Journal of Thoracic and Cardiovascular Surgery, The, ISSN 0022-5223, 2012, Volume 144, Issue 1, pp. 33 - 38
Objective Lung cancer is the leading cause of cancer death in North America. Low-dose computed tomography screening can reduce lung cancer–specific mortality...
Cardiothoracic Surgery | SURGERY | RESPIRATORY SYSTEM | CARDIAC & CARDIOVASCULAR SYSTEMS | Smoking - adverse effects | United States - epidemiology | Tomography, X-Ray Computed - standards | Age Factors | Risk Assessment | Comorbidity | Humans | Middle Aged | Risk Factors | Mass Screening - standards | Radiation Dosage | Advisory Committees | Lung Neoplasms - epidemiology | Canada - epidemiology | Smoking - epidemiology | Lung Neoplasms - diagnostic imaging | Aged | Population Surveillance | Thoracic Surgical Procedures - standards | CT imaging | Medical colleges | Surgery | Oncology, Experimental | Lung cancer | Tomography | Diagnosis | Research | Health aspects | Cancer
Cardiothoracic Surgery | SURGERY | RESPIRATORY SYSTEM | CARDIAC & CARDIOVASCULAR SYSTEMS | Smoking - adverse effects | United States - epidemiology | Tomography, X-Ray Computed - standards | Age Factors | Risk Assessment | Comorbidity | Humans | Middle Aged | Risk Factors | Mass Screening - standards | Radiation Dosage | Advisory Committees | Lung Neoplasms - epidemiology | Canada - epidemiology | Smoking - epidemiology | Lung Neoplasms - diagnostic imaging | Aged | Population Surveillance | Thoracic Surgical Procedures - standards | CT imaging | Medical colleges | Surgery | Oncology, Experimental | Lung cancer | Tomography | Diagnosis | Research | Health aspects | Cancer
Journal Article
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Full Text
Whole-animal mounts of Caenorhabditis elegans for 3D imaging using atomic force microscopy
Nanomedicine: Nanotechnology, Biology, and Medicine, ISSN 1549-9634, 2015, Volume 11, Issue 8, pp. 1971 - 1974
Abstract The 3D surface of Caenorhabditis elegans was imaged at nanometer resolution using atomic force microscopy (AFM). Oscillation of a medium stiffness...
Internal Medicine | AFM | Atomic force microscopy | C. elegans | MEDICINE, RESEARCH & EXPERIMENTAL | NANOSCIENCE & NANOTECHNOLOGY | C-ELEGANS | Caenorhabditis elegans - ultrastructure | Animals | Caenorhabditis elegans - genetics | Imaging, Three-Dimensional - methods | Microscopy, Atomic Force - methods | Mutation | Caenorhabditis elegans - anatomy & histology | Caenorhabditis elegans | Nematoda | Microscope and microscopy | atomic force microscopy
Internal Medicine | AFM | Atomic force microscopy | C. elegans | MEDICINE, RESEARCH & EXPERIMENTAL | NANOSCIENCE & NANOTECHNOLOGY | C-ELEGANS | Caenorhabditis elegans - ultrastructure | Animals | Caenorhabditis elegans - genetics | Imaging, Three-Dimensional - methods | Microscopy, Atomic Force - methods | Mutation | Caenorhabditis elegans - anatomy & histology | Caenorhabditis elegans | Nematoda | Microscope and microscopy | atomic force microscopy
Journal Article
Journal of Thoracic and Cardiovascular Surgery, The, ISSN 0022-5223, 2012, Volume 144, Issue 1, pp. 25 - 32
Objective The study objective was to establish The American Association for Thoracic Surgery (AATS) lung cancer screening guidelines for clinical practice....
