Cancer Treatment Reviews, ISSN 0305-7372, 2014, Volume 40, Issue 6, pp. 750 - 759
Abstract The hedgehog (Hh) pathway is aberrantly activated in a number of tumors. In medulloblastoma, basal cell carcinoma, and rhabdomyosarcoma, mutations in...
Hematology, Oncology and Palliative Medicine | Hedgehog | Smoothened | Combination chemotherapy | Targeted therapy | Novel antitumor agents | Cell signaling | STEM-CELLS | ACTIVATED PROTEIN-KINASE | SELF-RENEWAL | CHRONIC MYELOID-LEUKEMIA | EPITHELIAL-MESENCHYMAL TRANSITION | GLI TRANSCRIPTION FACTORS | ONCOLOGY | BASAL-CELL CARCINOMA | PROSTATE-CANCER | TARGETING HEDGEHOG | SONIC-HEDGEHOG | Hedgehog Proteins - drug effects | Neoplasms - metabolism | TOR Serine-Threonine Kinases - metabolism | Receptors, Notch - metabolism | Humans | Hedgehog Proteins - metabolism | Receptor, Epidermal Growth Factor - drug effects | Phosphatidylinositol 3-Kinases - metabolism | raf Kinases - metabolism | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Receptor, Epidermal Growth Factor - metabolism | Phosphatidylinositol 3-Kinases - drug effects | Proto-Oncogene Proteins c-akt - metabolism | TOR Serine-Threonine Kinases - drug effects | Janus Kinase 2 - antagonists & inhibitors | Molecular Targeted Therapy - methods | Proto-Oncogene Proteins p21(ras) - metabolism | Receptors, Notch - drug effects | Fusion Proteins, bcr-abl - drug effects | Neoplasms - drug therapy | Proto-Oncogene Proteins p21(ras) - drug effects | Animals | MAP Kinase Signaling System - drug effects | Signal Transduction - drug effects | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | raf Kinases - drug effects | Fusion Proteins, bcr-abl - metabolism | Proto-Oncogene Proteins c-akt - drug effects | Receptor Cross-Talk - drug effects | Care and treatment | Health aspects | Leukemia | Analysis | Cancer
Hematology, Oncology and Palliative Medicine | Hedgehog | Smoothened | Combination chemotherapy | Targeted therapy | Novel antitumor agents | Cell signaling | STEM-CELLS | ACTIVATED PROTEIN-KINASE | SELF-RENEWAL | CHRONIC MYELOID-LEUKEMIA | EPITHELIAL-MESENCHYMAL TRANSITION | GLI TRANSCRIPTION FACTORS | ONCOLOGY | BASAL-CELL CARCINOMA | PROSTATE-CANCER | TARGETING HEDGEHOG | SONIC-HEDGEHOG | Hedgehog Proteins - drug effects | Neoplasms - metabolism | TOR Serine-Threonine Kinases - metabolism | Receptors, Notch - metabolism | Humans | Hedgehog Proteins - metabolism | Receptor, Epidermal Growth Factor - drug effects | Phosphatidylinositol 3-Kinases - metabolism | raf Kinases - metabolism | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Receptor, Epidermal Growth Factor - metabolism | Phosphatidylinositol 3-Kinases - drug effects | Proto-Oncogene Proteins c-akt - metabolism | TOR Serine-Threonine Kinases - drug effects | Janus Kinase 2 - antagonists & inhibitors | Molecular Targeted Therapy - methods | Proto-Oncogene Proteins p21(ras) - metabolism | Receptors, Notch - drug effects | Fusion Proteins, bcr-abl - drug effects | Neoplasms - drug therapy | Proto-Oncogene Proteins p21(ras) - drug effects | Animals | MAP Kinase Signaling System - drug effects | Signal Transduction - drug effects | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | raf Kinases - drug effects | Fusion Proteins, bcr-abl - metabolism | Proto-Oncogene Proteins c-akt - drug effects | Receptor Cross-Talk - drug effects | Care and treatment | Health aspects | Leukemia | Analysis | Cancer
Journal Article
Cancer Cell, ISSN 1535-6108, 2010, Volume 17, Issue 4, pp. 388 - 399
In a screen of drugs previously tested in humans we identified itraconazole, a systemic antifungal, as a potent antagonist of the Hedgehog (Hh) signaling...
