Pharmaceuticals (Basel, Switzerland), ISSN 1424-8247, 06/2019, Volume 12, Issue 2, p. 92
Improvements in cancer therapy frequently stem from the development of new small-molecule inhibitors, paralleled by the identification of biomarkers that can...
mediator complex | CDK8 | cancer
mediator complex | CDK8 | cancer
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 4/2018, Volume 55, Issue 4, pp. 3490 - 3498
Parkinson’s disease (PD) is the second most common neurodegenerative disorder. Accumulating evidences suggest that PD might have a strong neurodevelopmental...
Neurology | Neurosciences | Biomedicine | LRRK2 | Neurobiology | miRNA activity | Neuronal differentiation | TRIM32 | Parkinson’s disease | Cell Biology | Parkinson's disease | Cell fate | Neurodegenerative diseases | Therapeutic applications | MiRNA | Leucine | Inhibition | Mutation | LRRK2 protein | Kinases | Movement disorders
Neurology | Neurosciences | Biomedicine | LRRK2 | Neurobiology | miRNA activity | Neuronal differentiation | TRIM32 | Parkinson’s disease | Cell Biology | Parkinson's disease | Cell fate | Neurodegenerative diseases | Therapeutic applications | MiRNA | Leucine | Inhibition | Mutation | LRRK2 protein | Kinases | Movement disorders
Journal Article
Neoplasia, ISSN 1476-5586, 06/2018, Volume 20, Issue 6, pp. 632 - 642
Leukemic stem cells (LSCs) are an emerging target of curative anti-leukemia therapy. In acute lymphoblastic leukemia (ALL), LSCs frequently express CD34 and...
INITIATING CELLS | STEM-CELLS | THERAPY | COMPLETE REMISSION | ONCOLOGY | PHILADELPHIA-CHROMOSOME | TYROSINE KINASE | IMATINIB | CHRONIC MYELOID-LEUKEMIA | PRIMITIVE HEMATOPOIETIC-CELL | TRANSPLANTATION | Cell Line | Antigens, CD34 - metabolism | Humans | Leukemia, Myeloid, Acute - metabolism | Stem Cells - metabolism | Gene Expression Regulation, Leukemic - physiology | Animals | Neoplastic Stem Cells - metabolism | Biomarkers, Tumor - metabolism | Leukemia, Myelogenous, Chronic, BCR-ABL Positive - metabolism | ADP-ribosyl Cyclase 1 - metabolism | Female | Mice, Inbred NOD | Mice | Flow cytometry | CD26 antigen | Leukemia | Antibodies | Stem cell transplantation | Interleukin 1 receptors | CD44 antigen | CD38 antigen | Xenografts | CD25 antigen | CD123 antigen | CD34 antigen | Interleukin 2 receptors | Phenotypes | CD19 antigen | Acute lymphatic leukemia | Myeloid leukemia | Chronic myeloid leukemia | Lymphatic leukemia | Progenitor cells | CXCR4 protein | CD22 antigen | Stem cells | Phenotyping | CD20 antigen | CD18 antigen
INITIATING CELLS | STEM-CELLS | THERAPY | COMPLETE REMISSION | ONCOLOGY | PHILADELPHIA-CHROMOSOME | TYROSINE KINASE | IMATINIB | CHRONIC MYELOID-LEUKEMIA | PRIMITIVE HEMATOPOIETIC-CELL | TRANSPLANTATION | Cell Line | Antigens, CD34 - metabolism | Humans | Leukemia, Myeloid, Acute - metabolism | Stem Cells - metabolism | Gene Expression Regulation, Leukemic - physiology | Animals | Neoplastic Stem Cells - metabolism | Biomarkers, Tumor - metabolism | Leukemia, Myelogenous, Chronic, BCR-ABL Positive - metabolism | ADP-ribosyl Cyclase 1 - metabolism | Female | Mice, Inbred NOD | Mice | Flow cytometry | CD26 antigen | Leukemia | Antibodies | Stem cell transplantation | Interleukin 1 receptors | CD44 antigen | CD38 antigen | Xenografts | CD25 antigen | CD123 antigen | CD34 antigen | Interleukin 2 receptors | Phenotypes | CD19 antigen | Acute lymphatic leukemia | Myeloid leukemia | Chronic myeloid leukemia | Lymphatic leukemia | Progenitor cells | CXCR4 protein | CD22 antigen | Stem cells | Phenotyping | CD20 antigen | CD18 antigen
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 10/2019, Volume 10, Issue 1, pp. 1 - 15
Cyclin-dependent kinases (CDKs) are frequently deregulated in cancer and represent promising drug targets. We provide evidence that CDK8 has a key role in...