Cardiothoracic Surgery | CT imaging | Medical colleges | Surgery | Oncology, Experimental | Lung cancer | Tomography | Diagnosis | Research | Cancer
Cardiothoracic Surgery | CT imaging | Medical colleges | Surgery | Oncology, Experimental | Lung cancer | Tomography | Diagnosis | Research | Cancer
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2011, Volume 12, Issue 11, pp. 1004 - 1012
Summary Background ALK gene rearrangement defines a new molecular subtype of non-small-cell lung cancer (NSCLC). In a recent phase 1 clinical trial, the ALK...
Hematology, Oncology and Palliative Medicine | ANAPLASTIC LYMPHOMA KINASE | GEFITINIB | ONCOLOGY | EML4-ALK FUSION GENE | PHASE-III | 2P23 | HISTOLOGY | TUMORS | ACTIVATING MUTATIONS | Lung Neoplasms - drug therapy | Pyrazoles - therapeutic use | Lung Neoplasms - mortality | United States | Humans | Middle Aged | Lung Neoplasms - pathology | Male | Antineoplastic Agents - therapeutic use | Patient Selection | Multicenter Studies as Topic | Time Factors | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Retrospective Studies | Pyridines - therapeutic use | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Lung Neoplasms - enzymology | Risk Assessment | Carcinoma, Non-Small-Cell Lung - genetics | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Survival Rate | Treatment Outcome | Carcinoma, Non-Small-Cell Lung - mortality | Receptor Protein-Tyrosine Kinases - genetics | Protein Kinase Inhibitors - therapeutic use | Gene Rearrangement | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Carcinoma, Non-Small-Cell Lung - enzymology | Australia | Clinical Trials, Phase I as Topic | Care and treatment | Analysis | Patient outcomes | Genetic research | Genetic aspects | Lung cancer, Non-small cell | Cancer
Hematology, Oncology and Palliative Medicine | ANAPLASTIC LYMPHOMA KINASE | GEFITINIB | ONCOLOGY | EML4-ALK FUSION GENE | PHASE-III | 2P23 | HISTOLOGY | TUMORS | ACTIVATING MUTATIONS | Lung Neoplasms - drug therapy | Pyrazoles - therapeutic use | Lung Neoplasms - mortality | United States | Humans | Middle Aged | Lung Neoplasms - pathology | Male | Antineoplastic Agents - therapeutic use | Patient Selection | Multicenter Studies as Topic | Time Factors | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Retrospective Studies | Pyridines - therapeutic use | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Lung Neoplasms - enzymology | Risk Assessment | Carcinoma, Non-Small-Cell Lung - genetics | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Survival Rate | Treatment Outcome | Carcinoma, Non-Small-Cell Lung - mortality | Receptor Protein-Tyrosine Kinases - genetics | Protein Kinase Inhibitors - therapeutic use | Gene Rearrangement | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Carcinoma, Non-Small-Cell Lung - enzymology | Australia | Clinical Trials, Phase I as Topic | Care and treatment | Analysis | Patient outcomes | Genetic research | Genetic aspects | Lung cancer, Non-small cell | Cancer
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2012, Volume 13, Issue 10, pp. 1011 - 1019
Summary Background ALK fusion genes occur in a subset of non-small-cell lung cancers (NSCLCs). We assessed the tolerability and activity of crizotinib in...
