Nature Nanotechnology, ISSN 1748-3387, 2012, Volume 7, Issue 6, pp. 383 - 388
The blood vessels of cancerous tumours are leaky(1-3) and poorly organized(4-7). This can increase the interstitial fluid pressure inside tumours and reduce...
VASCULAR NORMALIZATION | ANTIANGIOGENIC THERAPY | TRANSPORT | SOLID TUMORS | FLUID-FLOW | ANGIOGENESIS | MATERIALS SCIENCE, MULTIDISCIPLINARY | GROWTH | PENETRATION | NANOSCIENCE & NANOTECHNOLOGY | CANCER | GLIOBLASTOMA PATIENTS | Angiogenesis Inhibitors - pharmacology | Mammary Neoplasms, Experimental - physiopathology | Mammary Neoplasms, Experimental - metabolism | Mice, SCID | Nanoparticles | Animals | Receptors, Vascular Endothelial Growth Factor - metabolism | Nanomedicine - methods | Mammary Neoplasms, Experimental - pathology | Receptors, Vascular Endothelial Growth Factor - antagonists & inhibitors | Female | Mammary Neoplasms, Experimental - blood supply | Mice | Drug Delivery Systems - methods | Mammary Neoplasms, Experimental - drug therapy
VASCULAR NORMALIZATION | ANTIANGIOGENIC THERAPY | TRANSPORT | SOLID TUMORS | FLUID-FLOW | ANGIOGENESIS | MATERIALS SCIENCE, MULTIDISCIPLINARY | GROWTH | PENETRATION | NANOSCIENCE & NANOTECHNOLOGY | CANCER | GLIOBLASTOMA PATIENTS | Angiogenesis Inhibitors - pharmacology | Mammary Neoplasms, Experimental - physiopathology | Mammary Neoplasms, Experimental - metabolism | Mice, SCID | Nanoparticles | Animals | Receptors, Vascular Endothelial Growth Factor - metabolism | Nanomedicine - methods | Mammary Neoplasms, Experimental - pathology | Receptors, Vascular Endothelial Growth Factor - antagonists & inhibitors | Female | Mammary Neoplasms, Experimental - blood supply | Mice | Drug Delivery Systems - methods | Mammary Neoplasms, Experimental - drug therapy
Journal Article
Nature Communications, ISSN 2041-1723, 2013, Volume 4, Issue 1, p. 2516
Cancer and stromal cells actively exert physical forces (solid stress) to compress tumour blood vessels, thus reducing vascular perfusion. Tumour interstitial...
INTERSTITIAL FLUID PRESSURE | BREAST-CANCER | GROWTH-FACTOR-BETA | PANCREATIC STELLATE CELLS | TGF-BETA | AORTIC-ANEURYSM | SOLID STRESS | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | GENE-EXPRESSION | II TYPE-2 RECEPTOR
INTERSTITIAL FLUID PRESSURE | BREAST-CANCER | GROWTH-FACTOR-BETA | PANCREATIC STELLATE CELLS | TGF-BETA | AORTIC-ANEURYSM | SOLID STRESS | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | GENE-EXPRESSION | II TYPE-2 RECEPTOR
Journal Article
Cancer Cell, ISSN 1535-6108, 2011, Volume 19, Issue 4, pp. 512 - 526
Tumor-infiltrating myeloid cells convey proangiogenic programs that counteract the efficacy of antiangiogenic therapy. Here, we show that blocking...
