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Photochemistry and Photobiology, ISSN 0031-8655, 07/2017, Volume 93, Issue 4, pp. 1016 - 1024
Naproxen possesses anti‐proliferative and pro‐apoptotic effects besides its known anti‐inflammatory functions. Here, we demonstrate the anticancer effects of... 
APOPTOSIS | BIOPHYSICS | NONSTEROIDAL ANTIINFLAMMATORY DRUGS | INDUCED SKIN CARCINOGENESIS | SIGNALING PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUTANT P53 | ENDOPLASMIC-RETICULUM STRESS | NF-KAPPA-B | CANCER | PHOTOCARCINOGENESIS | PROSTAGLANDIN E-2 | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Neoplasms, Radiation-Induced - etiology | Naproxen - pharmacology | Patched-1 Receptor - genetics | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Skin Neoplasms - prevention & control | Ultraviolet Rays | Carcinoma, Basal Cell - etiology | Epithelial-Mesenchymal Transition | Biomarkers, Tumor - metabolism | Carcinoma, Basal Cell - prevention & control | Female | Neoplasms, Radiation-Induced - prevention & control | Antineoplastic Agents - pharmacology | Neoplasms, Radiation-Induced - pathology | Skin Neoplasms - pathology | Mice, Hairless | Mice, Transgenic | Carcinoma, Basal Cell - pathology | Carcinoma, Squamous Cell - prevention & control | Unfolded Protein Response | Neoplasms, Radiation-Induced - metabolism | Carcinoma, Basal Cell - metabolism | Skin Neoplasms - metabolism | Carcinoma, Squamous Cell - etiology | Animals | Cell Line, Tumor | Skin Neoplasms - etiology | Squamous cell carcinoma | Naproxen | Analysis | Skin cancer | Vimentin | Animal models | Mesenchyme | Cyclin D1 | Carcinogenesis | E-cadherin | Anticancer properties | Carcinogens | N-Cadherin | Protein folding | Proliferating cell nuclear antigen | Inhibition | Invasiveness | Inflammation | Hairless | Ablation | Nitric-oxide synthase | Ultraviolet radiation | Skin | Cyclooxygenase-2 | Tumors | Cancer | Apoptosis | Index Medicus | UVB | skin | photocarcinogenesis | inflammation | UPR signaling
Journal Article
Cancer Cell, ISSN 1535-6108, 2011, Volume 19, Issue 1, pp. 114 - 124
Journal Article
Cancer Cell, ISSN 1535-6108, 02/2014, Volume 25, Issue 2, pp. 139 - 151
We report that two oncogenes coamplified on chromosome 3q26, and , cooperate to drive a stem-like phenotype in lung squamous cell carcinoma (LSCC). Protein... 
INITIATING CELLS | DETECTS FREQUENT | STEM-CELLS | PROTEIN | CANCER CELLS | EPITHELIUM | ONCOLOGY | TRANSFORMED GROWTH | PKC-IOTA | KINASE-C-IOTA | BASAL-CELLS | CELL BIOLOGY | Acyltransferases - antagonists & inhibitors | Protein Kinase C - genetics | RNA, Small Interfering - genetics | Cell Proliferation | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Lung Neoplasms - metabolism | SOXB1 Transcription Factors - antagonists & inhibitors | Lung Neoplasms - pathology | Acyltransferases - metabolism | Acyltransferases - genetics | Promoter Regions, Genetic - genetics | Immunoenzyme Techniques | SOXB1 Transcription Factors - metabolism | Neoplastic Stem Cells - metabolism | SOXB1 Transcription Factors - genetics | Cell Transformation, Neoplastic - genetics | Isoenzymes - metabolism | Protein Kinase C - metabolism | Neoplastic Stem Cells - pathology | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Tumor Cells, Cultured | Real-Time Polymerase Chain Reaction | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Signal Transduction | Carcinoma, Non-Small-Cell Lung - genetics | Isoenzymes - genetics | RNA, Messenger - genetics | Carcinoma, Non-Small-Cell Lung - metabolism | Protein Kinase C - antagonists & inhibitors | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Animals | High-Throughput Nucleotide Sequencing | Mice | Cell Transformation, Neoplastic - pathology | Isoenzymes - antagonists & inhibitors | Apoptosis | Squamous cell carcinoma | Genetic aspects | Cancer | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 5, pp. e10431 - e10431
Prostate epithelial cells from both normal and cancer tissues, grown in three-dimensional (3D) culture as spheroids, represent promising in vitro models for... 