TARGET | AML CELLS | PALBOCICLIB | POTENT | INHIBITION | SET ENRICHMENT ANALYSIS | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | B-CELL COMMITMENT | SERINE PHOSPHORYLATION | CANCER | TOR protein | BCR protein | Deregulation | Animal models | Transcription | Leukemia | Cyclin-dependent kinases | Cyclin-dependent kinase 8 | Maintenance | Kinases | Latency | Degradation | Signal transduction | Cell death | Inhibition | Chemical synthesis | Acute myeloid leukemia | Index Medicus
TARGET | AML CELLS | PALBOCICLIB | POTENT | INHIBITION | SET ENRICHMENT ANALYSIS | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | B-CELL COMMITMENT | SERINE PHOSPHORYLATION | CANCER | TOR protein | BCR protein | Deregulation | Animal models | Transcription | Leukemia | Cyclin-dependent kinases | Cyclin-dependent kinase 8 | Maintenance | Kinases | Latency | Degradation | Signal transduction | Cell death | Inhibition | Chemical synthesis | Acute myeloid leukemia | Index Medicus
Journal Article
British Journal of Haematology, ISSN 0007-1048, 10/2017, Volume 179, Issue 2, pp. 229 - 241
Summary The p21‐activated kinases (PAKs) are key nodes in oncogenic signalling pathways controlling growth, survival, and motility of cancer cells. Their...
CML | p21‐activated kinases | BCR/ABL1 | PAK2 | exosomes | lymphoma | p21-activated kinases | TRANSFORMATION | PROTEIN | CANCER CELLS | PHOSPHORYLATION | TUMOR SURVEILLANCE | IN-VIVO | STAT5 | LEUKEMIA | HEMATOLOGY | EXPRESSION | Exosomes - metabolism | Cell Proliferation | Leukemia - pathology | Humans | Extracellular Matrix - metabolism | Exosomes - genetics | Exosomes - pathology | Hematologic Neoplasms - pathology | Leukemia - metabolism | Neovascularization, Pathologic - pathology | Lymphoma - metabolism | Extracellular Matrix - genetics | Lymphoma - pathology | Hematologic Neoplasms - metabolism | Leukemia - genetics | p21-Activated Kinases - genetics | Endothelial Cells - metabolism | Lymphoma - genetics | p21-Activated Kinases - metabolism | Fusion Proteins, bcr-abl - genetics | Animals | Cell Line, Tumor | Mice, Inbred NOD | Neovascularization, Pathologic - genetics | Hematologic Neoplasms - genetics | Mice | Neovascularization, Pathologic - metabolism | Endothelial Cells - pathology | Extracellular Matrix - pathology | Fusion Proteins, bcr-abl - metabolism | Methylcellulose | Lymphomas | Analysis | Leukemia | Endothelium | Cell proliferation | Deregulation | Cell survival | Hematology | Colonies | Medical treatment | Malignancy | Exosomes | Kinases | Endothelial cells | Vascularization | Signal transduction | Signaling | Cell growth | Medical prognosis | Isoforms | Extracellular matrix | Conditioning | Tumors | Cancer | Apoptosis | Index Medicus | BCR | Haematological Malignancy | ABL1 | Research Paper