ONCOLOGY | PATHWAY | VASCULATURE | TIE2-EXPRESSING MONOCYTES | RESISTANCE | ANGIOPOIETIN-2 | EXPRESSION | CANCER | PROGRESSION | DELIVERY | BLOOD | CELL BIOLOGY | Macrophages - physiology | Mammary Neoplasms, Experimental - prevention & control | Receptor, TIE-2 | Humans | Mice, Inbred C57BL | Myeloid Cells - physiology | Receptor Protein-Tyrosine Kinases - physiology | Gene Expression Regulation, Neoplastic | Neoplasms, Experimental - prevention & control | Cell Communication | Animals | Neoplasm Metastasis - prevention & control | Mammary Neoplasms, Experimental - pathology | Angiopoietin-2 - physiology | Neuroendocrine Tumors - prevention & control | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Mammary Neoplasms, Experimental - blood supply | Neovascularization, Pathologic - prevention & control | Mice | Angiopoietin-2 - antagonists & inhibitors | Endothelial Cells - physiology | Neoplasms, Experimental - blood supply | Development and progression | Care and treatment | Metastasis | Analysis | Stem cells | Cancer
ONCOLOGY | PATHWAY | VASCULATURE | TIE2-EXPRESSING MONOCYTES | RESISTANCE | ANGIOPOIETIN-2 | EXPRESSION | CANCER | PROGRESSION | DELIVERY | BLOOD | CELL BIOLOGY | Macrophages - physiology | Mammary Neoplasms, Experimental - prevention & control | Receptor, TIE-2 | Humans | Mice, Inbred C57BL | Myeloid Cells - physiology | Receptor Protein-Tyrosine Kinases - physiology | Gene Expression Regulation, Neoplastic | Neoplasms, Experimental - prevention & control | Cell Communication | Animals | Neoplasm Metastasis - prevention & control | Mammary Neoplasms, Experimental - pathology | Angiopoietin-2 - physiology | Neuroendocrine Tumors - prevention & control | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Mammary Neoplasms, Experimental - blood supply | Neovascularization, Pathologic - prevention & control | Mice | Angiopoietin-2 - antagonists & inhibitors | Endothelial Cells - physiology | Neoplasms, Experimental - blood supply | Development and progression | Care and treatment | Metastasis | Analysis | Stem cells | Cancer
Journal Article
1979, ISBN 0849356954, 229
Book
The New England Journal of Medicine, ISSN 0028-4793, 10/2010, Volume 363, Issue 17, pp. 1621 - 1630
This study showed near-universal expression of FSH receptors on a subgroup of tumor-vessel endothelial cells in a band near the outer edge of tumors where they...
BREAST-CANCER | LOCALIZATION | MEDICINE, GENERAL & INTERNAL | PROSTATE-CANCER | CARCINOMAS | CELL-PROLIFERATION | FSH | PROTEINS | Endothelial Cells - chemistry | Prostatic Neoplasms - blood supply | Neoplasm Transplantation | Prostatic Neoplasms - chemistry | Blood Vessels - chemistry | Immunologic Techniques | Receptors, FSH - immunology | Electrophoresis, Polyacrylamide Gel | Humans | Male | Neoplasms - blood supply | Transplantation, Heterologous | Microscopy, Immunoelectron | Neoplasms - chemistry | Animals | In Situ Hybridization | Antibodies, Monoclonal - analysis | Neoplasms, Experimental - chemistry | Mice | Disease Models, Animal | Neoplasms, Experimental - blood supply | Receptors, FSH - analysis | Care and treatment | Follicle-stimulating hormone | Blood-vessels | Analysis | Physiological aspects | Genetic aspects | Gene expression | Health aspects | Cancer | Tumors | Proteins | Microscopy | Rodents | Surgery
BREAST-CANCER | LOCALIZATION | MEDICINE, GENERAL & INTERNAL | PROSTATE-CANCER | CARCINOMAS | CELL-PROLIFERATION | FSH | PROTEINS | Endothelial Cells - chemistry | Prostatic Neoplasms - blood supply | Neoplasm Transplantation | Prostatic Neoplasms - chemistry | Blood Vessels - chemistry | Immunologic Techniques | Receptors, FSH - immunology | Electrophoresis, Polyacrylamide Gel | Humans | Male | Neoplasms - blood supply | Transplantation, Heterologous | Microscopy, Immunoelectron | Neoplasms - chemistry | Animals | In Situ Hybridization | Antibodies, Monoclonal - analysis | Neoplasms, Experimental - chemistry | Mice | Disease Models, Animal | Neoplasms, Experimental - blood supply | Receptors, FSH - analysis | Care and treatment | Follicle-stimulating hormone | Blood-vessels | Analysis | Physiological aspects | Genetic aspects | Gene expression | Health aspects | Cancer | Tumors | Proteins | Microscopy | Rodents | Surgery
Journal Article
British Journal of Haematology, ISSN 0007-1048, 08/2013, Volume 162, Issue 4, pp. 433 - 441
Summary Inhibition of coagulation greatly limits cancer metastasis in many experimental models. Cancer cells trigger coagulation, through expression of tissue...