EPITHELIAL-MESENCHYMAL TRANSITION | BREAST-CANCER | GENE-EXPRESSION SIGNATURE | STEM-CELLS | MAMMARY EPITHELIA | METASTASIS | BIOLOGY | TUMOR-CELL INVASION | DIFFERENTIATION | CULTURE MODEL | LINES | Laminin - pharmacology | Epithelial Cells - drug effects | Humans | Mesoderm - drug effects | Spheroids, Cellular - pathology | Male | Antineoplastic Agents - therapeutic use | Phosphatidylinositol 3-Kinases - metabolism | Spheroids, Cellular - enzymology | Neoplasm Proteins - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | RNA, Messenger - metabolism | Prostate - pathology | Prostatic Neoplasms - genetics | Cell Transformation, Neoplastic - genetics | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Prostate - drug effects | Antineoplastic Agents - pharmacology | Collagen - pharmacology | Spheroids, Cellular - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Tumor Cells, Cultured | Proto-Oncogene Proteins c-akt - metabolism | Principal Component Analysis | Prostatic Neoplasms - drug therapy | Epithelium - drug effects | Prostatic Neoplasms - pathology | Epithelium - pathology | Neoplasm Invasiveness | Intracellular Signaling Peptides and Proteins - antagonists & inhibitors | RNA, Messenger - genetics | Epithelial Cells - pathology | Cell Shape - drug effects | Phenotype | Proteoglycans - pharmacology | Signal Transduction - drug effects | Models, Biological | Prostatic Neoplasms - enzymology | Cell Proliferation - drug effects | TOR Serine-Threonine Kinases | Cell Transformation, Neoplastic - pathology | Mesoderm - pathology | Drug Combinations | Proto-Oncogene Proteins c-akt - antagonists & inhibitors | Epigenetic inheritance | Growth | Oncology, Experimental | Genes | Research | Gene expression | Ionizing radiation | Stem cells | Physiological aspects | Models | Drug discovery | Drug therapy | Prostate cancer | Integrins | Cancer | Cell culture | Biotechnology | Transformation | Motility | Leukocyte migration | Mesenchyme | Epithelial cells | Homeostasis | AKT protein | Metastasis | Drug resistance | Tissues | Ovarian cancer | Cell adhesion & migration | Metastases | Rodents | Fibroblasts | Extracellular matrix | Basal lamina | Lipid metabolism | Medical research | Invasiveness | Phenotypic plasticity | Cultures | Tumor cell lines | Metabolism | Spheroids | 1-Phosphatidylinositol 3-kinase | Signaling | Interferon | Three dimensional models | Prostate | Cell migration | Index Medicus
Journal Article
2006, Medical Intelligence Unit, ISBN 9780387260464, 137
This book provides a comprehensive, highly readable overview of our current knowledge of the molecular pathology of basal cell and squamous cell carcinomas.... 
Squamous cell carcinoma | Skin | Genetic aspects | Basal cell carcinoma | Cancer | Pathology | Cancer Research | Oncology | Biomedicine
Book
American Journal of Respiratory Cell and Molecular Biology, ISSN 1044-1549, 09/2016, Volume 55, Issue 3, pp. 323 - 336
The application of conditional reprogramming culture (CRC) methods to nasal airway epithelial cells would allow more widespread incorporation of primary airway... 
Conditionally reprogrammed cells | Y-27632 | Airway stem progenitor | Clone-forming cell frequency | airway stem progenitor | STEM-CELLS | REGENERATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | conditionally reprogrammed cells | RECEPTOR | PROLIFERATION | PATHOLOGY | BASAL-CELLS | CELL BIOLOGY | IN-VITRO | ROCK INHIBITOR | EPITHELIAL-CELLS | RESPIRATORY SYSTEM | clone-forming cell frequency | ASTHMA | NIH 3T3 Cells | Epithelial Cells - metabolism | Epithelial Cells - drug effects | Humans | Extracellular Matrix - metabolism | Stem Cells - cytology | Lung - cytology | Cell Differentiation - genetics | Cell-Matrix Junctions - metabolism | Clone Cells | Cell Culture Techniques | Epithelial Cells - cytology | Bronchi - cytology | Cellular Reprogramming - genetics | Amides - pharmacology | Extracellular Matrix - drug effects | Transcriptome - drug effects | Transcriptome - genetics | Nose - cytology | Cell-Matrix Junctions - drug effects | Cellular Reprogramming - drug effects | Gene Expression Regulation - drug effects | Animals | Cell Differentiation - drug effects | Fibroblasts - drug effects | Cell Communication - drug effects | Culture Media - pharmacology | Fibroblasts - cytology | Mice | Pyridines - pharmacology | Flow cytometry | Transcription factors | Lung diseases | Cloning | Cystic fibrosis | Gene expression | Asthma | Studies | Cell growth | Pulmonary fibrosis | Cell cycle | Chronic obstructive pulmonary disease | Growth factors | Methods | Index Medicus | Major Technical Advances
Journal Article
eLife, ISSN 2050-084X, 03/2015, Volume 2015, Issue 4, pp. 1 - 25
Recent breakthroughs in 3-dimensional (3D) organoid cultures for many organ systems have led to new physiologically complex in vitro models to study human... 
