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  • 1
    Online Resource
    Online Resource
    Singapore :Springer,
    Keywords: Oxidative stress. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (324 pages)
    Edition: 1st ed.
    ISBN: 9789811605222
    DDC: 571.9453
    Language: English
    Note: Intro -- Contents -- 1: Oxidative Stress and Antioxidant Strategies in Human Diseases -- 1.1 What Is Oxidative Stress? -- 1.2 Prooxidant and Antioxidant Systems -- 1.3 Oxidative Stress and Cancer -- 1.4 Antioxidant Strategies in Cancer -- 1.5 Oxidative Stress and Alzheimer Disease -- 1.6 Antioxidant Strategies in Alzheimer Disease -- 1.7 Oxidative Stress and Cardiovascular Disease -- 1.8 Antioxidant Strategies in Cardiovascular Disease -- 1.9 Concluding Remarks -- References -- 2: Oxidative Stress in the Tumor Immune Microenvironment -- 2.1 Background -- 2.1.1 Oxidative Stress in the Tumor Microenvironment -- 2.1.2 The Major Tumor-Associated Immune Cells -- 2.2 OS and Tumor-Associated Immune Cells -- 2.2.1 The Effects of OS on Teffs in TME -- 2.2.1.1 T Cell Function -- 2.2.1.2 T Cell Differentiation -- 2.2.1.3 T Cell Death -- 2.2.1.4 T Cell Proliferation -- 2.2.2 The Effects of OS on NK Cells in TME -- 2.2.3 The Effects of OS on Tregs in TME -- 2.2.4 The Effects of OS on B Cells in TME -- 2.2.5 The Effects of OS on DCs in TME -- 2.2.6 OS and Macrophages in TME -- 2.2.6.1 OS Effect of TAMs -- 2.2.6.2 The Effect of OS on Macrophages -- 2.3 The Significance of OS on TIME -- 2.3.1 OS and Immunosuppression in TME -- 2.3.2 Inspiration for Clinical Treatment -- 2.4 Summary and Perspectives -- References -- 3: Oxidative Stress-Mediated Stem Cell Aging -- 3.1 Characteristics of Stem Cell Aging -- 3.2 Oxidative Stress-Mediated Signaling Pathways in Stem Cell Aging -- 3.2.1 p53 Pathway -- 3.2.2 Nuclear Factor-E2-Related Factor 2 Pathway -- 3.2.3 FoxOs Signal Pathway -- 3.2.4 Sirtuin Pathway -- 3.2.5 Nuclear Factor Kappa B Pathway -- 3.2.6 PI3K/Akt Signal Pathway -- 3.2.7 p38 MAPK Signal Pathway -- 3.2.8 microRNAs -- 3.3 The Antioxidant Strategy of Stem Cell -- 3.4 Anti-oxidative Stress Strategy in Stem Cell Transplantation Therapy -- 3.5 Conclusion. , References -- 4: Stress Proteins: Biological Functions, Human Diseases, and Virus Infections -- 4.1 Stress Proteins (SPs) -- 4.2 Heat-Shock Proteins (HSPs) -- 4.3 Transcriptional Regulation of the HSPs -- 4.4 Protein Disulfide Isomerase (PDI) -- 4.5 RNA Chaperones -- 4.6 Stress Proteins and Human Diseases -- 4.7 Stress Proteins and Virus Infections -- 4.7.1 Hsp90s in Virus Infection -- 4.7.2 Hsp70s in Virus Infection -- 4.7.3 The Function of Small Heat-Shock Proteins (sHSPs) in Virus Infection -- 4.7.4 The Function of PDIs in Virus Infection -- 4.7.5 The RNA Chaperones in Virus Infection -- 4.8 Antiviral Drug Development and Challenge -- References -- 5: Importance of Mitochondrial Quality Control in Parkinson´s Disease: The Potential Interplay of Mitochondrial Unfolded Prote... -- 5.1 Introduction -- 5.1.1 Reactive Oxygen Species -- 5.2 The Functional Importance of Mitochondria in the Neurons -- 5.3 Mitochondrial Dysfunction in Parkinson´s Disease -- 5.4 The Mitochondrial Unfolded Protein Response (UPRmt) -- 5.4.1 