Antiangiogenic Drugs as Chemosensitizers in Cancer Therapy

Author:   Lucia Morbidelli, PhD (Professor, Department of Life Sciences, University of Siena, Siena, Italy) ,  Lucia Morbidelli, PhD (Professor, Department of Life Sciences, University of Siena, Siena, Italy)
Publisher:   Elsevier Science & Technology
ISBN:  

9780323901901


Pages:   294
Publication Date:   28 January 2022
Format:   Hardback
Availability:   Manufactured on demand   Availability explained
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Antiangiogenic Drugs as Chemosensitizers in Cancer Therapy


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Author:   Lucia Morbidelli, PhD (Professor, Department of Life Sciences, University of Siena, Siena, Italy) ,  Lucia Morbidelli, PhD (Professor, Department of Life Sciences, University of Siena, Siena, Italy)
Publisher:   Elsevier Science & Technology
Imprint:   Academic Press Inc
Weight:   0.770kg
ISBN:  

9780323901901


ISBN 10:   0323901905
Pages:   294
Publication Date:   28 January 2022
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

1. General Introduction to the book2. Angiogenesis: definition and role, cellular and molecular mechanisms, redundancy of angiogenic modulators, receptors and converging signaling3. Anti-angiogenic drugs (monotherapies): General characteristics; molecular mechanisms; efficacy and side effects4. Anti-angiogenic drugs (combination therapies): molecular mechanisms; efficacy and side effects5. Clinical applications in various cancers; state of the art of the approved protocols, ongoing clinical trials, gaps6. Antiangiogenic drugs as chemosensitizer in colorectal cancer7. Antiangiogenic drugs as chemosensitizer in lung cancer8. Antiangiogenic drugs as chemosensitizer for upper GI cancer9. Antiangiogenic drugs as chemosensitizer in breast cancer10. Antiangiogenic drugs as chemosensitizer in renal and genitourinary cancer11. Antiangiogenic drugs as chemosensitizer in skin cancer12. Antiangiogenic drugs as chemosensitizer in brain tumors13. Antiangiogenic drugs as chemosensitizer in circulating tumors14. Antiangiogenic drugs and radiosensitization: state of the art on protocols and experimental studies15. Resistance to combination treatments: mechanisms of resistance to antiangiogenic drugs and cross-talk with tumor cell mechanisms of resistance16. Combination of antiangiogenic drugs with immunotherapies: efficacious synergism; side effects and limits17. Prognostic and diagnostic biomarkers for therapy choice and to monitor antiangiogenic drug efficacy and toxicities18. Antiangiogenic strategies: one target or multitarget inhibitors; synthetic compounds, gene therapy and natural products19. Synthesis and application of dual inhibitors: rationale for development and state of the art of the studies20. Metronomic therapy: mechanisms, advantages and approved protocols alone or in combination21. Personalized medicine with tumor angiogenesis as diagnostic marker and therapeutic target22. General Conclusions and future perspectives

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Dr. Morbidelli’s experience is within the molecular and biochemical pharmacology of angiogenesis and microcirculation and its biological application in diseases and cancer. Through of a plethora of in vitro and in vivo models, she has contributed to the characterization of the pro- and antiangiogenic activities of designed synthetic molecules and natural products and their potential applications in angiogenesis-dependent diseases of the cardiovascular system, ocular disorders, neurovascular diseases and cancer. She co-organized with Professor Bonavida the Fourth International Workshop on “Nitric Oxide in Cancer” held in Sevilla in March 13-14, 2015. The meeting addressed different topics such as NO, mutagenesis, carcinogenesis, tumor promotion and tumor growth; NO regulation of cell death pathways; NO and proliferation and epithelial-mesenchymal transition; Regulation of immune response by NO; Antitumoral activity of NO-based releasing strategies: pre-clinical studies; Antitumoral activity of NO-based releasing strategies: clinical trials.

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