CHEMBIO | CELLCYCLE | SIGNAL-TRANSDUCTION | STEM-CELLS | CANDIDA-ALBICANS | ONCOLOGY | BASAL-CELL CARCINOMA | PROSTATE-CANCER | MOUSE MODEL | HIGH-DOSE ITRACONAZOLE | LOW-DENSITY-LIPOPROTEIN | DRUG DEVELOPMENT COSTS | PRIMARY CILIUM | Antifungal Agents - pharmacology | Hedgehog Proteins - drug effects | Hedgehog Proteins - chemistry | Humans | Lipoproteins, LDL - physiology | Models, Molecular | Antineoplastic Agents - therapeutic use | Hedgehog Proteins - physiology | Hedgehog Proteins - antagonists & inhibitors | Cell Division - drug effects | Itraconazole - pharmacology | Antifungal Agents - therapeutic use | Itraconazole - therapeutic use | Animals | Signal Transduction - drug effects | Carcinoma, Basal Cell - drug therapy | Mice | Kinetics | Cyclodextrins - pharmacology | Animal models
CHEMBIO | CELLCYCLE | SIGNAL-TRANSDUCTION | STEM-CELLS | CANDIDA-ALBICANS | ONCOLOGY | BASAL-CELL CARCINOMA | PROSTATE-CANCER | MOUSE MODEL | HIGH-DOSE ITRACONAZOLE | LOW-DENSITY-LIPOPROTEIN | DRUG DEVELOPMENT COSTS | PRIMARY CILIUM | Antifungal Agents - pharmacology | Hedgehog Proteins - drug effects | Hedgehog Proteins - chemistry | Humans | Lipoproteins, LDL - physiology | Models, Molecular | Antineoplastic Agents - therapeutic use | Hedgehog Proteins - physiology | Hedgehog Proteins - antagonists & inhibitors | Cell Division - drug effects | Itraconazole - pharmacology | Antifungal Agents - therapeutic use | Itraconazole - therapeutic use | Animals | Signal Transduction - drug effects | Carcinoma, Basal Cell - drug therapy | Mice | Kinetics | Cyclodextrins - pharmacology | Animal models
Journal Article
Cancer Cell, ISSN 1535-6108, 02/2018, Volume 33, Issue 2, pp. 229 - 243.e4
Hedgehog (Hh) pathway inhibitors such as vismodegib are highly effective for treating basal cell carcinoma (BCC); however, residual tumor cells frequently...
skin cancer | basal cell carcinoma | vismodegib | Hedgehog | Notch | HEDGEHOG PATHWAY | STEM-CELLS | VISMODEGIB | ONCOLOGY | HAIR FOLLICLE | ACQUIRED-RESISTANCE | GENOMIC ANALYSIS | SKIN | SOMATIC MUTATIONS | HUMAN HOMOLOG | SMOOTHENED MUTATIONS | CELL BIOLOGY | Hedgehog Proteins - drug effects | Skin Neoplasms - pathology | Skin Neoplasms - drug therapy | Signal Transduction - drug effects | Apoptosis - drug effects | Receptors, Notch - metabolism | Humans | Carcinoma, Basal Cell - drug therapy | Hedgehog Proteins - metabolism | Antineoplastic Agents - pharmacology | Carcinoma, Basal Cell - pathology | Receptors, Notch - drug effects | Basal cell carcinoma | Architecture | Developmental biology | Skin | Drug resistance | Drug therapy | Gene expression
skin cancer | basal cell carcinoma | vismodegib | Hedgehog | Notch | HEDGEHOG PATHWAY | STEM-CELLS | VISMODEGIB | ONCOLOGY | HAIR FOLLICLE | ACQUIRED-RESISTANCE | GENOMIC ANALYSIS | SKIN | SOMATIC MUTATIONS | HUMAN HOMOLOG | SMOOTHENED MUTATIONS | CELL BIOLOGY | Hedgehog Proteins - drug effects | Skin Neoplasms - pathology | Skin Neoplasms - drug therapy | Signal Transduction - drug effects | Apoptosis - drug effects | Receptors, Notch - metabolism | Humans | Carcinoma, Basal Cell - drug therapy | Hedgehog Proteins - metabolism | Antineoplastic Agents - pharmacology | Carcinoma, Basal Cell - pathology | Receptors, Notch - drug effects | Basal cell carcinoma | Architecture | Developmental biology | Skin | Drug resistance | Drug therapy | Gene expression
Journal Article
Medical science monitor : international medical journal of experimental and clinical research, ISSN 1643-3750, 09/2018, Volume 24, pp. 6695 - 6706
Background: The aim of this study was to determine the role of icariin, a Chinese traditional herbal medicine extracted from Epimedium, in osteoarthritis (OA),...
