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抗膀胱癌天然化合物木香烯内酯和高氯酸盐血竭素的确定和作用机制研究

ACKNOWLEDGEMENTS第6-8页
ABSTRACT第8-9页
摘要第10-15页
CHAPTER 1: INTRODUCTION第15-35页
    1.1. Urinary Bladder Cancer第15-17页
    1.2. Apoptosis第17-22页
        1.2.1. Reactive oxygen species第19-22页
    1.3. Medicinal Plants第22-34页
        1.3.1. Chinese Traditional Medicines第22-23页
        1.3.2. Sesquiterpene Lactones第23-27页
            1.3.2.1. Costunolide第24-25页
            1.3.2.2. Isoalantolactone第25-26页
            1.3.2.3. Altholactone第26-27页
        1.3.3. Alkaloids第27-30页
            1.3.3.1. Evodiamine第29-30页
        1.3.4. Triterpenoid Saponins第30-31页
            1.3.4.1. Tubeimoside-1第30-31页
        1.3.5. Dracorhodin Perchlorate第31-34页
    1.4. Aims and Objectives of Present Study第34-35页
CHAPTER 2: MATERIAL AND METHODS第35-40页
    2.1. Chemicals and Reagents第35页
    2.2. Cell Culture第35页
    2.3. Cell Proliferation Assay第35-36页
    2.4. Morphological Observation under Phase Contrast and Fluorescence Microscope第36页
    2.5. Live/Dead Assay第36-37页
    2.6. Flow Cytometric Analysis of Cell Cycle第37页
    2.7. Flow Cytometric Determination of Apoptosis第37-38页
    2.8. Flow Cytometric Determination of Reactive Oxygen Species (ROS) in T24 Cells第38页
    2.9. Flow Cytometric Determination of Mitochondrial Membrane Potential (△ψm)第38页
    2.10. Western Blotting第38-39页
    2.11. Statistical Analysis of Data第39-40页
CHAPTER 3: RESULTS第40-76页
    3.1. Sesquiterpene lactones exerts anti-proliferative activity第40-55页
        3.1.1. Costunolide decreases cell proliferation in T24 cells第40-42页
        3.1.2. Costunolide induced morphological changes and ell death in T24 cells第42-45页
        3.1.3. Costunolide Induced G2/M Cell Cycle Arrest in T24 Cells第45-47页
        3.1.4. Costunolide Induced Apoptotic Cell Death in T24 Cells第47-49页
        3.1.5. Costunolide Increased Generation of ROS in T24 Cells第49-51页
        3.1.6. Costunolide Decreased Mitochondrial Membrane Potential in T24 cells第51-53页
        3.1.7. Costunolide Regulated Apoptosis-Related Proteins in T24 Cells第53-55页
    3.2. Dracorhodin perchlorate inhibited proliferation of bladder cancer T24 cells第55-64页
        3.2.1. Dracorhodin perchlorate induced apoptosis in bladder cancer T24 cells第57-59页
        3.2.2. Dracorhodin perchlorate-induced apoptosis was associated with dissipation ofmitochondrial membrane potential第59-61页
        3.2.3. Dracorhodin perchlorate-induced apoptosis was associated with caspase-3activation第61-63页
        3.2.4. Dracorhodin perchlorate down-regulated the expression of Bcl-2,Bcl-X_L, andsurvivin in T24 cells第63-64页
    3.3. Isoalantolactone decreases cell proliferation in T24 cells第64-66页
    3.4. Altholactone decreases cell proliferation in T24 cells第66-68页
    3.5. Alkaloids exert anti-proliferative activity第68-70页
        3.5.1. Evodiamine decreases cell proliferation in T24 cells第68-70页
    3.6. Triterpenoid saponins exert anti-proliferative activity第70-76页
        3.6.1. Tubeimoside-1 decreases cell proliferation in T24 cells第70-72页
        3.6.2. Summary of anti-proliferation effect of sesquiterpene lactones on human bladdercancer cell line T24第72-74页
        3.6.3. The IC50 values of anti-proliferation affect of all five natural compounds used inthis study on human bladder cancer cell ine T24第74-76页
CHAPTER 4: DISCUSSION第76-81页
Novel findings and significance第81-82页
CONCLUSION第82-83页
CHAPTER 5: REFERENCES第83-105页
List of Publications during Master Degree第105-106页
附件第106页

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