Receptors, Immunologic - metabolism | Calcium-Binding Proteins - genetics | Index Medicus | Immunology | Defensins | Signal Transduction | Neurodegeneration | Migration | Calcium-binding Proteins | Innate Immunity | RAGE | S100B | Chemokines | Microglia
Journal Article
Nature (London), ISSN 1476-4687, 2015, Volume 527, Issue 7577, pp. 249 - 253
Epigenetic silencing including histone modifications and DNA methylation is an important tumorigenic mechanism. However, its role in cancer immunopathology and... 
Polycomb Repressive Complex 2 - antagonists & inhibitors | CD8-Positive T-Lymphocytes - cytology | Immunotherapy - methods | Prognosis | Histones - chemistry | Chemokine CXCL9 - biosynthesis | Humans | Ovarian Neoplasms - pathology | DNA (Cytosine-5-)-Methyltransferases - antagonists & inhibitors | Th1 Cells - immunology | DNA (Cytosine-5-)-Methyltransferases - metabolism | Th1 Cells - metabolism | Chemokine CXCL10 - biosynthesis | Chemokine CXCL10 - immunology | Female | Epigenesis, Genetic - drug effects | Lysine - metabolism | Tumor Cells, Cultured | Chemokines - immunology | Tumor Escape - immunology | Chemokines - biosynthesis | DNA (Cytosine-5-)-Methyltransferase 1 | Gene Silencing | Chemokine CXCL9 - immunology | Chemokine CXCL9 - genetics | Chemokines - genetics | Enhancer of Zeste Homolog 2 Protein | Ovarian Neoplasms - enzymology | Xenograft Model Antitumor Assays | B7-H1 Antigen - metabolism | Animals | Chemokine CXCL10 - genetics | Ovarian Neoplasms - therapy | Mice | Histones - metabolism | CD8-Positive T-Lymphocytes - immunology | Polycomb Repressive Complex 2 - metabolism | DNA Methylation - drug effects | Lymphocytes, Tumor-Infiltrating - immunology | Ovarian Neoplasms - immunology | checkpoint | CXCL9 | histone modification | chemotherapy | epigenetics | Chemokine | CXCL10 | DNMT | T cell therapy | DNA methylation | PD-L1 | B7-H1 | cancer | trafficking | PD-1 | EZH2
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2012, Volume 336, Issue 6086, pp. 1317 - 1321
Journal Article
Journal Article