EXPRESSION PATTERNS | PROGENITOR CELLS | HUMAN AIRWAY EPITHELIUM | VENTRAL FOREGUT | BIOLOGY | BRANCHING MORPHOGENESIS | DEFINITIVE ENDODERM | EXTRACELLULAR-MATRIX | MOUSE LUNG | CLUSTER-ANALYSIS | BASAL-CELLS | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Humans | Gene Expression Profiling | Spheroids, Cellular - cytology | Lung - cytology | Cell Culture Techniques - methods | Cell Differentiation - genetics | Endoderm - cytology | Organoids - metabolism | Organoids - ultrastructure | Lung - metabolism | Induced Pluripotent Stem Cells - cytology | Induced Pluripotent Stem Cells - metabolism | Cell Line | Microscopy, Electron, Transmission | Reproducibility of Results | Pluripotent Stem Cells - cytology | Tissue Engineering - methods | Spheroids, Cellular - metabolism | Cells, Cultured | Organoids - cytology | Reverse Transcriptase Polymerase Chain Reaction | Endoderm - metabolism | Organogenesis | Pluripotent Stem Cells - metabolism | Microscopy, Confocal | Lung - embryology | Cluster analysis | Mesenchyme | Transcription | Developmental biology | Lung | Lung diseases | Fetuses | Embryo cells | Basal cells | Principal components analysis | Smooth muscle | Genomes | Epithelium | Ribonucleic acid--RNA | Spheroids | Children & youth | Respiratory tract | Hospitals | Organoids | Stem cells | Alveoli | Pluripotency | Foregut | Index Medicus
Journal Article
Nature Cell Biology, ISSN 1465-7392, 03/2010, Volume 12, Issue 3, pp. 299 - 305
For most types of cancers, the cell at the origin of tumour initiation is still unknown. Here, we used mouse genetics to identify cells at the origin of basal... 
POPULATION | STEM-CELLS | SONIC HEDGEHOG | EPIDERMIS | HAIR FOLLICLE BULGE | KERATINOCYTES | CANCER | EXPRESSION | HUMAN HOMOLOG | MOUSE SKIN | CELL BIOLOGY | Epithelial Cells - metabolism | Cadherins - metabolism | Receptors, G-Protein-Coupled - metabolism | Skin - metabolism | Cell Count | Ear, External - pathology | Integrin beta4 - metabolism | Tail - pathology | Hair Follicle - pathology | Hedgehog Proteins - genetics | Neoplastic Stem Cells - metabolism | Kruppel-Like Transcription Factors - metabolism | Smoothened Receptor | Neoplastic Stem Cells - pathology | Cell Differentiation | Patched Receptors | Skin - pathology | Keratin-10 - metabolism | Epidermis - metabolism | Epidermis - pathology | RNA, Untranslated | Bacterial Proteins - genetics | Receptors, Cell Surface - metabolism | Epithelial Cells - pathology | Genes, Reporter - genetics | Mice, Transgenic | Carcinoma, Basal Cell - pathology | Mice, Inbred Strains | Clone Cells - metabolism | Keratin-14 - genetics | Carcinoma, Basal Cell - metabolism | Keratin-15 - metabolism | Keratin-19 - genetics | Proteins - genetics | Cell Lineage | Animals | Clone Cells - pathology | Proteins - metabolism | Models, Biological | Hair Follicle - metabolism | Bacterial Proteins - metabolism | Luminescent Proteins - genetics | Mice | Receptors, G-Protein-Coupled - genetics | Integrases - genetics | Keratin-15 - genetics | Luminescent Proteins - metabolism | Basal cell carcinoma | Stem cells | Genetic aspects | Cellular signal transduction | Research | Health aspects | Risk factors | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 2009, Volume 4, Issue 12, pp. e8248 - e8248
The bronchioles of the murine lung are lined by a simple columnar epithelium composed of ciliated, Clara, and goblet cells that together mediate barrier... 
STEM-CELLS | AIRWAY | EPITHELIAL-CELLS | MOUSE TRACHEA | MULTIPOTENT | BIOLOGY | LUNG MORPHOGENESIS | TRANSCRIPTION FACTOR-I | EXPRESSION | RESPIRATORY EPITHELIUM | BASAL-CELLS | Cell Count | Humans | Goblet Cells - drug effects | Protein Transport - drug effects | Smad3 Protein - metabolism | Uteroglobin - metabolism | Goblet Cells - metabolism | Promoter Regions, Genetic - genetics | Cilia - metabolism | Luciferases - genetics | SOXB1 Transcription Factors - metabolism | Animals | Allergens - immunology | Signal Transduction - drug effects | Cell Differentiation - drug effects | Forkhead Transcription Factors - metabolism | Gene Deletion | Bronchioles - cytology | Cilia - drug effects | Cell Proliferation - drug effects | Mice | Mucoproteins - metabolism | Transforming Growth Factor beta1 - pharmacology | Goblet Cells - cytology | Bone morphogenetic proteins | Tubulins | Transforming growth factors | Cell differentiation | Mucins | Cell proliferation | Pediatrics | Allergens | Transcription factors | Transcription | Lung | Differentiation (biology) | Homeostasis | Mucus | Smad3 protein | Thyroid gland | Biology | Respiratory tract | Morphogenesis | Proteins | Tubulin | Chronic obstructive pulmonary disease | Growth factors | Goblet cells | Markers | Breast cancer | Gene expression | Epithelium | Children & youth | Medicine | Calcitonin gene-related peptide | Hospitals | Stem cells | Cells (biology) | Niches | Tumors | Index Medicus
Journal Article