MEDICINE, RESEARCH & EXPERIMENTAL | PROLIFERATION | ARTHRITIS | HISTOPATHOLOGY | CULTURE | Hedgehog Proteins | HYPERTROPHY | BONE-FORMATION | Chondrocytes | BIOLOGY | Osteoarthritis, Knee | DIFFERENTIATION | STROMAL CELLS | Hedgehog Proteins - drug effects | Anterior Cruciate Ligament - drug effects | Mice, Inbred C57BL | Hedgehog Proteins - metabolism | Cartilage - drug effects | Osteoarthritis - drug therapy | Collagen Type II - metabolism | Cartilage, Articular - pathology | Chondrocytes - drug effects | Parathyroid Hormone-Related Protein - drug effects | Animals | Cell Differentiation - drug effects | Cell Proliferation - drug effects | Flavonoids - pharmacology | Mice | Osteoarthritis, Knee - metabolism | Disease Models, Animal
MEDICINE, RESEARCH & EXPERIMENTAL | PROLIFERATION | ARTHRITIS | HISTOPATHOLOGY | CULTURE | Hedgehog Proteins | HYPERTROPHY | BONE-FORMATION | Chondrocytes | BIOLOGY | Osteoarthritis, Knee | DIFFERENTIATION | STROMAL CELLS | Hedgehog Proteins - drug effects | Anterior Cruciate Ligament - drug effects | Mice, Inbred C57BL | Hedgehog Proteins - metabolism | Cartilage - drug effects | Osteoarthritis - drug therapy | Collagen Type II - metabolism | Cartilage, Articular - pathology | Chondrocytes - drug effects | Parathyroid Hormone-Related Protein - drug effects | Animals | Cell Differentiation - drug effects | Cell Proliferation - drug effects | Flavonoids - pharmacology | Mice | Osteoarthritis, Knee - metabolism | Disease Models, Animal
Journal Article
Alcoholism: Clinical and Experimental Research, ISSN 0145-6008, 12/2017, Volume 41, Issue 12, pp. 2051 - 2065
Background Cell and molecular mechanisms mediating the cardiovascular effects of alcohol are not fully understood. Our aim was to determine the effect of...