The UPRmt During Mitochondrial Dysfunction -- 5.4.1.1 The Relationship Between the Mitochondrial Protein Import and UPR -- 5.4.1.2 The Regulation of UPRmt in Mammalian Cells -- 5.5 Mitophagy -- 5.5.1 The Mechanism of Ubiquitin-Dependent Mitophagy -- 5.5.2 The Mechanism of Ubiquitin-Independent Mitophagy -- 5.5.3 Mitochondrial Dynamics and Mitophagy -- 5.6 The Relationship of UPRmt and Mitophagy -- 5.6.1 The Role of UPRmt in Parkinson´s Disease -- 5.6.2 The Role of Mitophagy in Parkinson´s Disease -- 5.7 Conclusion and Future Perspectives -- References -- 6: Autophagy in Cellular Stress Responses -- 6.1 Introduction -- 6.2 Oxidative Stress and Autophagy -- 6.3 Endoplasmic Reticulum Stress and Autophagy -- 6.4 Hypoxia-Induced Autophagy -- 6.5 Osmotic Stress and Autophagy -- 6.6 Infection-Induced Autophagy. , 6.6.1 Bacterial Pathogen Infection -- 6.6.2 Virus Infection -- 6.7 Autophagy Under Heat and Cold Stress -- 6.8 Autophagy Inducers or Inhibitors -- 6.9 Conclusions and Perspectives -- References -- 7: Cysteine Metabolism in Cancer Progression and Therapy Resistance -- 7.1 Introduction -- 7.2 Cysteine Homeostasis -- 7.2.1 Dietary Uptake -- 7.2.2 De Novo Biosynthesis through Transsulfuration Pathway -- 7.2.3 Cysteine Salvaged from GSH Degradation through γ-Glutamyl Cycle -- 7.2.4 Scavenge from Protein Degradation -- 7.3 Utilization of Cysteine -- 7.4 Cysteine Catabolism -- 7.5 Regulation of Cysteine Metabolism in Cancer Proliferation and Survival -- 7.5.1 De Novo Transsulfuration Pathway -- 7.5.2 Cystine Uptake by Cystine/Glutamate Antiporter System xc- -- 7.5.3 Regulation of System xc- -- 7.5.3.1 Regulation of Expression by Transcription -- 7.5.3.2 Posttranslational Modifications Affecting System xc- Activity -- 7.5.3.3 Other Modes of System xc- Regulation -- 7.5.4 Cross Talk Between Cysteine Metabolism and Other Metabolic Pathways -- 7.5.5 Cysteine Salvaged from Glutathione Degradation -- 7.6 Cysteine Metabolism in Tumor Microenvironment -- 7.7 Therapeutic Potential of Targeting Cysteine Metabolism in Cancer -- 7.7.1 Targeting System xc-and GSH Homeostasis -- 7.7.2 Targeting Extracellular Cyst(e)ine -- 7.7.3 Targeting Enzymes of the Transsulfuration Pathway -- 7.7.4 Cysteine Metabolism and Therapy Resistance -- 7.8 Conclusions and Perspectives -- References -- 8: Stress and Circadian Rhythms -- 8.1 Stress -- 8.2 Circadian Rhythms -- 8.3 Interaction Between Stress and Circadian Rhythms -- 8.3.1 Molecular Clock in Stress and Circadian Rhythms -- 8.3.2 HPA Axis in Stress and Circadian Rhythms -- 8.4 Diseases Related to Circadian Rhythm under Stress -- 8.4.1 Cardiovascular Disease in Circadian Rhythms and the Molecular Clock. , 8.4.2 The Relationship Between Circadian Rhythm and Brain Gut Axis Diseases -- 8.4.3 The Relationship Between Circadian Rhythm and Liver Diseases -- 8.5 Conclusion -- References -- 9: Reactive Oxygen Species, Glucose Metabolism, and Lipid Metabolism -- 9.1 ROS Generation and ROS Signaling -- 9.2 ROS and Glucose Metabolism -- 9.2.1 Dysregulated Glucose Metabolism Leads to Increased Production of ROS -- 9.2.2 ROS Regulates Glucose Metabolism -- 9.2.2.1 ROS Regulates Glucose Uptake Through GLUT4 -- 9.2.2.2 ROS Regulates Glycolysis -- 9.2.2.3 ROS