aspirin | macrophages | tissue factor | metastasis | coagulation | Aspirin | Metastasis | Macrophages | Coagulation | Tissue factor | CANCER-CELLS | RANDOMIZED CONTROLLED-TRIALS | EXPERIMENTAL MELANOMA METASTASIS | COLORECTAL-CANCER | HEMATOGENOUS METASTASIS | TUMOR-METASTASIS | ENDOTHELIAL-CELLS | P-SELECTIN | HEMATOLOGY | THROMBIN INHIBITOR | Thrombin - secretion | Humans | Neoplasm Proteins - physiology | Neuraminidase - therapeutic use | Platelet Activation - physiology | Blood Platelets - physiology | Cytoplasmic Granules - secretion | Cysteine Endopeptidases - physiology | Thrombophilia - complications | Thromboplastin - physiology | Neoplasms, Experimental - pathology | Lung Neoplasms - secondary | Neoplasm Metastasis - drug therapy | Neoplasm Metastasis - prevention & control | Killer Cells, Natural - immunology | Platelet Aggregation Inhibitors - pharmacology | Blood Platelets - drug effects | Platelet Aggregation Inhibitors - therapeutic use | Macrophages - immunology | Thrombophilia - drug therapy | Rats | Anticoagulants - therapeutic use | P-Selectin - physiology | Neuraminidase - pharmacology | Animals | Blood Coagulation - drug effects | Lung Neoplasms - prevention & control | Anticoagulants - pharmacology | Neoplasm Metastasis - physiopathology | Neoplastic Cells, Circulating | Mice | Hirudins - pharmacology | Neoplasms, Experimental - blood | Neoplasms, Experimental - blood supply | Thrombin
aspirin | macrophages | tissue factor | metastasis | coagulation | Aspirin | Metastasis | Macrophages | Coagulation | Tissue factor | CANCER-CELLS | RANDOMIZED CONTROLLED-TRIALS | EXPERIMENTAL MELANOMA METASTASIS | COLORECTAL-CANCER | HEMATOGENOUS METASTASIS | TUMOR-METASTASIS | ENDOTHELIAL-CELLS | P-SELECTIN | HEMATOLOGY | THROMBIN INHIBITOR | Thrombin - secretion | Humans | Neoplasm Proteins - physiology | Neuraminidase - therapeutic use | Platelet Activation - physiology | Blood Platelets - physiology | Cytoplasmic Granules - secretion | Cysteine Endopeptidases - physiology | Thrombophilia - complications | Thromboplastin - physiology | Neoplasms, Experimental - pathology | Lung Neoplasms - secondary | Neoplasm Metastasis - drug therapy | Neoplasm Metastasis - prevention & control | Killer Cells, Natural - immunology | Platelet Aggregation Inhibitors - pharmacology | Blood Platelets - drug effects | Platelet Aggregation Inhibitors - therapeutic use | Macrophages - immunology | Thrombophilia - drug therapy | Rats | Anticoagulants - therapeutic use | P-Selectin - physiology | Neuraminidase - pharmacology | Animals | Blood Coagulation - drug effects | Lung Neoplasms - prevention & control | Anticoagulants - pharmacology | Neoplasm Metastasis - physiopathology | Neoplastic Cells, Circulating | Mice | Hirudins - pharmacology | Neoplasms, Experimental - blood | Neoplasms, Experimental - blood supply | Thrombin
Journal Article
Cancer Research, ISSN 0008-5472, 01/2010, Volume 70, Issue 2, pp. 741 - 751
Epidemiologic studies suggest that type 2 diabetes (T2D) increases breast cancer risk and mortality, but there is limited experimental evidence supporting this...