Stem Cells | Alcohol | Hedgehog | Stem Cell Antigen‐1 | Atherosclerosis | Progenitor Cells | MODERATE | POPULATION | CONTRIBUTE | ISCHEMIC-HEART-DISEASE | PROLIFERATION | SUBSTANCE ABUSE | Stem Cell Antigen-1 | IN-VITRO | ADVENTITIA | SMOOTH-MUSCLE-CELLS | EXPRESSION | CONSUMPTION | Carotid Arteries - drug effects | Hedgehog Proteins - drug effects | Stem Cells - immunology | Gene Expression - drug effects | Cell Proliferation - physiology | Membrane Proteins - immunology | Mice, Transgenic | Hedgehog Proteins - physiology | Animals | Patched-1 Receptor - biosynthesis | Antigens, Ly - immunology | Carotid Arteries - physiopathology | Cell Differentiation - drug effects | Veratrum Alkaloids - pharmacology | Stem Cells - physiology | Vascular Remodeling - physiology | Cell Proliferation - drug effects | Mice | Vascular Remodeling - drug effects | Zinc Finger Protein Gli2 - biosynthesis | Antigens | Analysis | Stem cells | Fluorescence | Genetic engineering | Gene expression | Differentiation (biology) | Transgenic | Stem cell transplantation | Smooth muscle | Remodeling | Alcohols | Allografts | Ataxin | Rodents | Inhibition | Carotid artery | Expansion | Injury analysis | Thickening | Ethanol | Muscles | Blood vessels | Patched protein | Polymerase chain reaction | Signaling | Molecular modelling | Hedgehog protein | Green fluorescent protein | Cells (biology)
Stem Cells | Alcohol | Hedgehog | Stem Cell Antigen‐1 | Atherosclerosis | Progenitor Cells | MODERATE | POPULATION | CONTRIBUTE | ISCHEMIC-HEART-DISEASE | PROLIFERATION | SUBSTANCE ABUSE | Stem Cell Antigen-1 | IN-VITRO | ADVENTITIA | SMOOTH-MUSCLE-CELLS | EXPRESSION | CONSUMPTION | Carotid Arteries - drug effects | Hedgehog Proteins - drug effects | Stem Cells - immunology | Gene Expression - drug effects | Cell Proliferation - physiology | Membrane Proteins - immunology | Mice, Transgenic | Hedgehog Proteins - physiology | Animals | Patched-1 Receptor - biosynthesis | Antigens, Ly - immunology | Carotid Arteries - physiopathology | Cell Differentiation - drug effects | Veratrum Alkaloids - pharmacology | Stem Cells - physiology | Vascular Remodeling - physiology | Cell Proliferation - drug effects | Mice | Vascular Remodeling - drug effects | Zinc Finger Protein Gli2 - biosynthesis | Antigens | Analysis | Stem cells | Fluorescence | Genetic engineering | Gene expression | Differentiation (biology) | Transgenic | Stem cell transplantation | Smooth muscle | Remodeling | Alcohols | Allografts | Ataxin | Rodents | Inhibition | Carotid artery | Expansion | Injury analysis | Thickening | Ethanol | Muscles | Blood vessels | Patched protein | Polymerase chain reaction | Signaling | Molecular modelling | Hedgehog protein | Green fluorescent protein | Cells (biology)
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2016, Volume 113, Issue 47, pp. E7545 - E7553
Inflammation disrupts tissue architecture and function, thereby contributing to the pathogenesis of diverse diseases; the signals that promote or restrict...