Regulates Gluconeogenesis -- 9.2.2.4 ROS Regulates Glycogen Synthesis -- 9.2.2.5 ROS Regulates Glycogenolysis -- 9.2.2.6 ROS Regulates Pentose Phosphate Pathway -- 9.3 ROS and Lipid Metabolism -- 9.3.1 Introduction to Lipid Metabolism and ROS -- 9.3.2 Dysregulated Lipid Metabolism Leads to Increased Production of ROS -- 9.3.3 ROS Regulates Lipid Metabolism -- 9.3.3.1 Fatty Acid Synthesis -- 9.3.3.2 Fatty Acid Oxidation -- 9.3.3.3 Phospholipid -- 9.3.3.4 Cholesterol -- 9.3.3.5 Browning of Beige Fat -- 9.4 Conclusion -- References -- 10: Drug Repurposing: An Avenue Toward Stress Medicine in Cancer Therapy -- 10.1 Introduction -- 10.2 Redox Homeostasis -- 10.2.1 Production of Oxidants -- 10.2.2 Antioxidant System -- 10.2.3 Antioxidant Pathway -- 10.3 Drug Repurposing Based on Modulation of Redox Homeostasis -- 10.3.1 Redirecting Oxidizing Agents for Cancer Treatment -- 10.3.1.1 Rediscovery of Traditional Chinese Medicines (TCM) for Cancer Therapy -- 10.3.1.2 Repositioning of Antiviral Drugs to Cancer Treatment -- 10.3.2 Repurposing Molecules Targeting Antioxidant System -- 10.3.2.1 Re-Tasking of SOD Inhibitors for Cancer Treatment -- 10.3.2.2 Repurposing the Trx/TrxR Inhibitors as Anticancer Drugs -- 10.3.2.3 Repositioning the GSH-Depleting Pro-Oxidant to Cancer Treatment -- xCT -- gamma-GCS -- Alkylation of GSH. , 10.3.2.4 Reprofiling Inhibitors of Prxs and Grxs for Cancer Therapy -- 10.3.3 Repurposing Drugs Targeting Redox Signaling for Cancer Therapy -- 10.3.3.1 Extending Nrf2-Targeting Drugs to Cancer-Related Conditions -- 10.3.3.2 Reusing HO-Targeting Reagents as Anticancer Drugs -- 10.3.4 Synergetic Therapy through Weakening Antioxidant Defense Combined with Elevating ROS Production -- 10.4 Conclusion and Perspective -- References -- 11: Redox Regulation of Metabolic Enzymes in Cancer -- 11.1 Redox Regulation of Metabolic Enzymes in Cancer Cells -- 11.1.1 AMPK -- 11.1.2 GAPDH -- 11.1.3 PKM2 -- 11.1.4 LDHA -- 11.1.5 IDH -- 11.2 Targeting the Metabolic Abnormalities in Cancer Cell -- 11.3 Modulating ROS for Cancer Therapy -- 11.4 Conclusion -- References -- 12: Stress and Inflammation -- 12.1 Stress and Diseases -- 12.2 Inflammation and Diseases -- 12.3 Stress and Inflammation -- 12.3.1 Stress, Inflammation, and Cardiovascular Disease -- 12.3.2 Stress, Inflammation, and Metabolic Diseases -- 12.3.3 Stress, Inflammation, and Neurodegenerative Diseases -- 12.3.4 Stress, Inflammation, and Cancer -- 12.3.5 Stress, Inflammation, and Arthritis -- 12.4 Conclusion -- References -- 13: Oxidative Stress in Cell Signaling and Cell Fate Determination Under Glucose Starvation -- 13.1 Introduction -- 13.2 Glucose Uptake and Metabolism -- 13.2.1 Glycolysis -- 13.2.2 The Pentose Phosphate Pathway -- 13.2.3 The Hexosamine Pathway -- 13.2.4 The Serine Biosynthesis Pathway -- 13.2.5 The TCA Cycle and OXPHOS -- 13.3 Reactive Oxygen Species (ROS) and Oxidative Stress -- 13.3.1 ROS -- 13.3.2 The Antioxidant System -- 13.3.3 Oxidative Stress Under Glucose Starvation -- 13.4 AMPK and JNK in Glucose Starvation-Induced Oxidative Stress -- 13.4.1 The Role of AMPK in Redox Homeostasis and Cell Survival Under Glucose Starvation. , 13.4.2 The Role of JNK in the Determination of Cell Fate.