CML | p21‐activated kinases | BCR/ABL1 | PAK2 | exosomes | lymphoma | p21-activated kinases | TRANSFORMATION | PROTEIN | CANCER CELLS | PHOSPHORYLATION | TUMOR SURVEILLANCE | IN-VIVO | STAT5 | LEUKEMIA | HEMATOLOGY | EXPRESSION | Exosomes - metabolism | Cell Proliferation | Leukemia - pathology | Humans | Extracellular Matrix - metabolism | Exosomes - genetics | Exosomes - pathology | Hematologic Neoplasms - pathology | Leukemia - metabolism | Neovascularization, Pathologic - pathology | Lymphoma - metabolism | Extracellular Matrix - genetics | Lymphoma - pathology | Hematologic Neoplasms - metabolism | Leukemia - genetics | p21-Activated Kinases - genetics | Endothelial Cells - metabolism | Lymphoma - genetics | p21-Activated Kinases - metabolism | Fusion Proteins, bcr-abl - genetics | Animals | Cell Line, Tumor | Mice, Inbred NOD | Neovascularization, Pathologic - genetics | Hematologic Neoplasms - genetics | Mice | Neovascularization, Pathologic - metabolism | Endothelial Cells - pathology | Extracellular Matrix - pathology | Fusion Proteins, bcr-abl - metabolism | Methylcellulose | Lymphomas | Analysis | Leukemia | Endothelium | Cell proliferation | Deregulation | Cell survival | Hematology | Colonies | Medical treatment | Malignancy | Exosomes | Kinases | Endothelial cells | Vascularization | Signal transduction | Signaling | Cell growth | Medical prognosis | Isoforms | Extracellular matrix | Conditioning | Tumors | Cancer | Apoptosis | Index Medicus | BCR | Haematological Malignancy | ABL1 | Research Paper
Journal Article
MOLECULAR NEUROBIOLOGY, ISSN 0893-7648, 04/2018, Volume 55, Issue 4, pp. 3490 - 3498
Parkinson's disease (PD) is the second most common neurodegenerative disorder. Accumulating evidences suggest that PD might have a strong neurodevelopmental...
NEURAL STEM-CELLS | Parkinson'sdisease | LRRK2 | miRNA activity | Neuronal differentiation | DIFFERENTIATION | TRIM32 | NEUROSCIENCES | Neurons - pathology | Argonaute Proteins - metabolism | Humans | Mice, Inbred C57BL | Ubiquitin-Protein Ligases - metabolism | MicroRNAs - metabolism | Parkinson Disease - genetics | Mutation - genetics | Animals | HEK293 Cells | RNA-Induced Silencing Complex - metabolism | Protein Binding | Cell Differentiation | MicroRNAs - genetics | Neurons - metabolism | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - metabolism | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics | Neurons | MicroRNA
NEURAL STEM-CELLS | Parkinson'sdisease | LRRK2 | miRNA activity | Neuronal differentiation | DIFFERENTIATION | TRIM32 | NEUROSCIENCES | Neurons - pathology | Argonaute Proteins - metabolism | Humans | Mice, Inbred C57BL | Ubiquitin-Protein Ligases - metabolism | MicroRNAs - metabolism | Parkinson Disease - genetics | Mutation - genetics | Animals | HEK293 Cells | RNA-Induced Silencing Complex - metabolism | Protein Binding | Cell Differentiation | MicroRNAs - genetics | Neurons - metabolism | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - metabolism | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics | Neurons | MicroRNA
Journal Article
British Journal of Haematology, ISSN 0007-1048, 10/2017, Volume 179, Issue 2, pp. 229 - 241
Journal Article
Stem Cells and Development, ISSN 1547-3287, 09/2013, Volume 22, Issue 18, pp. 2487 - 2496
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene cause familial as well as sporadic Parkinson's disease (PD) that is characterized by an...