Inflammatory bowel disease | Hedgehog signaling | Colon cancer | Colitis | Interleukin-10 | STEM-CELLS | colitis | colon cancer | ADENOCARCINOMA | MULTIDISCIPLINARY SCIENCES | INTERLEUKIN-10 RECEPTOR | MOUSE | PROLIFERATION | interleukin-10 | FOXP3 | inflammatory bowel disease | BOWEL-DISEASE | REGULATORY T-CELLS | MICE | CANCER PROGRESSION | Hedgehog Proteins - drug effects | Small Molecule Libraries - pharmacology | T-Lymphocytes, Regulatory - metabolism | Small Molecule Libraries - administration & dosage | Zinc Finger Protein GLI1 - genetics | Humans | Dextran Sulfate - adverse effects | Hedgehog Proteins - metabolism | Disease Progression | Animals | Signal Transduction - drug effects | Forkhead Transcription Factors - metabolism | Colitis - chemically induced | Colitis - metabolism | Interleukin-10 - metabolism | Colitis - drug therapy | Mice | Mutation | CD4 Antigens - metabolism | Disease Models, Animal | Biological Sciences | PNAS Plus
Inflammatory bowel disease | Hedgehog signaling | Colon cancer | Colitis | Interleukin-10 | STEM-CELLS | colitis | colon cancer | ADENOCARCINOMA | MULTIDISCIPLINARY SCIENCES | INTERLEUKIN-10 RECEPTOR | MOUSE | PROLIFERATION | interleukin-10 | FOXP3 | inflammatory bowel disease | BOWEL-DISEASE | REGULATORY T-CELLS | MICE | CANCER PROGRESSION | Hedgehog Proteins - drug effects | Small Molecule Libraries - pharmacology | T-Lymphocytes, Regulatory - metabolism | Small Molecule Libraries - administration & dosage | Zinc Finger Protein GLI1 - genetics | Humans | Dextran Sulfate - adverse effects | Hedgehog Proteins - metabolism | Disease Progression | Animals | Signal Transduction - drug effects | Forkhead Transcription Factors - metabolism | Colitis - chemically induced | Colitis - metabolism | Interleukin-10 - metabolism | Colitis - drug therapy | Mice | Mutation | CD4 Antigens - metabolism | Disease Models, Animal | Biological Sciences | PNAS Plus
Journal Article
Lancet Oncology, ISSN 1470-2045, 2004, Volume 5, Issue 4, pp. 209 - 218
Medulloblastoma is the most common malignant brain tumour that occurs during childhood. Multimodality treatment regimens have substantially improved survival...
ADJUVANT CHEMOTHERAPY | PRIMITIVE NEUROECTODERMAL TUMORS | METASTATIC-DISEASE | ONCOLOGY | SONIC HEDGEHOG | SPORADIC MEDULLOBLASTOMAS | CENTRAL-NERVOUS-SYSTEM | CHILDRENS CANCER GROUP | BETA-CATENIN | BASAL-CELL CARCINOMAS | HUMAN HOMOLOG | Proto-Oncogene Proteins - pharmacology | Cerebellar Neoplasms - drug therapy | Proto-Oncogene Proteins - drug effects | Prognosis | Signal Transduction | Humans | Risk Factors | Zebrafish Proteins | Wnt Proteins | Proto-Oncogene Proteins - biosynthesis | Hedgehog Proteins | Medulloblastoma - pathology | Trans-Activators - biosynthesis | Trans-Activators - pharmacology | Cerebellar Neoplasms - pathology | Medulloblastoma - drug therapy | Receptor, Epidermal Growth Factor - physiology | Care and treatment | Medulloblastoma | Brain tumors | Cancer
ADJUVANT CHEMOTHERAPY | PRIMITIVE NEUROECTODERMAL TUMORS | METASTATIC-DISEASE | ONCOLOGY | SONIC HEDGEHOG | SPORADIC MEDULLOBLASTOMAS | CENTRAL-NERVOUS-SYSTEM | CHILDRENS CANCER GROUP | BETA-CATENIN | BASAL-CELL CARCINOMAS | HUMAN HOMOLOG | Proto-Oncogene Proteins - pharmacology | Cerebellar Neoplasms - drug therapy | Proto-Oncogene Proteins - drug effects | Prognosis | Signal Transduction | Humans | Risk Factors | Zebrafish Proteins | Wnt Proteins | Proto-Oncogene Proteins - biosynthesis | Hedgehog Proteins | Medulloblastoma - pathology | Trans-Activators - biosynthesis | Trans-Activators - pharmacology | Cerebellar Neoplasms - pathology | Medulloblastoma - drug therapy | Receptor, Epidermal Growth Factor - physiology | Care and treatment | Medulloblastoma | Brain tumors | Cancer
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 04/2018, Volume 149, pp. 110 - 121
Embryonic stem cell pathways such as hedgehog and Wnt pathways are central to the tumorigenic properties of cancer stem cells (CSC). Since CSCs are...