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  • 2
    Publication Date: 2019-01-29
    Description: Rapid declines in Arctic sea ice have captured attention and pose significant challenges to a variety of stakeholders. There is a rising demand for Arctic sea ice prediction at daily to seasonal time scales, which is partly a sea ice initial condition problem. Thus, a multivariate data assimilation that integrates sea ice observations to generate realistic and skillful model initialization is needed to improve predictive skill of Arctic sea ice. Sea ice data assimilation is a relatively new research area. In this review paper, we focus on two challenges for implementing multivariate data assimilation systems for sea ice forecast. First, to address the challenge of limited spatiotemporal coverage and large uncertainties of observations, we discuss sea ice parameters derived from satellite remote sensing that (1) have been utilized for improved model initialization, including concentration, thickness and drift, and (2) are currently under development with the potential for enhancing the predictability of Arctic sea ice, including melt ponds and sea ice leads. Second, to strive to generate the “best” estimate of sea ice initial conditions by combining model simulations/forecasts and observations, we review capabilities and limitations of different data assimilation techniques that have been developed and used to assimilate observed sea ice parameters in dynamical models.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 3
    Publication Date: 2014-01-10
    Description: Analogous precursors in the presence of sulfide dibenzothiophene (DBT) were employed to prepare high-surface area activated carbons (HAC) by KOH chemical activation, in order to investigate the influence of the DBT content on the pore structure of the resultant HAC. The results indicate that the DBT in the precursor can react with and consume a certain amount of the activation agent KOH, thus reducing the actual KOH/coke ratio, which imposes a clear negative effect on the pore structure development. However, regardless of how high the DBT content is in the precursor, no residual sulfur is found in the obtained HAC. The HAC with developed porosity can also be achieved by just increasing the KOH dosage to compensate for the amount consumed in the DBT reaction during the activation process, which provides a high value-added utilization way for organic sulfur-containing minerals. The use of analogous sulfur-containing precursors to investigate the effects of organic sulfide on the pore structure of high-surface area activated carbon (HAC) is reported. Middle- or high-sulfur mineral substances can be employed to prepare high-quality activated carbon for use in practical applications, without any residual sulfur in the HAC obtained.
    Print ISSN: 0930-7516
    Electronic ISSN: 1521-4125
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Published by Wiley-Blackwell
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  • 4
    Publication Date: 2016-06-22
    Description: Nature Immunology 17, 806 (2016). doi:10.1038/ni.3464 Authors: Xia Li, Qian Zhang, Yuanyuan Ding, Yiqi Liu, Dezhi Zhao, Kai Zhao, Qicong Shen, Xingguang Liu, Xuhui Zhu, Nan Li, Zhongyi Cheng, Guoping Fan, Qingqing Wang & Xuetao Cao
    Print ISSN: 1529-2908
    Electronic ISSN: 1529-2916
    Topics: Biology , Medicine
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  • 5
    Publication Date: 2016-07-20
    Description: Nature Immunology 17, 1005 (2016). doi:10.1038/ni0816-1005d Author: Xia Li, Qian Zhang, Yuanyuan Ding, Yiqi Liu, Dezhi Zhao, Kai Zhao, Qicong Shen, Xingguang Liu, Xuhui Zhu, Nan Li, Zhongyi Cheng, Guoping Fan, Qingqing Wang & Xuetao Cao
    Print ISSN: 1529-2908
    Electronic ISSN: 1529-2916
    Topics: Biology , Medicine
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  • 6
    Publication Date: 2016-07-21
    Description: Aortic aneurysms and/or dissection (AADs) in the aorta are a leading cause of human morbidity and mortality. To date, data on non-syndromic thoracic AADs (TAADs) have been mainly derived from Caucasians, and t...
    Electronic ISSN: 1471-2350
    Topics: Biology , Medicine
    Published by BioMed Central
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  • 7
    Publication Date: 2015-01-23
    Description: Natural materials that maintain significant permeability at microwave frequencies are a challenge due to the Snoek limit, but manipulation of matter-microwave interaction in artificial composites provides a possibility to achieve breakthroughs. Herein, we synthesized Fe 3 O 4 /silica core/shell nanoparticles comprised of multiple Fe 3 O 4 cores in each particle (denoted as multiple-Fe 3 O 4 /silica). In comparison to conventional magnetic natural resonance at megahertz frequencies, the resonance of multiple-Fe 3 O 4 /silica composite appears at 9.3 GHz relying on superparamagnetic coupling, which is the highest value reported currently. Our study opens up a fantastic avenue for optimizing micromagnetism by nanoscale architectures.
