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  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Toxicology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (411 pages)
    Edition: 1st ed.
    ISBN: 9783319413426
    Series Statement: Advances in Experimental Medicine and Biology Series ; v.929
    DDC: 615.794
    Language: English
    Note: Intro -- Contents -- About the Editors -- 1 Cinnamon and Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physiochemical Properties of Cinnamon -- 3 Modulation of Cell Signaling Pathways by Cinnamon -- 4 Role of Cinnamon in Chronic Diseases -- 4.1 Cinnamon Used to Reduce Blood Sugar in Diabetics -- 4.2 Cinnamon for Arthritis and Pain Relief -- 4.3 Cinnamon and Heart Disease -- 4.4 Cinnamon and Alzheimer's Disease -- 5 Anti-inflammatory Effects of Cinnamon in Allergies -- 6 Anti-inflammatory Effect of Cinnamon on Colitis -- 7 Anti-inflammatory Effects of Cinnamon on Helicobacter pylori-induced Gastritis -- 8 Biological Activity of Cinnamon in Human -- 9 Biological Activity of Cinnamon in Animals -- 10 How Much Cinnamon Can Be Consumed Per Day -- 11 Conclusion -- References -- 2 Silymarin and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physicochemical Properties of Silymarin -- 3 Modulation of Cell Signaling Pathways by Silymarin -- 4 Role of Silymarin in Chronic Diseases -- 5 Biological Activities of Silymarin in Animal Models -- 6 Biological Activities of Silymarin in Humans -- 7 Conclusion -- References -- 3 Eugenol and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physicochemical Properties of Eugenol -- 2.1 Chemistry and Metabolites -- 2.2 Antioxidant Activity (Stoichiometric Factor N and Kinh/Kp) -- 2.3 Theoretical Parameters (BDE and IP) Versus Kinh/Kp -- 3 Modulation of Cell Signaling Pathways by Eugenol -- 3.1 Anti-proliferative Activity -- 3.2 Cox-2 Inhibition -- 4 Role of Eugenol in Chronic Diseases -- 5 Biological Activities of Eugenol in Animal Models -- 6 Biological Activities of Eugenol in Humans -- 7 Conclusions -- Acknowledgments -- References -- 4 Catechins and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physicochemical Properties of Catechins. , 3 Modulation of Cell Signaling Pathways by Catechins -- 4 Biological Activities of Catechins in Animal Models -- 5 Biological Activities of Catechins in Humans -- 6 Conclusions -- References -- 5 Capsaicin and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 1.1 Physico-Chemical Properties of Capsaicin -- 1.1.1 Activities and Modulation of Cell Signalling Pathways by Capsaicin -- 1.1.2 Capsaicin Effects on Neuronal and Non-neuronal Cells -- 1.1.3 Do Capsaicin and Its TRPV1 Receptor Represent a Target for Multiple Chronic Diseases Therapy? -- 1.1.4 Effects of Capsaicin on Arthritis -- 1.1.5 Management of Chronic Pain by Capsaicin -- 1.2 Effects of Capsaicin on Functional Gastrointestinal Disorders -- 1.3 Capsaicin and Cancer -- 1.4 Capsaicin and Asthma -- 2 Conclusive Remark and Future Direction -- References -- 6 Diallyl Sulfide and Its Role in Chronic Diseases Prevention -- Abstract -- 1 Introduction -- 2 Diallyl Sulfide as an Important Ingredient of Garlic -- 3 Physiochemical Properties of Diallyl Sulfide -- 4 Modulation of Cell Signaling Pathways by Diallyl Sulfide -- 4.1 Cell Cycle-Associated Pathways -- 4.2 Cellular Mechanistic Pathways -- 4.3 Inflammatory Pathways -- 5 Protective