Smoothened | Wnt signaling pathway | Porcupine | Stem cell | Cancer therapy | Hedgehog signaling pathway | Antagonist | DESIGN | CHEMISTRY, MEDICINAL | RECEPTOR | IDENTIFICATION | SMOOTHENED ANTAGONISTS | CANCER-THERAPY | CLINICAL-IMPLICATIONS | OPTIMIZATION | BINDING | FUSED 3-RING SYSTEM | PORCUPINE INHIBITORS | Acyltransferases - antagonists & inhibitors | Hedgehog Proteins - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Hedgehog Proteins - metabolism | Structure-Activity Relationship | Animals | Wnt Signaling Pathway - drug effects | Membrane Proteins - antagonists & inhibitors | Signal Transduction - drug effects | Drug Design | Antineoplastic Agents - pharmacology | Mice | Smoothened Receptor - antagonists & inhibitors | Index Medicus
Smoothened | Wnt signaling pathway | Porcupine | Stem cell | Cancer therapy | Hedgehog signaling pathway | Antagonist | DESIGN | CHEMISTRY, MEDICINAL | RECEPTOR | IDENTIFICATION | SMOOTHENED ANTAGONISTS | CANCER-THERAPY | CLINICAL-IMPLICATIONS | OPTIMIZATION | BINDING | FUSED 3-RING SYSTEM | PORCUPINE INHIBITORS | Acyltransferases - antagonists & inhibitors | Hedgehog Proteins - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Hedgehog Proteins - metabolism | Structure-Activity Relationship | Animals | Wnt Signaling Pathway - drug effects | Membrane Proteins - antagonists & inhibitors | Signal Transduction - drug effects | Drug Design | Antineoplastic Agents - pharmacology | Mice | Smoothened Receptor - antagonists & inhibitors | Index Medicus
Journal Article
Journal of Clinical Periodontology, ISSN 0303-6979, 01/2015, Volume 42, Issue 1, pp. 29 - 36
Objective Cyclosporine‐A (CsA)‐induced gingival overgrowth may arise from an alteration in stoma matrix homeostasis. Sonic hedgehog (Shh) plays a key role...
collagen | Sonic hedgehog | gingival fibroblasts | transforming growth factor‐beta | cyclosporine‐A | transforming growth factor-beta | cyclosporine-A | TRANSCRIPTION FACTORS | CELLS | MYOFIBROBLAST | PROLIFERATION | EPITHELIAL-MESENCHYMAL TRANSITION | RENAL FIBROSIS | GROWTH-FACTOR-BETA | IN-VITRO | DENTISTRY, ORAL SURGERY & MEDICINE | TRANSFORMING GROWTH-FACTOR-BETA-1 | NEPHROTOXICITY | Hedgehog Proteins - drug effects | Cell Line | Cyclosporine - pharmacology | Extracellular Matrix - drug effects | Humans | Transforming Growth Factor beta - physiology | Actins - drug effects | Hedgehog Proteins - physiology | Hedgehog Proteins - antagonists & inhibitors | Transforming Growth Factor beta - drug effects | Gingiva - drug effects | Signal Transduction - drug effects | Time Factors | Fibroblasts - drug effects | Gingiva - cytology | Veratrum Alkaloids - pharmacology | Collagen Type I - drug effects | Transforming Growth Factor beta - antagonists & inhibitors | Cell Culture Techniques | Homeostasis - drug effects | Immunosuppressive Agents - pharmacology | Receptor Cross-Talk - drug effects
collagen | Sonic hedgehog | gingival fibroblasts | transforming growth factor‐beta | cyclosporine‐A | transforming growth factor-beta | cyclosporine-A | TRANSCRIPTION FACTORS | CELLS | MYOFIBROBLAST | PROLIFERATION | EPITHELIAL-MESENCHYMAL TRANSITION | RENAL FIBROSIS | GROWTH-FACTOR-BETA | IN-VITRO | DENTISTRY, ORAL SURGERY & MEDICINE | TRANSFORMING GROWTH-FACTOR-BETA-1 | NEPHROTOXICITY | Hedgehog Proteins - drug effects | Cell Line | Cyclosporine - pharmacology | Extracellular Matrix - drug effects | Humans | Transforming Growth Factor beta - physiology | Actins - drug effects | Hedgehog Proteins - physiology | Hedgehog Proteins - antagonists & inhibitors | Transforming Growth Factor beta - drug effects | Gingiva - drug effects | Signal Transduction - drug effects | Time Factors | Fibroblasts - drug effects | Gingiva - cytology | Veratrum Alkaloids - pharmacology | Collagen Type I - drug effects | Transforming Growth Factor beta - antagonists & inhibitors | Cell Culture Techniques | Homeostasis - drug effects | Immunosuppressive Agents - pharmacology | Receptor Cross-Talk - drug effects
Journal Article
Cell Proliferation, ISSN 0960-7722, 12/2018, Volume 51, Issue 6, pp. e12500 - n/a
Objectives The sonic hedgehog (Shh) signalling pathway has an important role in the maintenance of various stem cells and organogenesis during development....