    Print ISSN: 0003-6951
    Electronic ISSN: 1077-3118
    Topics: Physics
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  • 8
    Publication Date: 2015-01-23
    Description: Background: The mitogen-activated protein kinase kinase/extracellular-signal-regulated kinase (MEK/ERK) signaling pathway is involved in viral life cycle. However, the effect of MEK/ERK pathway in enterovirus 71(EV71)-infected immature dendritic cells (iDCs) is still unclear. Methods: Human peripheral blood mononuclear cells (PBMCs) were isolated and induced to generate iDCs. Unifected iDCs and EV71-infected iDCs with a multiplicity of infection (MOI = 5) were analyzed by flow cytometry. Differential gene expressions of MEK/ERK signaling pathway molecules in EV71-infected iDCs were performed by PCR arrays. The phosphorylation of MEK/ERK pathway molecules in EV71-infected iDCs preincubated without or with U0126 (20 μM) at indicated times was detected by Western blot. The concentrations of IL-1α, IL-2, IL-6, IL-12, TNF-α, IFN-α1, IFN-β and IFN-γ in culture supernatant were analyzed by the luminex fluorescent technique. Results: When iDCs were infected with EV71 for 24 h, the percentage of CD80, CD83, CD86 and HLA-DR expressed on iDCs significantly increased. PCR arrays showed that gene expressions of molecules in MEK/ERK signaling pathway were remarkably upregulated in EV71-infected iDCs. EV71 infection activated both MEK1/2 and ERK1/2, which phosphorylated their downstream transcription factor c-Fos, c-Jun, c-myc and Elk1. Importantly, the treatment of U0126 significantly inhibited MEK/ERK signaling pathway molecules and severely impaired virus replication., Additionally, EV71 infection promoted the expression of son of sevenless (SOS1) and increased the secretion of IL-1α, IL-2, IL-6, IL-12, TNF-α,IFN-β and IFN-γ. Furthermore,the release of IL-1α, IL-2,IL-6 and TNF-α could be effectively suppressed by inhibitor U0126. Conclusions: Our data suggest that the MEK/ERK signaling pathway plays an important role in EV71-infected iDCs and these molecules may be potential targets for the development of new anti-EV71 drugs.
    Electronic ISSN: 1743-422X
    Topics: Medicine
    Published by BioMed Central
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  • 9
    Publication Date: 2015-01-01
    Description: Background: The mitogen-activated protein kinase kinase/extracellular-signal-regulated kinase (MEK/ERK) signaling pathway is involved in viral life cycle. However, the effect of MEK/ERK pathway in enterovirus 71(EV71)-infected immature dendritic cells (iDCs) is still unclear. Methods: Human peripheral blood mononuclear cells (PBMCs) were isolated and induced to generate iDCs. Unifected iDCs and EV71-infected iDCs with a multiplicity of infection (MOI?=?5) were analyzed by flow cytometry. Differential gene expressions of MEK/ERK signaling pathway molecules in EV71-infected iDCs were performed by PCR arrays. The phosphorylation of MEK/ERK pathway molecules in EV71-infected iDCs preincubated without or with U0126 (20??M) at indicated times was detected by Western blot. The concentrations of IL-1?, IL-2, IL-6, IL-12, TNF-?, IFN-?1, IFN-? and IFN-? in culture supernatant were analyzed by the luminex fluorescent technique. Results: When iDCs were infected with EV71 for 24?h, the percentage of CD80, CD83, CD86 and HLA-DR expressed on iDCs significantly increased. PCR arrays showed that gene expressions of molecules in MEK/ERK signaling pathway were remarkably upregulated in EV71-infected iDCs. EV71 infection activated both MEK1/2 and ERK1/2, which phosphorylated their downstream transcription factor c-Fos, c-Jun, c-myc and Elk1. Importantly, the treatment of U0126 significantly inhibited MEK/ERK signaling pathway molecules and severely impaired virus replication., Additionally, EV71 infection promoted the expression of son of sevenless (SOS1) and increased the secretion of IL-1?, IL-2, IL-6, IL-12, TNF-?,IFN-? and IFN-?. Furthermore,the release of IL-1?, IL-2,IL-6 and TNF-? could be effectively suppressed by inhibitor U0126. Conclusions: Our data suggest that the MEK/ERK signaling pathway plays an important role in EV71-infected iDCs and these molecules may be potential targets for the development of new anti-EV71 drugs.
    Electronic ISSN: 1743-422X
    Topics: Medicine
    Published by BioMed Central
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  • 10
    Publication Date: 2016-02-25
    Description: microRNA-186 inhibits cell proliferation and induces apoptosis in human esophageal squamous cell carcinoma by targeting SKP2 Laboratory Investigation 96, 317 (March 2016). doi:10.1038/labinvest.2015.134 Authors: Wei He, Jianfang Feng, Yan Zhang, Yuanyuan Wang, Wenqiao Zang & Guoqiang Zhao
    Print ISSN: 0023-6837
    Electronic ISSN: 1530-0307
    Topics: Medicine
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