Effects of Diallyl Sulfide in Various Diseases -- 5.1 Neuronal Diseases -- 5.2 Cancer Chemoprevention and Chemotherapeutic Properties -- 5.3 Diabetes and Cardiovascular Diseases -- 5.4 Lung Diseases -- 5.5 Intestinal Disease -- 5.6 Hepatotoxicity and Liver Diseases -- 6 Biological Activities of Diallyl Sulfide in Animal Models -- 6.1 Antioxidant Activity -- 6.2 Antigenotoxic Potential -- 6.3 Immunostimulation -- 6.4 Antibacterial Activity -- 6.5 Anticarcinogenic Effects -- 7 Conclusions -- References -- 7 Lupeol and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physio-chemical Properties of Lupeol. , 3 Modulation of Cell Signaling Pathways by Lupeol -- 3.1 Cell Signaling Pathways of Anti-inflammatory Mechanism -- 3.2 Cell Signaling Pathways of Hepatoprotective Effects -- 3.3 Cell Signaling Pathways of Anticancer Effects -- 4 Role of Lupeol in Various Chronic Diseases -- 4.1 Oxidative Stress-Related Disorders -- 4.2 Inflammatory Disorders Including Arthritis, Asthma and Wound -- 4.3 Cardiovascular Disorders -- 4.4 Hepatic Injury -- 4.5 Urolithiasis and Renal Disorders -- 4.6 Pancreatitis -- 4.7 Diabetic Mellitus and Dyslipidemia -- 4.8 Neurodegenerative Disorders -- 4.9 Mutagenesis and Cancer -- 5 Biological Activities of Lupeol in Humans -- 6 Conclusions -- References -- 8 Gingerol and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physico-chemical Properties of Gingerol -- 2.1 Pharmacokinetic of [6]-Gingerol and its Metabolism -- 2.2 Biosynthesis of Gingerols -- 3 Modulation of Cell Signaling Pathways by Gingerol -- 3.1 MAPK -- 3.2 ERK/RAS/RAF -- 3.3 NF-κB/COX2 -- 3.4 AP-1 -- 3.5 PI3K/AKT -- 3.6 β-Catenin/Wnt Pathway -- 3.7 Cell Cycle -- 3.8 Apoptosis -- 3.9 Tumor Suppressor Gene P53 -- 3.10 mTOR -- 4 Role of Gingerol in Chronic Diseases -- 4.1 Role of Gingerol in Cancer -- 4.1.1 Skin Cancer -- 4.1.2 Brain Cancer -- 4.1.3 Gastrointestinal Cancer -- 4.1.4 Liver Cancer -- 4.1.5 Pancreatic Cancer -- 4.1.6 Colon Cancer -- 4.2 Coronary Heart Disease -- 4.3 Asthma -- 4.4 Diabetes -- 5 Biological Activities of Gingerol -- 5.1 In Vitro Biological Activities of Gingerol -- 5.1.1 Antioxidant Activity -- 5.1.2 Anticancer Activity -- 5.1.3 Anti-inflammatory Activity -- 5.1.4 Anti-angiogenesis, Anti-invasion and Metastasis Activity -- 5.1.5 Anti-microbial and Anti-fungal Activity -- 5.1.6 Neuroprotective Activity -- 5.2 In Vivo Biological Activity of Gingerol: Anticancer Property -- 5.2.1 Colon Carcinogenesis -- 5.2.2 Skin Carcinogenesis. , 5.2.3 Liver Carcinogenesis -- 6 Biological Activities of Gingerol in Humans -- 6.1 Anti-emetic Effect -- 6.2 Anticancer Effect -- 6.3 Lipid-Lowering Effect -- 7 Conclusion -- References -- 9 Potential Use of Flavopiridol in Treatment of Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physio-chemical Properties of Flavopiridol -- 3 Modulation of Cell Signaling Pathways by Flavopiridol -- 4 Role of Flavopiridol in Chronic Diseases -- 4.1 Flavopiridol and Hematologic Malignancies -- 4.1.1 Chronic Lymphocytic Leukemia -- 4.1.2 Other Hematologic Neoplasms -- 4.2 Flavopiridol and Its Role in Solid Tumors -- 4.2.1 Sarcoma -- 4.2.2 Breast Cancer -- 4.2.3 Colon Cancer -- 4.2.4 Pancreatic Cancer -- 4.3 Flavopiridol in Neurological Disorders -- 4.3.1 Neurodegenerative Diseases -- 4.3.2 Stroke -- 4.3.3 Traumatic Brain Injury -- 4.4 Flavopiridol in Cardiovascular Disease -- 4.5 Flavopiridol in Infectious