IN-VITRO | STEM-CELLS | ACTIVATION | SMO | PATHWAY | GROWTH | DIFFERENTIATION | TUMORIGENICITY | CELL BIOLOGY | Hedgehog Proteins - drug effects | Skin - cytology | Apoptosis - drug effects | Neoplastic Stem Cells - drug effects | Purines - pharmacology | Hedgehog Proteins - metabolism | Morpholines - pharmacology | Epithelial-Mesenchymal Transition - drug effects | Veratrum Alkaloids - metabolism | Animals | Neoplastic Stem Cells - metabolism | Signal Transduction - drug effects | Cell Line, Tumor | Female | Cell Proliferation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Developmental biology | Skin | Stem cells | Cell proliferation | Phenotypes | Mesenchyme | Stem cell transplantation | Gene expression | Organogenesis | Signal transduction | Signaling | Precursors | Hedgehog protein | Immunofluorescence | Recombinant | Apoptosis
IN-VITRO | STEM-CELLS | ACTIVATION | SMO | PATHWAY | GROWTH | DIFFERENTIATION | TUMORIGENICITY | CELL BIOLOGY | Hedgehog Proteins - drug effects | Skin - cytology | Apoptosis - drug effects | Neoplastic Stem Cells - drug effects | Purines - pharmacology | Hedgehog Proteins - metabolism | Morpholines - pharmacology | Epithelial-Mesenchymal Transition - drug effects | Veratrum Alkaloids - metabolism | Animals | Neoplastic Stem Cells - metabolism | Signal Transduction - drug effects | Cell Line, Tumor | Female | Cell Proliferation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Developmental biology | Skin | Stem cells | Cell proliferation | Phenotypes | Mesenchyme | Stem cell transplantation | Gene expression | Organogenesis | Signal transduction | Signaling | Precursors | Hedgehog protein | Immunofluorescence | Recombinant | Apoptosis
Journal Article
European Cells and Materials, ISSN 1473-2262, 2012, Volume 23, pp. 121 - 134
Hydrostatic pressure (HP) is a key component of the in vivo joint environment and has been shown to enhance chondrogenesis of stem cells. The objective of this...