Hematology, Oncology and Palliative Medicine | KRAS MUTATIONS | ONCOLOGY | EML4-ALK FUSION GENE | C-MET | KINASE | ACQUIRED-RESISTANCE | ANAPLASTIC LYMPHOMA | CLINICAL-FEATURES | INHIBITOR | REARRANGEMENTS | EGFR | Lung Neoplasms - drug therapy | Pyrazoles - therapeutic use | Lung Neoplasms - enzymology | Lung Neoplasms - mortality | Humans | Middle Aged | Male | Protein Kinase Inhibitors - adverse effects | Carcinoma, Non-Small-Cell Lung - mortality | Pyridines - adverse effects | Protein Kinase Inhibitors - therapeutic use | Aged, 80 and over | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Receptor Protein-Tyrosine Kinases - analysis | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Carcinoma, Non-Small-Cell Lung - enzymology | Pyrazoles - adverse effects | Pyridines - therapeutic use | Care and treatment | Safety and security measures | Genes | Oncology, Experimental | Research | Lung cancer, Non-small cell | Cancer
Hematology, Oncology and Palliative Medicine | KRAS MUTATIONS | ONCOLOGY | EML4-ALK FUSION GENE | C-MET | KINASE | ACQUIRED-RESISTANCE | ANAPLASTIC LYMPHOMA | CLINICAL-FEATURES | INHIBITOR | REARRANGEMENTS | EGFR | Lung Neoplasms - drug therapy | Pyrazoles - therapeutic use | Lung Neoplasms - enzymology | Lung Neoplasms - mortality | Humans | Middle Aged | Male | Protein Kinase Inhibitors - adverse effects | Carcinoma, Non-Small-Cell Lung - mortality | Pyridines - adverse effects | Protein Kinase Inhibitors - therapeutic use | Aged, 80 and over | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Receptor Protein-Tyrosine Kinases - analysis | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Carcinoma, Non-Small-Cell Lung - enzymology | Pyrazoles - adverse effects | Pyridines - therapeutic use | Care and treatment | Safety and security measures | Genes | Oncology, Experimental | Research | Lung cancer, Non-small cell | Cancer
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2016, Volume 17, Issue 12, pp. 1683 - 1696
Summary Background Anaplastic lymphoma kinase ( ALK ) gene rearrangements are oncogenic drivers of non-small-cell lung cancer (NSCLC). Brigatinib (AP26113) is...
Hematology, Oncology and Palliative Medicine | CRIZOTINIB-RESISTANT | ONCOLOGY | CERITINIB | TYROSINE KINASE | DOSE PROPORTIONALITY | ALECTINIB | BRAIN METASTASES | EXPERIENCE | INHIBITORS | MUTATIONS | CHEMOTHERAPY | Lung Neoplasms - genetics | Lung Neoplasms - drug therapy | Organophosphorus Compounds - adverse effects | Carcinoma, Non-Small-Cell Lung - genetics | Humans | Middle Aged | Organophosphorus Compounds - therapeutic use | Male | Protein Kinase Inhibitors - adverse effects | Receptor Protein-Tyrosine Kinases - genetics | Protein Kinase Inhibitors - therapeutic use | Pyrimidines - therapeutic use | Gene Rearrangement | Pyrimidines - adverse effects | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Medical colleges | Lymphomas | Research institutes | Lung cancer, Non-small cell
Hematology, Oncology and Palliative Medicine | CRIZOTINIB-RESISTANT | ONCOLOGY | CERITINIB | TYROSINE KINASE | DOSE PROPORTIONALITY | ALECTINIB | BRAIN METASTASES | EXPERIENCE | INHIBITORS | MUTATIONS | CHEMOTHERAPY | Lung Neoplasms - genetics | Lung Neoplasms - drug therapy | Organophosphorus Compounds - adverse effects | Carcinoma, Non-Small-Cell Lung - genetics | Humans | Middle Aged | Organophosphorus Compounds - therapeutic use | Male | Protein Kinase Inhibitors - adverse effects | Receptor Protein-Tyrosine Kinases - genetics | Protein Kinase Inhibitors - therapeutic use | Pyrimidines - therapeutic use | Gene Rearrangement | Pyrimidines - adverse effects | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Medical colleges | Lymphomas | Research institutes | Lung cancer, Non-small cell
Journal Article
Cancer, ISSN 0008-543X, 09/2011, Volume 117, Issue 17, pp. 3889 - 3899
Currently, nonsmall‐cell lung cancer (NSCLC) is the leading cause of cancer‐related death in the United States. Angiogenesis, the formation of new vasculature,...