Disease -- 4.5.1 Human Immunodeficiency Virus-1 (HIV-1) -- 4.5.2 Human Herpes Simplex Virus 1 (HSV-1) -- 5 Conclusions -- Acknowledgments -- References -- 10 Plumbagin and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physicochemical Properties of Plumbagin -- 3 Modulation of Cell Signaling Pathways by Plumbagin -- 4 Role of Plumbagin in Chronic Diseases -- 4.1 Cancer Diseases -- 4.2 Cardiovascular Diseases -- 4.3 Diabetes Mellitus -- 4.4 Infectious Diseases -- 5 Other Pharmacological Activity of Plumbagin -- 6 Toxicity Assessment of Plumbagin -- 7 Conclusions -- 11 Anethole and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Physicochemical Properties of Anethole -- 3 Pharmacokinetic Profile of Anethole -- 4 Modulation of Cell Signaling Pathways by Anethole -- 5 Role of Anethole in Chronic Diseases -- 5.1 Anethole and Inflammatory Process -- 5.2 Anethole and Cancer -- 5.3 Anethole and Diabetes. , 5.4 Anethole and Neurological Diseases -- 6 Biological Activities of Anethole in Animal Models -- 6.1 Anti-inflammatory and Antihypernociceptive Activities -- 6.2 Immunomodulatory Activity -- 6.3 Antitumor Activity -- 6.4 Cardiovascular Activity -- 6.5 Antithrombotic Activity -- 6.6 Antidiabetic Activity -- 6.7 Gastroprotector Activity -- 6.8 Local Anesthetic Activity -- 6.9 Anxiolytic Activity -- 6.10 Wound-Healing Activity -- 7 Biological Activities of Anethole in Humans -- 8 Conclusions -- References -- 12 The Role of Indirubins in Inflammation and Associated Tumorigenesis -- Abstract -- 1 Introduction -- 2 Chemical Synthesis and Structure-Activity Relationship -- 2.1 Chemical Structure and Synthesis of Indirubin -- 2.2 Structure-Activity Relationship and Chemical Modification -- 3 Noncanonical Indirubins -- 4 Modulation of Signaling Pathways by Indirubins in Inflammation-Associated Cancer -- 5 Nuclear Factor-κB -- 6 Signal Transducer and Activator of Transcription 3 -- 7 Transforming Growth Factor-ß -- 8 Aryl Hydrocarbon Receptor -- 9 Conclusion -- Acknowledgments -- References -- 13 CDDO and Its Role in Chronic Diseases -- Abstract -- 1 Introduction -- 2 Chemical Properties and Pharmacokinetics -- 2.1 Chemical Synthesis and Characteristics -- 2.2 Pharmacokinetics of CDDO -- 3 Signaling Pathways Affected by CDDO -- 3.1 Antioxidant Response and Nrf2 Regulation -- 4 Reactive Oxygen Species and Cell Death: The Primary Target of CDDO -- 4.1 Apoptosis and Necrosis: CDDO Affects Cell Death via Nrf2 -- 5 Other Targets of CDDO: Heat Shock Protein, Telomerase, and MTOR -- 6 Diseases -- 6.1 Cardiac Disease/Vascular Dysfunction -- 6.2 Kidney Disease -- 6.3 AML -- 6.4 Retinal Blindness -- 6.5 Cancer -- 6.6 Liver -- 6.7 Sepsis/Sickle Cell/Lupus -- 7 Conclusion -- References -- 14 Evodiamine and Its Role in Chronic Diseases -- Abstract -- 1 Introduction. , 2 Physicochemical Properties of Evodiamine.
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  • 2
    Keywords: Turmeric -- Therapeutic use. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (500 pages)
    Edition: 1st ed.
    ISBN: 9780387464015
    Series Statement: Advances in Experimental Medicine and Biology Series ; v.595
    DDC: 615/.321
    Language: English
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  • 3
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Toxicology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (479 pages)
    Edition: 1st ed.