Original Research Reports | MOUSE-BRAIN | MEDICINE, RESEARCH & EXPERIMENTAL | LOCALIZATION | PROGENITORS | LEUCINE-RICH-REPEAT-KINASE-2 | NUCLEAR RECEPTOR TLX | SELF-RENEWAL | CELL & TISSUE ENGINEERING | TRANSPLANTATION | PATHOGENESIS | MICRORNA-9 | PATHWAY | MICE | HEMATOLOGY | Parkinson Disease - therapy | Protein-Serine-Threonine Kinases - deficiency | Up-Regulation | Humans | Cell Survival - genetics | MicroRNAs - metabolism | Gene Expression Profiling | Neural Stem Cells - cytology | Cell Differentiation - genetics | Mitochondria - genetics | Base Sequence | Parkinson Disease - metabolism | Oxidation-Reduction | Down-Regulation | Mice, Inbred C57BL | Cells, Cultured | Oxidative Stress - genetics | Protein-Serine-Threonine Kinases - genetics | Mitochondria - metabolism | Cell- and Tissue-Based Therapy | Parkinson Disease - genetics | Sequence Analysis, DNA | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Mice, Knockout | Animals | Mice | MicroRNAs - genetics | Mutation | Neural Stem Cells - metabolism | Parkinson's disease | Research | Gene mutations | Analysis | Stem cells
Original Research Reports | MOUSE-BRAIN | MEDICINE, RESEARCH & EXPERIMENTAL | LOCALIZATION | PROGENITORS | LEUCINE-RICH-REPEAT-KINASE-2 | NUCLEAR RECEPTOR TLX | SELF-RENEWAL | CELL & TISSUE ENGINEERING | TRANSPLANTATION | PATHOGENESIS | MICRORNA-9 | PATHWAY | MICE | HEMATOLOGY | Parkinson Disease - therapy | Protein-Serine-Threonine Kinases - deficiency | Up-Regulation | Humans | Cell Survival - genetics | MicroRNAs - metabolism | Gene Expression Profiling | Neural Stem Cells - cytology | Cell Differentiation - genetics | Mitochondria - genetics | Base Sequence | Parkinson Disease - metabolism | Oxidation-Reduction | Down-Regulation | Mice, Inbred C57BL | Cells, Cultured | Oxidative Stress - genetics | Protein-Serine-Threonine Kinases - genetics | Mitochondria - metabolism | Cell- and Tissue-Based Therapy | Parkinson Disease - genetics | Sequence Analysis, DNA | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Mice, Knockout | Animals | Mice | MicroRNAs - genetics | Mutation | Neural Stem Cells - metabolism | Parkinson's disease | Research | Gene mutations | Analysis | Stem cells
Journal Article
Cancer Immunology Research, ISSN 2326-6066, 04/2018, Volume 6, Issue 4, pp. 458 - 466
Cyclin-dependent kinase 8 (CDK8) is a member of the transcription-regulating CDK family. CDK8 activates or represses transcription by associating with the...
REGULATOR | ONCOLOGY | REJECTION | KINASE | CATENIN | STAT1 TRANSACTIVATION DOMAIN | IMMUNOLOGY | SERINE PHOSPHORYLATION | MATURATION | INHIBITOR | TUMOR SURVEILLANCE | CANCER | Mice, Transgenic | Immunity, Innate | Cell Differentiation - genetics | Killer Cells, Natural - cytology | Animals | Melanoma, Experimental | Neoplasms - genetics | Neoplasms - immunology | Gene Deletion | Cell Line, Tumor | Cyclin-Dependent Kinase 8 - genetics | Killer Cells, Natural - immunology | Mice | Killer Cells, Natural - metabolism | Neoplasms - pathology | Cytotoxicity, Immunologic | Disease Models, Animal
REGULATOR | ONCOLOGY | REJECTION | KINASE | CATENIN | STAT1 TRANSACTIVATION DOMAIN | IMMUNOLOGY | SERINE PHOSPHORYLATION | MATURATION | INHIBITOR | TUMOR SURVEILLANCE | CANCER | Mice, Transgenic | Immunity, Innate | Cell Differentiation - genetics | Killer Cells, Natural - cytology | Animals | Melanoma, Experimental | Neoplasms - genetics | Neoplasms - immunology | Gene Deletion | Cell Line, Tumor | Cyclin-Dependent Kinase 8 - genetics | Killer Cells, Natural - immunology | Mice | Killer Cells, Natural - metabolism | Neoplasms - pathology | Cytotoxicity, Immunologic | Disease Models, Animal
Journal Article
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