SIGNALING PATHWAYS | METABOLIC SYNDROME | IGF-I | METAANALYSIS | ONCOLOGY | TRANSGENIC MOUSE | 7,12-DIMETHYLBENZ(A)ANTHRACENE-INDUCED MAMMARY-CARCINOMA | RECEPTOR | MICE | CELL-LINES | GROWTH-FACTOR-I | Receptor, IGF Type 1 - metabolism | Phosphorylation | Receptor, IGF Type 1 - antagonists & inhibitors | Phosphatidylinositol 3-Kinases - metabolism | Diabetes Mellitus, Type 2 - metabolism | Insulin - blood | Mammary Neoplasms, Experimental - metabolism | Diabetes Mellitus, Experimental - blood | Mammary Glands, Animal - growth & development | Mammary Neoplasms, Experimental - pathology | Female | Diabetes Mellitus, Experimental - metabolism | Oncogene Protein v-akt - metabolism | Hyperinsulinism - blood | Diabetes Mellitus, Type 2 - complications | Disease Models, Animal | Hyperinsulinism - metabolism | Mice, Transgenic | Receptor, Insulin - antagonists & inhibitors | Mammary Neoplasms, Experimental - blood | Hyperinsulinism - pathology | Diabetes Mellitus, Type 2 - blood | Animals | Mammary Glands, Animal - metabolism | Benzimidazoles - pharmacology | Receptor, Insulin - metabolism | Mice | Diabetes Mellitus, Type 2 - pathology | Mammary Neoplasms, Experimental - etiology | Pyridones - pharmacology | Index Medicus
SIGNALING PATHWAYS | METABOLIC SYNDROME | IGF-I | METAANALYSIS | ONCOLOGY | TRANSGENIC MOUSE | 7,12-DIMETHYLBENZ(A)ANTHRACENE-INDUCED MAMMARY-CARCINOMA | RECEPTOR | MICE | CELL-LINES | GROWTH-FACTOR-I | Receptor, IGF Type 1 - metabolism | Phosphorylation | Receptor, IGF Type 1 - antagonists & inhibitors | Phosphatidylinositol 3-Kinases - metabolism | Diabetes Mellitus, Type 2 - metabolism | Insulin - blood | Mammary Neoplasms, Experimental - metabolism | Diabetes Mellitus, Experimental - blood | Mammary Glands, Animal - growth & development | Mammary Neoplasms, Experimental - pathology | Female | Diabetes Mellitus, Experimental - metabolism | Oncogene Protein v-akt - metabolism | Hyperinsulinism - blood | Diabetes Mellitus, Type 2 - complications | Disease Models, Animal | Hyperinsulinism - metabolism | Mice, Transgenic | Receptor, Insulin - antagonists & inhibitors | Mammary Neoplasms, Experimental - blood | Hyperinsulinism - pathology | Diabetes Mellitus, Type 2 - blood | Animals | Mammary Glands, Animal - metabolism | Benzimidazoles - pharmacology | Receptor, Insulin - metabolism | Mice | Diabetes Mellitus, Type 2 - pathology | Mammary Neoplasms, Experimental - etiology | Pyridones - pharmacology | Index Medicus
Journal Article
Clinical & Experimental Metastasis, ISSN 0262-0898, 10/2018, Volume 35, Issue 7, pp. 679 - 689
Platelets are thought to play an important role in metastasis formation, although the mechanisms involved remain incompletely understood. Here we studied the...
Biomedicine, general | Tpo deficient mice | Biomedicine | Hematology | Lymph node | Tumor growth | Cancer Research | Oncology | Metastasis | Platelets | Surgical Oncology | CANCER-CELLS | VIVO | TRANSENDOTHELIAL MIGRATION | HEMATOGENOUS-METASTASIS | MODEL | PULMONARY METASTASES | ONCOLOGY | LYMPH-NODE | BLOOD-VESSELS | INTERACTION IN-VITRO | TISSUE FACTOR | Blood Platelets - pathology | Lung Neoplasms - genetics | Lymphatic Metastasis | Mammary Neoplasms, Experimental - blood | Mammary Neoplasms, Experimental - genetics | Thromboplastin - deficiency | Neoplasm Metastasis | Animals | Lung Neoplasms - secondary | Blood Platelets - metabolism | Thromboplastin - genetics | Mammary Neoplasms, Experimental - pathology | Cell Line, Tumor | Female | Lung Neoplasms - blood | Mice | Mice, Inbred BALB C | Lymphatic system | Olefinic thermoplastic elastomers | Breast cancer | Lymph nodes | Metastases | Lungs | Breast | Tumors | Cancer | Lymph
Biomedicine, general | Tpo deficient mice | Biomedicine | Hematology | Lymph node | Tumor growth | Cancer Research | Oncology | Metastasis | Platelets | Surgical Oncology | CANCER-CELLS | VIVO | TRANSENDOTHELIAL MIGRATION | HEMATOGENOUS-METASTASIS | MODEL | PULMONARY METASTASES | ONCOLOGY | LYMPH-NODE | BLOOD-VESSELS | INTERACTION IN-VITRO | TISSUE FACTOR | Blood Platelets - pathology | Lung Neoplasms - genetics | Lymphatic Metastasis | Mammary Neoplasms, Experimental - blood | Mammary Neoplasms, Experimental - genetics | Thromboplastin - deficiency | Neoplasm Metastasis | Animals | Lung Neoplasms - secondary | Blood Platelets - metabolism | Thromboplastin - genetics | Mammary Neoplasms, Experimental - pathology | Cell Line, Tumor | Female | Lung Neoplasms - blood | Mice | Mice, Inbred BALB C | Lymphatic system | Olefinic thermoplastic elastomers | Breast cancer | Lymph nodes | Metastases | Lungs | Breast | Tumors | Cancer | Lymph
Journal Article
Genes and Development, ISSN 0890-9369, 06/2007, Volume 21, Issue 12, pp. 1546 - 1558
Tumors build vessels by cooption of pre-existing vasculature and de novo recruitment of bone marrow (BM)-derived endothelial progenitor cells (EPCs). However,...