    ISBN: 9783319413341
    Series Statement: Advances in Experimental Medicine and Biology Series ; v.928
    DDC: 615.794
    Language: English
    Note: Intro -- Contents -- About the Editors -- 1 Curcumin and Its Role in Chronic Diseases -- Abstract -- 1.1 Introduction -- 1.2 Physical, Chemical and Metabolic Reactions Influencing Curcumin Pharmacology -- 1.2.1 Physicochemical Properties -- 1.2.2 Chemical Structural Features Influencing the Biological Activity of Curcumin -- 1.2.3 Curcumin-Metal Interactions: Role in Curcumin Biology -- 1.2.4 Curcumin Bioavailability -- 1.3 Modulation of Cell Signaling Pathways by Curcumin -- 1.3.1 Growth Factors/Cytokines and Their Receptors -- 1.3.2 Protein Kinases -- 1.3.3 Transcription Factors -- 1.3.4 Gene Expression -- 1.4 Biological Activities of Curcumin in Animal Models -- 1.5 Role of Curcumin in Chronic Diseases -- 1.6 Biological Activities of Curcumin in Humans -- 1.7 Conclusions -- Acknowledgments -- References -- 2 Berberine and Its Role in Chronic Disease -- Abstract -- 2.1 Introduction -- 2.1.1 Physico-Chemical and Pharmacological Properties of Berberine -- 2.1.2 Berberine Modulation of Cell Signalling Pathways -- 2.1.2.1 Berberine Effects on Glucose Metabolism -- 2.1.2.2 Berberine Effects on Lipid Metabolism and Vascular Health -- 2.1.2.3 Berberine and Central Nervous System Disorders -- 2.1.2.4 Tolerability and Safety -- 2.2 Conclusion -- References -- 3 Emodin and Its Role in Chronic Diseases -- Abstract -- 3.1 Introduction -- 3.2 Chemical Structure, Biophysical Properties, and Bioavailability -- 3.3 Role of Emodin in Various Chronic Disorders -- 3.3.1 Allergy -- 3.3.2 Arthritis -- 3.3.3 Cancer -- 3.3.4 Cardiovascular Diseases -- 3.3.5 Diabetes -- 3.3.6 Kidney Diseases -- 3.3.7 Liver Ailments -- 3.3.8 Lung Diseases -- 3.3.9 Neurological Disorders -- 3.3.10 Other Diseases -- 3.3.11 Conclusions and Future Perspective -- References -- 4 Ursolic Acid and Chronic Disease: An Overview of UA's Effects On Prevention and Treatment of Obesity and Cancer. , Abstract -- 4.1 Introduction -- 4.1.1 A Brief Overview of Obesity and Metabolic Syndrome -- 4.1.2 A Brief Overview of Cancer -- 4.2 Mechanistic Links Between Obesity, Metabolic Syndrome Diseases, and Cancer -- 4.3 An Overview of Ursolic Acid -- 4.4 Ursolic Acid and Its Effects on Obesity and Metabolic Syndrome -- 4.5 Ursolic Acid and Its Effects on Cancer -- 4.5.1 Ursolic Acid and Cancer: Notable in vitro Studies -- 4.5.2 Ursolic Acid and Cancer: Notable in vivo Studies -- 4.6 Conclusion -- References -- 5 Tocotrienol and Its Role in Chronic Diseases -- Abstract -- 5.1 Tocotrienol -- 5.2 Antioxidant Effects of Tocotrienol -- 5.3 Anti-inflammatory Effects of Tocotrienol -- 5.4 Tocotrienol as a Hypocholesterolemic Agent -- 5.5 Tocotrienol as Antidiabetic Agent -- 5.6 Tocotrienol as Antiosteporotic Agent -- 5.7 Anticancer Activity -- 5.7.1 Tocotrienol-Induced Caspase Activation and Mode of Cell Death -- 5.7.2 Tocotrienol-Induced Upstream Apoptotic Pathway Modulation -- 5.7.3 Tocotrienol-Induced Anti-angiogenesis and Anti-invasion -- 5.8 Safety of Tocotrienol -- 5.9 Conclusion -- Acknowledgements -- References -- 6 Indole-3-Carbinol and Its Role in Chronic Diseases -- Abstract -- 6.1 Introduction -- 6.2 Physicochemical Properties and Pharmacokinetics of Indole-3-Carbinol -- 6.3 Modulation of Cell Signaling Pathways by Indole-3-Carbinol -- 6.4 Role of Indole-3-Carbinol in Chronic Diseases -- 6.4.1 