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  • 1
    Online Resource
    Online Resource
    Hauppauge :Nova Science Publishers, Incorporated,
    Keywords: Electroporation. ; Electroporation -- Therapeutic use. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (352 pages)
    Edition: 1st ed.
    ISBN: 9781616683832
    Series Statement: None
    DDC: 571.6/4
    Language: English
    Note: Intro -- ELECTROPORATION IN LABORATORY AND CLINICAL INVESTIGATIONS -- ELECTROPORATION IN LABORATORY AND CLINICAL INVESTIGATIONS -- CONTENTS -- PREFACE -- Chapter 1 MATHEMATICAL-PHYSICAL MODELING AND BIOMEDICAL OPTIMIZATION OF CELL ELECTROPERMEABILIZATION: AN OVERVIEW -- ABSTRACT -- INTRODUCTION -- I. ARE THERE ALTERNATIVE MODELS OF ELECTROPERMEABILIZATION? -- II. PHYSICS OF ELECTROPORATION FROM THE GENERAL AND KINETIC STANDPOINTS -- III. MATHEMATICAL MODELING OF ELECTROPORE NUCLEATION AND EVOLUTION -- IV. A DIRECT VIEW ON ELECTROPORE FORMATION: THE PERSPECTIVE OF MOLECULAR SIMULATIONS -- V. THE IN VIVO SETTING -- CONCLUSION -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 2 TECHNICAL ASPECTS OF THE ELECTROCHEMOTHERAPY -- ELECTROPORATION. SHORT DESCRIPTION OF THE PHENOMENON. TRANSMEMBRANE VOLTAGE INDUCED BY ELECTRIC FIELD ON ISOLATED CELL -- TECHNIQUES FOR INDUCING THE ELECTRIC FIELD -- ELECTROPORATION IN CELL SUSPENSION AND TISSUES -- ELECTROCHEMOTHERAPY. ELECTROGENETRANSFECTION -- OPTIMIZATION OF THE PULSE PARAMETERS -- ELECTRODES -- GENERATORS -- RISK OF FIBRILLATION -- OUR OWN STUDIES AND INSTRUMENT DESIGN -- REFERENCES -- Chapter 3 NON-THERMAL IRREVERSIBLE ELECTROPORATION FOR TISSUE ABLATION -- ABSTRACT -- INTRODUCTION -- IRREVERSIBLE ELECTROPORATION FOR NON-THERMAL TISSUE ABLATION -- HISTORY -- THEORY OF IRREVERSIBLE ELECTROPORATION -- NUMERICAL MODELING FOR TREATMENT PLANNING -- Models: -- Electric Field Distribution -- Joule Heating -- COMMON PHYSICAL PROPERTIES: -- Temperature Distribution: -- Equivalent Thermal Dose -- Thermal Damage Equation: -- SPECIAL CONSIDERATIONS -- Heterogeneous Tissue: -- Dynamic Properties During Electroporation -- Temperature Dependent Properties -- CONCLUSION -- REFERENCES -- Chapter 4 MECHANISMS OF MICROORGANISM INACTIVATION BY PULSED ELECTRIC FIELDS -- ABSTRACT -- INTRODUCTION -- THEORY. , COMPARISON WITH EXPERIMENTS AND DISCUSSION -- ACKNOWLEDGMENT -- REFERENCES -- Chapter 5 ELECTROCHEMICAL PROCESSES OCCURING DURING CELL ELECTROMANIPULATION PROCEDURES -- ABSTRACT -- INTRODUCTION -- THEORETICAL BACKGROUND -- Primary Cathodic Half-Reactions -- Primary Anodic Half-Reactions -- Secondary Chemical Reactions -- CONSEQUENCES OF ELECTROCHEMICAL PROCESSES -- Consequences of Cathodic Processes -- Consequences of Anodic Processes -- Consequences of Secondary Chemical Reactions -- CONCLUSION -- ACKNOWLEDGMENT -- REFERENCES -- Chapter 6 ULTRASTRUCTURAL MODIFICATIONS INDUCED BY "ELECTROPORATION" -- ABSTRACT -- INTRODUCTION -- ELECTROPORATION FOR TRANSDERMAL DRUG DELIVERY -- ELECTROPORATION ON MELANOMA XENOGRAFTS -- CONCLUSION -- ACKNOWLEDGMENT -- REFERENCES -- Chapter 7 ELECTROPORATION IN BACTERIA -- ABSTRACT -- INTRODUCTION -- KEY STEPS PRIOR TO ELECTROPORATION -- Preparation of Electrocompetent Cells -- Growth Stage and Concentration of Cells -- Growth Medium Composition and Growth Temperature -- Size, Form, and Concentration of DNA -- Electroporation Buffers and Timing of Plasmid Addition -- ELECTROPORATION CONDITIONS -- Pulsed Electric Field Application -- Electrical Parameters and The Technology of Electroporation -- Post-Pulse Treatments -- EXAMPLES OF APPLICATIONS -- Escherichia Coli -- Preparation of Electrocompetent Cells -- Electroporation -- Lactococcus lactis -- Preparation of Electrocompetent Cells -- Electroporation -- REFERENCES -- Chapter 8 ELECTROPORATION OF PLANT CELLS -- ABSTRACT -- INTRODUCTION -- ELECTROPORATION OF PROTOPLASTS -- ELECTROPORATION OF INTACT PLANT CELLS AND TISSUES -- ELECTROPORATION CONDITIONS -- ELECTROPORATION OF PLANT ORGANELLES -- Chloroplasts -- Mitochondrion -- CONCLUSION -- ACKNOWLEDGMENTS -- REFERENCES. , Chapter 9 ANTI-TUMORAL EFFECTS OF PULSED LOW ELECTRIC FIELD ENHANCED CHEMOTHERAPY: LESSONS FROM EXPERIMENTAL MALIGNANT TUMORS -- ABSTRACT -- 1. INTRODUCTION -- 1.1. Enhancement of the Uptake of Molecules and Macromolecules by Cells -- 1.2. Enhanced Uptake of Molecules and Macromolecules by Non-Permeabilizing Unipolar Pulsed Low Electric Fields (LEF) -- 1.3. The Difference between Enhanced Uptake of Molecules Induced by Electroporation and by Unipolar Pulsed Train of Low Electric Fields (LEF) -- 1.4. Application of Electric Based Cancer Therapy -- 1.4.1. Electrotherapy by Low Intensity DC Electric-Fields (LIEF) -- 1.4.2. Electrochemotherapy by High Electric Fields (ECT) -- 1.4.3. Electrotherapy by High Frequency Electric Fields -- 1.4.4. Electro-Hyperthermia -- 2. ANTI-TUMORAL EFFECTS OF LOW ELECTRIC FIELD CANCER TREATMENT-ENHANCED CHEMOTHERAPY (LEFCT-EC) -- 2.1. Experimental Design And Methods: -- 2.1.1. Experimental Metastatic Tumors -- 2.1.2. Chemotherapy -- 2.1.3. Low Electric Field Cancer Therapy Protocol -- 2.2. Treatment of Mouse Melanoma Derived Tumors by LEFCT-EC -- 2.3. Treatment of Mouse Mammary Carcinoma Derived Tumors by LEFCT-EC -- 2.4. Effective Treatment of Mouse Metastatic Squamous Cell Carcinoma (SCC) Cancer by Low Electric Fields and Chemotherapy -- 2.5. Effective Treatment of Mouse Metastatic Prostate Cancer by Low Electric Fields and Chemotherapy -- 2.6. Cure of Primary Colon Cancer Derived Tumors and Reduction in the Metastatic Load Following LEFCT-EC -- 2.6.1. The Role of the Electric Pulse Intensity -- 2.6.2.The Combination of the Electric Stimulus with Different Chemotherapeutic Drugs. -- 2.6.3. The Ability of LEFCT-EC to Control Primary as Well as Metastatic Disease -- 3. THE INVOLVEMENT OF IMMUNOLOGICAL COMPONENTS IN THE ARREST OF METASTATIC GROWTH ACHIEVED BY DESTRUCTION OF THE PRIMARY TUMOR BY LEFCT AND LEFCT-EC. , 3.1. The Development of an Anti Tumoral Reaction Following LEFCT-EC of B16 Melanoma -- 3.2. Breast Cancer Cell (DA3) Tumor Destruction By LEFCT And LEFCT-EC Triggered Anti Tumor Reaction -- 3.3. SCC Tumor (SQ2) Destruction by LEFCT and LEFCT-EC and Anti Tumor Reaction -- 3.4. Anti Tumor Immunity Against Prostate Cancer Cell Tumors (TRAMP) Following Destruction of the Tumors by LEFCT-EC -- 3.5. Involvement of the Immune Response in the Cure of Metastatic Murine CT-26 Colon Carcinoma by LEFCT-EC -- 3.6 Induction of Anti-Tumor Immunity by other Ablation Mechanisms, Which Cause in Situ Tumor Ablation -- CONCLUSION -- REFERENCES -- Chapter 10 ELECTROGENETHERAPY: ELECTROGENE TRANSFER USING LOW FIELD STRENGTH -- ABSTRACT -- INTRODUCTION -- A NOVEL SYRINGE ELECTRODE USES AMUCH LOWER ELECTRIC FIELD STRENGTH THAN CONVENTIONAL ELECTRODES -- ELECTROPHORESIS ACROSS THE PLASMA MEMBRANE MAY NOT BE INVOLOVED IN IN VIVO DNA TRANSPORT -- THE FIELD STRENGTH FOR ELECTROGENE TRANSFER CAN BE FURTHER REDUCED USING SINE-WAVE CURRENT PULSES -- CONCLUSION -- REFERENCES -- Chapter 11 ELECTROPORATION - TREATING MICE OR MEN? -- ABSTRACT -- INTRODUCTION -- ANIMAL MODELS IN PRECLINICAL STUDIES -- Anemia -- Arthritis -- Diabetes -- Ocular Disease -- Multiple Sclerosis -- Growth Hormone-Releasing Hormone -- Other Studies -- DELIVERY OF DNA VACCINES WITH ELECTROPORATION -- CLINICAL STUDIES -- CONCLUSION -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 12 ELECTROCHEMOTHERAPY IN VETERINARY MEDICINE, PART I: SOLID TUMORS -- ABSTRACT -- PRELIMINARY STUDIES AND FIRST PROTOCOLS -- ELECTROCHEMOTHERAPY FOR SPECIFIC TUMOR TYPES: PHASE II STUDIES -- REFERENCES -- Chapter 13 ELECTROCHEMOTHERAPY IN VETERINARY MEDICINE, PART II: ROUND CELL TUMORS -- ABSTRACT -- PRELIMINARY STUDIES AND FIRST PROTOCOLS -- ELECTROCHEMOTHERAPY FOR SPECIFIC TUMOR TYPES: PHASE II STUDIES -- CONCLUSIONS -- REFERENCES. , Chapter 14 HISTOPATHOLOGICAL ANALYSIS OF CANINE AND FELINE CANCER TREATED WITH ELECTROCHEMOTHERAPY -- ABSTRACT -- MATERIAL AND METHODS -- RESULTS -- DISCUSSION -- REFERENCES -- Chapter 15 CLINICAL APPLICATION OF ELECTROCHEMOTHERAPY - AN ADJUNCT TO SURGERY -- 1. INTRODUCTION -- 2. SYSTEMS AND ELECTRODES EMPLOYED FOR CLINICAL APPLICATION -- 3. APPROPRIATE DRUGS FOR ELECTROCHEMOTHERAPY -- 3.1. Bleomycin -- 3.1.1. Indications -- 3.1.2. Mechanism of Action -- 3.1.3. Clinical Drug Dosage -- 3.1.4. Route of Administration and Timing -- 3.1.5. Toxicity and Side Effects -- 3.2. Cisplatin -- 3.2.1 .Indications -- 3.2.2. Mechanism of Action -- 3.2.3. Drug Dosage -- 3.2.4. Route of Administration and Timing -- 3.2.5. Toxicity and Side Effects -- 4. TREATMENT PROTOCOL -- 4.1. Eligibility Criteria -- 4.2. Anaesthesia -- 4.3. Patient Follow-Up -- 4.4. Response Criteria -- 5. EARLY CLINICAL EXPERIENCE -- 5.1. Clinical Trials Involving Bleomycin -- 5.2. Clinical Trials Involving Cisplatin -- 6. ESOPE TRIAL (TAKEN FROM [20]) -- 6.1. Background -- 6.2. Patient Population -- 6.3. Tumour Histologies -- 6.4. Overall Response -- 6.5. Influence of Drug Delivery -- 6.6. Influence of Tumour Locale -- 6.7. Influence of Tumour Volume -- 6.8. Influence of Electrode Type -- 7. LIMITATIONS OF ELECTROCHEMOTHERAPY -- 7.1. Side Effects Related to Therapy -- 7.2. Patient Referral Criteria -- 7.3. Limitation of Clinical Utility -- 7.4. Need for Comparison Studies with other Therapeutic Modalities -- 8. DEVELOPMENTAL PERSPECTIVES -- 8.1. Extension of Clinical Utility -- 8.2. Enhancement of Existing Therapeutic Regimens -- 8.3. Gene Delivery Vector -- 8.4. Microneedles -- 8.5. Nanoparticles -- CONCLUSIONS -- REFERENCES -- Chapter 16 ELECTROPORATION IN CHRONIC LYMPHOCYTIC LEUKEMIA -- ABSTRACT -- INTRODUCTION -- Chronic Lymphocytic Leukemia. , Opportunities for Gene Transfer in CLL Research.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Munksgaard International Publishers
    Experimental dermatology 14 (2005), S. 0 
    ISSN: 1600-0625
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract:  Apoptosis protease-activating factor-1 (Apaf-1) is a key regulator of the mitochondrial apoptotic pathway, being the central element of the multimeric apoptosome formed by procaspase 9, cytochrome c, and Apaf-1 itself. In this review, the principal aspects about Apaf-1 gene structure and function, and its role in the apoptotic machinery, are described. Moreover, the most recent findings about the involvement of this molecule in melanoma progression and chemoresistance, as well as the clinico-pathological relevance of these findings in the treatment of this deadly disease, are reported.
    Type of Medium: Electronic Resource
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