Bone marrow transplantation | Tumor angiogenesis | Neovascularization | Endothelial cells | Endothelial progenitor cells | VE-cadherin | endothelial cells | ANGIOGENIC SWITCH | neovascularization | DEVELOPMENTAL BIOLOGY | CANCER | bone marrow transplantation | CELL BIOLOGY | MAMMARY-TUMORS | THERAPY | endothelial progenitor cells | VASCULATURE | tumor angiogenesis | HEMATOPOIETIC STEM-CELLS | MOUSE MODEL | IN-VIVO | GENETICS & HEREDITY | BLOOD-VESSELS | Mice, Inbred C57BL | Neovascularization, Pathologic | Hematopoietic Stem Cells - pathology | Male | Mice, Transgenic | Mammary Neoplasms, Experimental - genetics | Neoplasms, Experimental - pathology | Animals | Mammary Neoplasms, Experimental - pathology | Neoplasms, Experimental - genetics | Cell Line, Tumor | Female | Mammary Neoplasms, Experimental - blood supply | Cell Differentiation | Mice | Endothelial Cells - pathology | Neoplasms, Experimental - blood supply | Bone marrow cells | Research | Cancer cells | Endothelium | Research Paper
Bone marrow transplantation | Tumor angiogenesis | Neovascularization | Endothelial cells | Endothelial progenitor cells | VE-cadherin | endothelial cells | ANGIOGENIC SWITCH | neovascularization | DEVELOPMENTAL BIOLOGY | CANCER | bone marrow transplantation | CELL BIOLOGY | MAMMARY-TUMORS | THERAPY | endothelial progenitor cells | VASCULATURE | tumor angiogenesis | HEMATOPOIETIC STEM-CELLS | MOUSE MODEL | IN-VIVO | GENETICS & HEREDITY | BLOOD-VESSELS | Mice, Inbred C57BL | Neovascularization, Pathologic | Hematopoietic Stem Cells - pathology | Male | Mice, Transgenic | Mammary Neoplasms, Experimental - genetics | Neoplasms, Experimental - pathology | Animals | Mammary Neoplasms, Experimental - pathology | Neoplasms, Experimental - genetics | Cell Line, Tumor | Female | Mammary Neoplasms, Experimental - blood supply | Cell Differentiation | Mice | Endothelial Cells - pathology | Neoplasms, Experimental - blood supply | Bone marrow cells | Research | Cancer cells | Endothelium | Research Paper
Journal Article
Cancer Research, ISSN 0008-5472, 08/2012, Volume 72, Issue 16, pp. 3919 - 3927
Although circulating neutrophils are associated with distant metastasis and poor outcome in a number of epithelial malignancies, it remains unclear whether...