The Role of I3C in Cancer Controlling -- 6.4.2 Cardiovascular Diseases -- 6.4.3 Obesity and Diabetes -- 6.5 Biological Activities of Indole-3-Carbinol in Animal Models -- 6.6 Biological Activities of Indole-3-Carbinol in Humans -- 6.7 Summary and Conclusions -- References -- 7 Sanguinarine and Its Role in Chronic Diseases -- Abstract -- 7.1 Introduction -- 7.2 Physicochemical Properties of Sanguinarine -- 7.3 Modulation of Cell Signaling Pathways by Sanguinarine. , 7.4 Role of Sanguinarine in Chronic Diseases -- 7.5 Biological Activities of Sanguinarine in Animal Models -- 7.6 Biological Activities of Sanguinarine in Humans -- 7.7 Adverse Effects of Sanguinarine -- 7.8 Conclusions -- Acknowledgments -- References -- 8 Piperine and Its Role in Chronic Diseases -- Abstract -- 8.1 Introduction -- 8.1.1 Pharmacological Properties of Piperine -- 8.2 Role of Piperine in Chronic Diseases -- 8.2.1 Piperine and Oxidative Stress -- 8.2.2 Piperine and Inflammation -- 8.2.3 Piperine Effects on Hepatic Steatosis and Insulin-Resistance -- 8.2.4 Piperine and Anti-depressant Effects -- 8.2.5 Piperine Analgesic and Anti-pyretic Effects -- 8.2.6 Piperine as a Bioavailability Enhancer -- 8.3 Conclusions -- References -- 9 Therapeutic Potential and Molecular Targets of Piceatannol in Chronic Diseases -- Abstract -- 9.1 Introduction -- 9.2 Chemopreventive/Anticarcinogenic Effects -- 9.2.1 Cell Cycle Arrest -- 9.2.2 Induction of Apoptosis -- 9.2.2.1 Hematologic Tumor Cells -- Multiple Myeloma (MM) and Lymphoma -- Leukemia -- 9.2.2.2 Solid Tumor Cells -- 9.2.3 Induction of Autophage -- 9.2.4 DNA Strand Break -- 9.2.5 Anti-metastatic Effects -- 9.2.6 Multidrug Resistance (MDR) Modulation -- 9.2.7 Modulation of Tumor Microenvironment -- 9.2.8 Potentiation of Cytotoxic Effects of Chemotherapeutic Agents -- 9.2.9 Miscellaneous Effects -- 9.3 Other Pharmacological Effects -- 9.3.1 Anti-obesity Effects -- 9.3.2 Antidiabetic Effects -- 9.3.3 Neuroprotective Effects -- 9.3.3.1 Alzheimer Disease (AD) -- 9.3.3.2 Glutamate-Induced Neurotoxicity -- 9.3.3.3 Ischemic Stroke -- 9.3.3.4 Neuroinflammation -- 9.3.4 Cardioprotective Effects -- 9.3.5 Vascular Endothelial Function/Protection -- 9.3.6 Antiallergic Effects -- 9.3.7 Effects on Immune Cell Functions -- 9.3.8 Modulation of Bone Metabolism -- 9.3.9 Anti-aging Effects. , 9.3.9.1 Expansion of Life Span -- 9.3.9.2 Melanogenesis -- 9.3.9.3 Photoaging and Skin Inflammation -- 9.3.10 Anti-colitic Effects -- 9.3.11 Miscellaneous Effects -- 9.3.11.1 Septic Shock -- 9.3.11.2 Retinal/Ocular Protection -- 9.4 Metabolic Formation of PIC -- 9.5 Absorption and Biotransformation -- 9.6 Conclusions and Future Perspectives -- References -- 10 Fisetin and Its Role in Chronic Diseases -- Abstract -- 10.1 Introduction -- 10.2 Physciochemical Properties of Fisetin -- 10.3 Modulation of Cell Signaling Pathways by Fisetin -- 10.4 Role of Fisetin in Chronic Diseases -- 10.4.1 Fisetin and Neurological Diseases -- 10.4.2 Fisetin and Diabetes -- 10.4.3 Fisetin and Obesity -- 10.4.4 Fisetin and Atherosclerosis -- 10.4.5 Fisetin and Skin Cancer -- 10.4.6 Fisetin and Prostate Cancer -- 10.4.7 Fisetin and Colon Cancer -- 10.4.8 Fisetin and Lung Cancer -- 10.4.9 Fisetin and Other Inflammatory Diseases -- 10.5 Conclusions -- Acknowledgments -- References -- 11 Honokiol, an Active Compound of Magnolia Plant, Inhibits Growth, and Progression of Cancers of Different Organs -- Abstract -- 11.1 Introduction -- 11.2 Effect of UVR Exposure on the Skin: Inflammation and Immune Suppression -- 11.3 Treatment of Honokiol Inhibits UVB-Induced Inflammatory Mediators in the Skin -- 11.4 Honokiol Inhibits UVB-Enhanced Expression of Proliferating Cell Nuclear Antigen (PCNA) in the Skin -- 11.5 Honokiol Treatment Inhibits UV Radiation-Induced Skin Tumor Development and Malignant Progression of Papillomas to Carcinomas in Mice -- 11.5.1 Honokiol Controls Cell Cycle Regulators in UVB-Induced Skin Tumors -- 11.5.2 Honokiol Inhibits Cell Survival Signals/Pathways in UVB-Induced Skin Tumors -- 11.6 Honokiol Inhibits Metastatic Potential of Melanoma Cells -- 11.7 Honokiol Promotes Cell Death of Neuroblastoma Cells. , 11.8 Honokiol Inhibits the Growth of Head and Neck Squamous Cell Carcinoma -- 11.9 Protective Effect of Honokiol in Breast Cancer -- 11.10 Growth Inhibitory Effect of Honokiol in Urinary Bladder Cancer -- 11.11 Anti-Tumorigenic Activity of Honokiol in Prostate Cancer -- 11.12 Honokiol Inhibits Metastatic Potential and Tumor Growth of Gastric Cancer -- 11.13 Honokiol Inhibits Migratory Potential of Lung Cancer Cells -- 11.14 Honokiol Inhibits Pancreatic Cancer Growth -- 11.15 Conclusion and Future Prospects -- Acknowledgments -- References -- 12 Celastrol and Its Role in Controlling Chronic Diseases -- Abstract -- 12.1 Introduction -- 12.2 Physico-Chemical Properties of Celastrol -- 12.3 Celastrol Controls Inflammation and Other Pathological Processes in Animal Models of Chronic Diseases -- 12.3.1 Inflammatory, Autoimmune, and Allergic Diseases -- 12.3.2 Neurodegenerative Disorders -- 12.3.3 Other Diseases -- 12.4 Celastrol Modulates Cell Signaling Pathways -- 12.5 Celastrol has Anti-Angiogenic Activity and Protects Against Endothelial Barrier Dysfunction -- 12.6 Celastrol-Induced Modulation of Heat-Shock Response and Its Potential Therapeutic Applications in Chronic Diseases -- 12.7 Anticancer Effects of Celastrol -- 12.8 Use of Celastrol-Containing Natural Products for The Treatment of Chronic Inflammatory and Autoimmune Diseases in Humans -- 12.9 Conclusions -- Acknowledgments -- References -- 13 Boswellic Acids and Their Role in Chronic Inflammatory Diseases -- Abstract -- 13.1 Introductory Remarks -- 13.2 Medical History -- 13.3 Composition of the Resin -- 13.4 Preclinical Studies -- 13.4.1 Anti-inflammatory Actions -- 13.4.1.1 The Arachidonic Acid Cascade: Cyclooxygenase and Cyclooxygenase Products -- 13.4.1.2 The Arachidonic Acid Cascade: 5-Lipoxigenase and 5-Lipoxigenase Products -- 13.4.2 Proteolytic Enzymes: Human Leucocyte Elastase (HLE). , 13.4.3 Oxygen Radicals.
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 318 (1985), S. 665-667 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 SDS-polyacrylamide gel electrophoresis (a) and Mono Q-fast protein liquid chromatography of iodinated TNF-a. (²), The autoradiographs shown in a represent samples from three different iodinations (lanes 1-3). About 10,000 c.p.m. of 125I-TNF were analysed. The Mrs ( x IO3) of protein ...
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  • 5
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Human tumour necrosis factor has about 30% homology in its amino acid sequence with lymphotoxin, a lymphokine that has similar biological properties. Recombinant tumour necrosis factor can be obtained by expression of its complementary DNA in Escherichia coli and induces the haemorrhagic necrosis ...