antiangiogenic therapy | fibroblast growth factor | NSCLC | angiogenesis | vascular endothelial growth factor | platelet‐derived growth factor | biomarker | platelet-derived growth factor | TARGETED THERAPY | COLLAGEN-XVIII | MICROVESSEL DENSITY | TUMOR ANGIOGENESIS | ADHESION MOLECULES | FACTOR RECEPTOR | VEGF MESSENGER-RNA | ONCOLOGY | SERUM-LEVELS | PATIENT SURVIVAL | CLINICAL-SIGNIFICANCE | Lung Neoplasms - drug therapy | Prognosis | Biomarkers, Tumor - analysis | Carcinoma, Non-Small-Cell Lung - blood supply | Humans | Carcinoma, Non-Small-Cell Lung - metabolism | Neovascularization, Pathologic | Vascular Endothelial Growth Factor A - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Receptors, Vascular Endothelial Growth Factor - metabolism | Angiogenesis Inhibitors - therapeutic use | Carcinoma, Non-Small-Cell Lung - drug therapy | Angiogenic Proteins - metabolism | Lung Neoplasms - blood supply | Care and treatment | Lung cancer | Physiological aspects | Causes of | Neovascularization | Research | Metastasis | Lung cancer, Non-small cell | Risk factors
antiangiogenic therapy | fibroblast growth factor | NSCLC | angiogenesis | vascular endothelial growth factor | platelet‐derived growth factor | biomarker | platelet-derived growth factor | TARGETED THERAPY | COLLAGEN-XVIII | MICROVESSEL DENSITY | TUMOR ANGIOGENESIS | ADHESION MOLECULES | FACTOR RECEPTOR | VEGF MESSENGER-RNA | ONCOLOGY | SERUM-LEVELS | PATIENT SURVIVAL | CLINICAL-SIGNIFICANCE | Lung Neoplasms - drug therapy | Prognosis | Biomarkers, Tumor - analysis | Carcinoma, Non-Small-Cell Lung - blood supply | Humans | Carcinoma, Non-Small-Cell Lung - metabolism | Neovascularization, Pathologic | Vascular Endothelial Growth Factor A - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Receptors, Vascular Endothelial Growth Factor - metabolism | Angiogenesis Inhibitors - therapeutic use | Carcinoma, Non-Small-Cell Lung - drug therapy | Angiogenic Proteins - metabolism | Lung Neoplasms - blood supply | Care and treatment | Lung cancer | Physiological aspects | Causes of | Neovascularization | Research | Metastasis | Lung cancer, Non-small cell | Risk factors
Journal Article
Current Oncology Reports, ISSN 1523-3790, 1/2007, Volume 9, Issue 2, pp. 102 - 108
Receptor tyrosine kinases have come to fruition as therapeutic targets in a variety of malignancies. In this group of targets, the c-Met receptor tyrosine...
Medicine & Public Health | Oncology | Neoplasms - metabolism | Neoplasms - therapy | Proto-Oncogene Proteins c-met - physiology | Animals | Proto-Oncogene Proteins c-met - antagonists & inhibitors | Humans | Antineoplastic Agents - therapeutic use | Hepatocyte Growth Factor - metabolism
Medicine & Public Health | Oncology | Neoplasms - metabolism | Neoplasms - therapy | Proto-Oncogene Proteins c-met - physiology | Animals | Proto-Oncogene Proteins c-met - antagonists & inhibitors | Humans | Antineoplastic Agents - therapeutic use | Hepatocyte Growth Factor - metabolism
Journal Article
Cancer Medicine, ISSN 2045-7634, 06/2014, Volume 3, Issue 3, pp. 681 - 692
With the introduction of targeted agents primarily applicable to non‐small cell lung cancer (NSCLC) of adenocarcinoma histology, there is a heightened unmet...