Cartilage | Transforming growth factor (TGF)-β3 | Synovial membrane | Hydrostatic pressure | Chondrocytes | Infrapatellar fat pad | Stem cells | stem cells | MATERIALS SCIENCE, BIOMATERIALS | chondrocytes | transforming growth factor (TGF)-beta 3 | BIOCHEMISTRY & MOLECULAR BIOLOGY | cartilage | infrapatellar fat pad | synovial membrane | Hedgehog Proteins - drug effects | Chondrogenesis - drug effects | Hedgehog Proteins - metabolism | Stem Cells - cytology | Patellofemoral Joint - metabolism | Stem Cells - metabolism | Chondrocytes - drug effects | Collagen Type X - metabolism | Swine | Cartilage - cytology | Chondrocytes - metabolism | Transforming Growth Factor beta3 - administration & dosage | Collagen Type X - drug effects | SOX9 Transcription Factor - metabolism | Glycosaminoglycans - metabolism | Cells, Cultured | SOX9 Transcription Factor - drug effects | Patellofemoral Joint - cytology | Cartilage - metabolism | Hydrostatic Pressure | Synovial Membrane - metabolism | Phenotype | Animals | Cell Differentiation - drug effects | Stem Cells - drug effects | Synovial Membrane - cytology | transforming growth factor (TGF)-β3
Cartilage | Transforming growth factor (TGF)-β3 | Synovial membrane | Hydrostatic pressure | Chondrocytes | Infrapatellar fat pad | Stem cells | stem cells | MATERIALS SCIENCE, BIOMATERIALS | chondrocytes | transforming growth factor (TGF)-beta 3 | BIOCHEMISTRY & MOLECULAR BIOLOGY | cartilage | infrapatellar fat pad | synovial membrane | Hedgehog Proteins - drug effects | Chondrogenesis - drug effects | Hedgehog Proteins - metabolism | Stem Cells - cytology | Patellofemoral Joint - metabolism | Stem Cells - metabolism | Chondrocytes - drug effects | Collagen Type X - metabolism | Swine | Cartilage - cytology | Chondrocytes - metabolism | Transforming Growth Factor beta3 - administration & dosage | Collagen Type X - drug effects | SOX9 Transcription Factor - metabolism | Glycosaminoglycans - metabolism | Cells, Cultured | SOX9 Transcription Factor - drug effects | Patellofemoral Joint - cytology | Cartilage - metabolism | Hydrostatic Pressure | Synovial Membrane - metabolism | Phenotype | Animals | Cell Differentiation - drug effects | Stem Cells - drug effects | Synovial Membrane - cytology | transforming growth factor (TGF)-β3
Journal Article
International Journal of Cancer, ISSN 0020-7136, 07/2004, Volume 110, Issue 6, pp. 831 - 837
Hedgehog (Hh) signalling controls many aspects of development. It also regulates cell growth and differentiation in adult tissues and is activated in a number...
hedgehog | cyclopamine | colon cancer | Hedgehog | Colon cancer | Cyclopamine | TRANSDUCTION | INTESTINE | CANCER | INHIBITION | REGIONALIZATION | ONCOLOGY | PATHWAY | ADENOMA | DIFFERENTIATION | MUTATIONS | SONIC-HEDGEHOG | Proto-Oncogene Proteins - drug effects | Carcinoma | Apoptosis - drug effects | Humans | Proto-Oncogene Proteins - genetics | Wnt Proteins | Adenoma | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Intestinal Mucosa - drug effects | Trans-Activators - physiology | Hedgehog Proteins | Signal Transduction - drug effects | Colonic Neoplasms - pathology | Proto-Oncogene Proteins - physiology | Trans-Activators - genetics | Veratrum Alkaloids - pharmacology | Cell Line, Tumor | Signal Transduction - physiology | Rectal Neoplasms - pathology | Intestinal Mucosa - pathology
hedgehog | cyclopamine | colon cancer | Hedgehog | Colon cancer | Cyclopamine | TRANSDUCTION | INTESTINE | CANCER | INHIBITION | REGIONALIZATION | ONCOLOGY | PATHWAY | ADENOMA | DIFFERENTIATION | MUTATIONS | SONIC-HEDGEHOG | Proto-Oncogene Proteins - drug effects | Carcinoma | Apoptosis - drug effects | Humans | Proto-Oncogene Proteins - genetics | Wnt Proteins | Adenoma | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Intestinal Mucosa - drug effects | Trans-Activators - physiology | Hedgehog Proteins | Signal Transduction - drug effects | Colonic Neoplasms - pathology | Proto-Oncogene Proteins - physiology | Trans-Activators - genetics | Veratrum Alkaloids - pharmacology | Cell Line, Tumor | Signal Transduction - physiology | Rectal Neoplasms - pathology | Intestinal Mucosa - pathology
Journal Article