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    1. Medicin
    2. Klinisk medicin och internmedicin
    3. Sjukdomar och rubbningar
    4. Onkologi

    Perspectives on Biologically Based Cancer Risk Assessment

    AvE. Georg Luebeck,Giovanni A. Zapponi

    Inbunden, Engelska, 1999

    Del i serien Nato Challenges of Modern Society

    1 674 kr

    Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

    Beskrivning

    This text includes a comprehensive updated analysis of cancer risk assessment procedures, with particular attention to biologically-based modelling. The presented arguments include the basic assumptions of cancer risk assessment methods, their biological basis and theoretical background, the relevant data sources, the multistage models (including the two-stage and clonal expansion models and pharmacokinetic models), and the relevant biomarkers, together with fundamental statistical considerations and selected case studies and examples of practical applications. The uncertainty of assessment and the practical use of the proposed methods are suggested. The book examines in detail the updated biologically-based carcinogenic risk assessment procedures together with the usually employed procedures, as well as background information on which they are based. It also proposes new ideas and methods in this field. Furthermore, it includes criteria and methods for practical application and use of the examined procedures.

    Produktinformation

    • Utgivningsdatum:1999-07-31
    • Mått:178 x 254 x 23 mm
    • Vikt:831 g
    • Format:Inbunden
    • Språk:Engelska
    • Serie:Nato Challenges of Modern Society
    • Antal sidor:319
    • Upplaga:1999
    • Förlag:Springer Science+Business Media
    • ISBN:9780306461088

    Utforska kategorier

    • Onkologi inom Medicin
    • Miljövetenskap och miljöpolitik inom Naturvetenskap och teknik

    Innehållsförteckning

    • 1. Introduction.- 1.1. Dose-Response Assessment in Nato Countries.- 1.2. Future Directions in Dose-Response Assessment.- 1.3. Brief Considerations on Some Commonly Used Parameters.- 1.4. Structure of this Report.- 1.5. References.- 2. The Biological Basis of Cancer.- 2.1. Introduction.- 2.2. Cell Proliferation.- 2.3. Cell Proliferation and Mutation.- 2.4. Differences in Susceptibility.- 2.5. Mechanisms of Inhibition in Mutagenesis and Carcinogenesis.- 2.6. References.- 3. Sources of Data For Cancer Risk Assessment.- 3.1. Introduction.- 3.2. In Vitro and Short Term Testing.- 3.3. Trends in Animal Toxicology Testing.- 3.4. Cell Proliferation.- 3.5. Sources of Toxicokinetic Data.- 3.6. Inter- and Intra-Species Variability.- 3.7. References.- 4. Use of Biochemical and Molecular Biomarkers For Cancer Risk Assessment in Humans.- 4.1. Introduction.- 4.2. The Initiatory Complex and its Modulators.- 4.3. The Determinants of the Clonal Expansion of the Initiated Cells.- 4.4. Adjuvant Determinants of the Clonal Expansion.- 4.5. Conclusion.- 4.6. Acknowledgments.- 4.7. References.- 5. The Multistage Model of Carcinogenesis: A Critical Review of its Use.- 5.1. Introduction.- 5.2. Historical Antecedents of the Multistage Model.- 5.3. The Armitage-Doll Multistage Model.- 5.4. Derivation, Rationale and Mathematical Form of the Model.- 5.5. The “Linearized Multistage Model”.- 5.6. Time-Dependent Non-Constant Exposure Patterns: Their Influence on Multistage-Derived Risk Estimates.- 5.7. Consideration of Pharmakokinetics in Multistage Modeling.- 5.8. The Problem of Multiple Exposure: Multistage Carcinogenesis Theory and Additive and Multiplicative Models.- 5.9. Critical Review of the Model.- 5.10. Discussion.- 5.11. References.- 6. Biologically Based Models of Carcinogenesis.- 6.1.Introduction.- 6.2. A Brief History of Biologically-Based Cancer Models.- 6.3. Two-Mutation Clonal Expansion Model.- 6.4. Modes of Action of Carcinogens.- 6.5. Quantitative Formulation of the Model.- 6.6. Likelihood Construction and Estimation.- 6.7. Quantitative Analysis of Intermediate Lesions.- 6.8. Toxicokinetics in Biologically Based Risk Assessment.- 6.9. Interspecies Extrapolation.- 6.10. Implications for Low-Dose Extrapolation.- 6.11. References.- 7. Statistical Issues in the Application of Multistage and Biologically Based Models.- 7.1. Introduction.- 7.2. Characterization Of Models.- 7.3. Statistical Inference.- 7.4. Design Considerations for Low-Dose Problems.- 7.5. Sensitivity Analysis and Physiologically Based Toxicokinetic Modeling.- 7.6. Discussion.- 7.7. References.- 8. Informative Case Studies.- 8.1. Radon, Cigarette Smoke, and Lung Cancer: The Colorado Plateau Uranium Miners’ Cohort.- 8.2. Modeling Colon Cancer.- 8.3. Quantitative Analysis of Enzyme Altered Foci (EAF).- 8.4. The Role of Cell Proliferation in Urinary Bladder Carcinogenesis.- 8.5. N-Nitrosomorpholine: Comparison of Multistage Model and Two-Event Clonal Expansion Model.- 8.6. Calculation of Tetrachloroethylene Risk Estimates.- 8.7. Considerations for Benzene Toxicokinetic Extrapolation.- 8.8. References.- 8.9. Appendix A.- 9. Conclusions and Recommendations.- 9.1. Introduction.- 9.2. What does Each Source of Experimental Data Contribute to our Knowledge and Ability to Model?.- 9.3. What Kinds of Information are Needed to Develop a Biologically Based Model?.- 9.4. How does Linearity Enter into Empirical Models and Biologically Based Models?.- 9.5. How does a Biologically Based Model Help Us Understand Intraspecies Variability?.- 9.6. How Ddoes a Biologically Based Model Help UsUnderstand Interspecies Variability?.- 9.7. What are the Uncertainties Associated with a Biologically Based Model?.- Contributors.