fibroblast growth factors | Angiogenesis inhibitors | non‐small cell lung cancer | squamous cell carcinoma | non-small cell lung cancer | GENE-MUTATIONS | BLADDER-CANCER | PROGNOSTIC IMPACT | SOMATIC MUTATIONS | PHASE-II TRIAL | RECEPTOR TYROSINE KINASES | ONCOLOGY | MULTIPLE-MYELOMA PATIENTS | PROSTATE-CANCER | ANGIOGENESIS INHIBITOR | FGFR3 MUTATIONS | Carcinoma, Non-Small-Cell Lung - pathology | Signal Transduction | Carcinoma, Non-Small-Cell Lung - genetics | Humans | Receptors, Fibroblast Growth Factor - antagonists & inhibitors | Fibroblast Growth Factors - genetics | Clinical Trials as Topic | Molecular Targeted Therapy | Indoles - administration & dosage | Neovascularization, Pathologic - pathology | Neoplasms, Squamous Cell - genetics | Neovascularization, Pathologic - drug therapy | Neoplasms, Squamous Cell - drug therapy | Receptors, Fibroblast Growth Factor - genetics | Neovascularization, Pathologic - genetics | Carcinoma, Non-Small-Cell Lung - drug therapy | Fibroblast Growth Factors - antagonists & inhibitors | Neoplasms, Squamous Cell - pathology | Lung cancer, Small cell | Squamous cell carcinoma | Fibroblast growth factors | Lung cancer, Non-small cell | Tumors | Adenocarcinoma | Fibroblast growth factor | Gemcitabine | Lung cancer | Clinical trials | Kinases | Cancer therapies | Proteins | Angiogenesis | Signal transduction | Fibroblasts | Growth factors | Protein-tyrosine kinase | Heparan sulfate | Tyrosine | Non-small cell lung carcinoma | Histology | Cisplatin | Gene amplification | Chemotherapy | Ligands | Mutation | Fibroblast growth factor receptors | Original Research
fibroblast growth factors | Angiogenesis inhibitors | non‐small cell lung cancer | squamous cell carcinoma | non-small cell lung cancer | GENE-MUTATIONS | BLADDER-CANCER | PROGNOSTIC IMPACT | SOMATIC MUTATIONS | PHASE-II TRIAL | RECEPTOR TYROSINE KINASES | ONCOLOGY | MULTIPLE-MYELOMA PATIENTS | PROSTATE-CANCER | ANGIOGENESIS INHIBITOR | FGFR3 MUTATIONS | Carcinoma, Non-Small-Cell Lung - pathology | Signal Transduction | Carcinoma, Non-Small-Cell Lung - genetics | Humans | Receptors, Fibroblast Growth Factor - antagonists & inhibitors | Fibroblast Growth Factors - genetics | Clinical Trials as Topic | Molecular Targeted Therapy | Indoles - administration & dosage | Neovascularization, Pathologic - pathology | Neoplasms, Squamous Cell - genetics | Neovascularization, Pathologic - drug therapy | Neoplasms, Squamous Cell - drug therapy | Receptors, Fibroblast Growth Factor - genetics | Neovascularization, Pathologic - genetics | Carcinoma, Non-Small-Cell Lung - drug therapy | Fibroblast Growth Factors - antagonists & inhibitors | Neoplasms, Squamous Cell - pathology | Lung cancer, Small cell | Squamous cell carcinoma | Fibroblast growth factors | Lung cancer, Non-small cell | Tumors | Adenocarcinoma | Fibroblast growth factor | Gemcitabine | Lung cancer | Clinical trials | Kinases | Cancer therapies | Proteins | Angiogenesis | Signal transduction | Fibroblasts | Growth factors | Protein-tyrosine kinase | Heparan sulfate | Tyrosine | Non-small cell lung carcinoma | Histology | Cisplatin | Gene amplification | Chemotherapy | Ligands | Mutation | Fibroblast growth factor receptors | Original Research
Journal Article
Cancer Letters, ISSN 0304-3835, 04/2019, Volume 447, pp. 24 - 32
Breast tumor metastasis is a leading cause of cancer-related deaths worldwide. Breast cancer (BC) cells frequently metastasize to the lungs, where they pose a...