LYMPHOCYTE RATIO | ADHESION | FLOW CONDITIONS | ONCOLOGY | CANCER METASTASIS | INFLAMMATION | IN-VIVO | PREDICTS SURVIVAL | COMPLICATIONS | RECURRENCE | CARCINOMA | Liver Neoplasms, Experimental - secondary | Neoplastic Cells, Circulating - pathology | Humans | Lung Neoplasms - metabolism | Carcinoma, Lewis Lung - immunology | Neutrophil Activation - drug effects | Cell Communication - physiology | Lung Neoplasms - pathology | Liver Neoplasms, Experimental - immunology | Cell Aggregation - physiology | Liver Neoplasms, Experimental - metabolism | Macrophage-1 Antigen - metabolism | Lung Neoplasms - blood supply | Neutrophils - pathology | Mice, Inbred C57BL | Neutrophils - drug effects | Neutrophils - immunology | Carcinoma, Lewis Lung - blood | Carcinoma, Lewis Lung - metabolism | Liver Neoplasms, Experimental - blood | Mice, Knockout | Microscopy, Confocal | Lung Neoplasms - immunology | Animals | Lipopolysaccharides - pharmacology | Carcinoma, Lewis Lung - pathology | Cell Line, Tumor | Human Umbilical Vein Endothelial Cells - pathology | Mice
LYMPHOCYTE RATIO | ADHESION | FLOW CONDITIONS | ONCOLOGY | CANCER METASTASIS | INFLAMMATION | IN-VIVO | PREDICTS SURVIVAL | COMPLICATIONS | RECURRENCE | CARCINOMA | Liver Neoplasms, Experimental - secondary | Neoplastic Cells, Circulating - pathology | Humans | Lung Neoplasms - metabolism | Carcinoma, Lewis Lung - immunology | Neutrophil Activation - drug effects | Cell Communication - physiology | Lung Neoplasms - pathology | Liver Neoplasms, Experimental - immunology | Cell Aggregation - physiology | Liver Neoplasms, Experimental - metabolism | Macrophage-1 Antigen - metabolism | Lung Neoplasms - blood supply | Neutrophils - pathology | Mice, Inbred C57BL | Neutrophils - drug effects | Neutrophils - immunology | Carcinoma, Lewis Lung - blood | Carcinoma, Lewis Lung - metabolism | Liver Neoplasms, Experimental - blood | Mice, Knockout | Microscopy, Confocal | Lung Neoplasms - immunology | Animals | Lipopolysaccharides - pharmacology | Carcinoma, Lewis Lung - pathology | Cell Line, Tumor | Human Umbilical Vein Endothelial Cells - pathology | Mice
Journal Article
Science, ISSN 0036-8075, 5/2012, Volume 336, Issue 6081, pp. 604 - 608
Medical applications of nanotechnology typically focus on drug delivery and biosensors. Here, we combine nanotechnology and bioengineering to demonstrate that...
Nanoparticles | Blood glucose | Calcium | REPORTS | Gene expression regulation | Gene expression | Insulin | Ferritins | Nanotechnology | Tumors | Blood plasma | HYPERTHERMIA | STIMULATION | PROTEIN | MULTIDISCIPLINARY SCIENCES | FREQUENCY | CALCIUM | GENE-EXPRESSION | NEURONS | FERRITIN | Bioengineering | Embryonic Stem Cells - metabolism | Neoplasm Transplantation | Calcium - metabolism | Humans | Male | Transplantation, Heterologous | Insulin - blood | PC12 Cells | Ferritins - administration & dosage | Neoplasms, Experimental - pathology | TRPV Cation Channels - metabolism | Ferritins - metabolism | Transfection | Ferritins - genetics | HEK293 Cells | Insulin - genetics | Recombinant Fusion Proteins - administration & dosage | Blood Glucose - analysis | TRPV Cation Channels - immunology | Radio Waves | Rats | Epitopes | Hot Temperature | TRPV Cation Channels - genetics | Ferric Compounds | Insulin - metabolism | Animals | Mice, Nude | Mice | Metal Nanoparticles | Neoplasms, Experimental - blood | Thermal properties | Composition | Heating | Atomic properties | Physiological aspects | Research | Glucose | Iron oxides | Health aspects | Dextrose | Plasma | Signal transduction | Rodents | Genes
Nanoparticles | Blood glucose | Calcium | REPORTS | Gene expression regulation | Gene expression | Insulin | Ferritins | Nanotechnology | Tumors | Blood plasma | HYPERTHERMIA | STIMULATION | PROTEIN | MULTIDISCIPLINARY SCIENCES | FREQUENCY | CALCIUM | GENE-EXPRESSION | NEURONS | FERRITIN | Bioengineering | Embryonic Stem Cells - metabolism | Neoplasm Transplantation | Calcium - metabolism | Humans | Male | Transplantation, Heterologous | Insulin - blood | PC12 Cells | Ferritins - administration & dosage | Neoplasms, Experimental - pathology | TRPV Cation Channels - metabolism | Ferritins - metabolism | Transfection | Ferritins - genetics | HEK293 Cells | Insulin - genetics | Recombinant Fusion Proteins - administration & dosage | Blood Glucose - analysis | TRPV Cation Channels - immunology | Radio Waves | Rats | Epitopes | Hot Temperature | TRPV Cation Channels - genetics | Ferric Compounds | Insulin - metabolism | Animals | Mice, Nude | Mice | Metal Nanoparticles | Neoplasms, Experimental - blood | Thermal properties | Composition | Heating | Atomic properties | Physiological aspects | Research | Glucose | Iron oxides | Health aspects | Dextrose | Plasma | Signal transduction | Rodents | Genes
Journal Article