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  • 6
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A chemically-synthesized gene and natural complementary DNA coding for human lymphotoxin were isolated and engineered for expression in Escherichia coli. Purified recombinant lymphotoxin shows cytotoxic activity on murine and human tumour cell lines in vitro and causes necrosis of certain murine ...
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  • 7
    ISSN: 1432-0851
    Keywords: TNFα ; CD8+ CTL ; IL-2R ; TIL/TAL
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have recently reported that autologous tumor-specific cytotoxic T lymphocyte (CTL) lines and clones can be developed from lymphocytes infiltrating ovarian malignant ascites (TAL). In this study, we investigated the biological effects of tumor necrosis factor α (TNFα) in the induction, expansion, long-term proliferation and lytic function of CD8+ TAL. TNFα up-regulated the IL-2 receptor (IL-2R) α chain (Tac antigen) on the surface of CD3+ CD8+ CD4− TAL, enhanced the proliferation of autologous tumor-specific CTL, and potentiated their lytic function in long-term cultures. Furthermore, in the induction and expansion phase of CD8+ TAL, the presence of TNFα was associated with a selective increase in CD8+ IL-2R+ (Tac+) cells, and subsequent decrease in CD4+ IL-2R+ (Tac+) cells. These results suggest that the observed facilitation of the outgrowth of CD8+ cells in TAL cultures may be due, at least in part, to the up-regulation of IL-2R, and indicate the usefulness of TNFα in the analysis of signalling in autologous tumor-reactive CTL.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Biotherapy 3 (1991), S. 113-120 
    ISSN: 1573-8280
    Keywords: induction ; lymphotoxin ; physicochemical characteristics ; purification ; receptor ; regulation ; source ; structure ; tumor necrosis factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of clinical immunology 19 (1999), S. 350-364 
    ISSN: 1573-2592
    Keywords: Tumor necrosis factor ; signaling ; apoptosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Out of the almost 17 members of the TNF superfamily, TNF is probably the most potent inducer of apoptosis. TNF activates both cell-survival and cell-death mechanisms simultaneously. Activation of NF-kB-dependent genes regulates the survival and proliferative effects pf TNF, whereas activation of caspases regulates the apoptotic effects. TNF-induced apoptosis is mediated primarily through the activation of type I receptors, the death domain of which recruits more than a dozen different signaling proteins, which together are considered part of an apoptotic cascade. This cascade does not, however, account for the role of reactive oxygen intermediates, ceramide, phospholipases, and serine proteases which are also inplicated in TNF-induced apoptosis. This cascade also does not explain how type II TNF receptors which lack the death domain, induce apoptosis. Nevertheless, this review of apoptosis signaling will be limited to those proteins that makeup the cascade.
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  • 10
    ISSN: 1573-2592
    Keywords: Suramin ; tumor cell cytotoxicity ; natural killer cells ; lymphokine-activated killer cells ; monocytes ; tumor necrosis factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Suramin, a polysulfonated naphthylurea, is an antitrypanosomal and antifilarial drug. Because of its anti-reverse transcriptase activity and antiproliferative activity, suramin is also used for the treatment of acquired immunodeficiency syndrome and cancer. In spite of these uses, very little is known about its effects on the immune system. In this report, we investigated the effects of suramin on peripheral blood mononuclear cells. We found that natural killer (NK) cell-mediated cytotoxicity against human erythroblastoid cell line K562 was completely inhibited by suramin in a dose-dependent manner. It also completely blocked lymphokine-activated killer (LAK) cell-mediated cytotoxicity against the human B lymphoblastoid cell lines Raji and Daudi. The cytotoxicity against the human melanoma tumor cell line A-375 mediated by unstimulated and stimulated monocytes was also suppressed by suramin. Maximum inhibition of monocyte-mediated cytotoxicity was observed when suramin was present during both the activation and the effector phases of cytotoxicity. Besides its effects on cell-mediated cytotoxicity, suramin also inhibited the cytotoxic effects of tumor necrosis factor (TNF) against different tumor cell lines. Furthermore, we found that suramin interferes with the binding of TNF with its receptor. Thus our results indicate that suramin overall downregulates the immune system by inhibiting cell-mediated and TNF-mediated cytotoxicity against different tumor cells.
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