Breast cancer | Chemotherapeutics | Phytochemicals | Metastasis | Lung | RLIP | REGRESSION | FLAVANONE | CANCER CELLS | 2'-HYDROXYFLAVANONE | CELL-CYCLE ARREST | PROLIFERATION | INDUCTION | TRANSPORT | ONCOLOGY | TUMOR-GROWTH | EXPRESSION | Viral antibodies | Antibodies | Evaluation | Cellular signal transduction | Progesterone | Estrogen | Phosphorylation | Motility | Antisense | Metastases | Proteins | Angiogenesis | Cell cycle | Inhibition | Citrus fruits | Immunoglobulins | Invasiveness | Studies | Depletion | Lungs | Cell lines | Weight reduction | Breast | Protein expression | Mice | Prostate | Viability | Cancer | Tumors
Breast cancer | Chemotherapeutics | Phytochemicals | Metastasis | Lung | RLIP | REGRESSION | FLAVANONE | CANCER CELLS | 2'-HYDROXYFLAVANONE | CELL-CYCLE ARREST | PROLIFERATION | INDUCTION | TRANSPORT | ONCOLOGY | TUMOR-GROWTH | EXPRESSION | Viral antibodies | Antibodies | Evaluation | Cellular signal transduction | Progesterone | Estrogen | Phosphorylation | Motility | Antisense | Metastases | Proteins | Angiogenesis | Cell cycle | Inhibition | Citrus fruits | Immunoglobulins | Invasiveness | Studies | Depletion | Lungs | Cell lines | Weight reduction | Breast | Protein expression | Mice | Prostate | Viability | Cancer | Tumors
Journal Article
Cancer Letters, ISSN 0304-3835, 12/2018, Volume 438, pp. 144 - 153
Brain metastasis is an important cause of morbidity and mortality in cancer-patients. Breast tumor cells frequently metastasize to brain and initiate severe...
Breast cancer | Chemotherapeutics | Phytochemicals | Brain metastasis | RLIP | GLUTATHIONE-CONJUGATE | PROLIFERATION | LUNG-CANCER CELLS | EFFECTOR | TRANSPORT | ONCOLOGY | RAL PATHWAY | EXPRESSION | GTPASE | ENDOTHELIAL GROWTH-FACTOR | Heart | Evaluation | Health aspects | Brain tumors | Imaging systems | Neuroimaging | Brain | Animal models | Clinical trials | Metastasis | Kinases | Cancer therapies | Metastases | Fruits | Angiogenesis | Cell cycle | Vascular endothelial growth factor | Immunoglobulins | Medical imaging | Complications | Tumor cells | Invasiveness | Morbidity | Studies | Brain research | Breast | Mice | Ventricle | Prostate | Cell migration | Cancer | Apoptosis | Tumors
Breast cancer | Chemotherapeutics | Phytochemicals | Brain metastasis | RLIP | GLUTATHIONE-CONJUGATE | PROLIFERATION | LUNG-CANCER CELLS | EFFECTOR | TRANSPORT | ONCOLOGY | RAL PATHWAY | EXPRESSION | GTPASE | ENDOTHELIAL GROWTH-FACTOR | Heart | Evaluation | Health aspects | Brain tumors | Imaging systems | Neuroimaging | Brain | Animal models | Clinical trials | Metastasis | Kinases | Cancer therapies | Metastases | Fruits | Angiogenesis | Cell cycle | Vascular endothelial growth factor | Immunoglobulins | Medical imaging | Complications | Tumor cells | Invasiveness | Morbidity | Studies | Brain research | Breast | Mice | Ventricle | Prostate | Cell migration | Cancer | Apoptosis | Tumors
Journal Article