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靶向肝癌的天然倍半萜内酯化合物

Acknowledgements第7-9页
摘要第9-12页
Abstract第12-15页
Chapter 1: General Introduction第21-59页
    1.1 Historical perspective of cancer:第21-25页
    1.2 Liver cancer第25-26页
    1.3 Liver cancer modalities第26-33页
        1.3.1 Surgery:第26-27页
        1.3.2 Local ablative therapy:第27页
        1.3.3 Radiofrequency ablation (RFA)第27页
        1.3.4 Microwave ablation (MWA)第27-28页
        1.3.5 Percutaneous ethanol injection (PEI)第28页
        1.3.6 Radiotherapy第28-29页
        1.3.7 Immunotherapy第29-30页
        1.3.8 Transarterial chemoembolization (TACE)第30-31页
        1.3.9 Chemotherapy第31-33页
    1.4 Plant‐derived natural products: an alternative approach for anticancer drugdevelopment第33-35页
    1.5 Phyto‐compounds and HCC第35-45页
        1.5.1 Curcumin第35-36页
        1.5.2 Epigallocatechin gallate第36-37页
        1.5.3 Quercetin第37-38页
        1.5.4 Genistein第38页
        1.5.5 Capsaicin第38-39页
        1.5.6 Silymarin and silibinin第39-40页
        1.5.7 Sesquiterpene Lactones (SLs)第40-45页
            1.5.7.1 Anti-tumor and anti-inflammatory activities of sesquiterpene lactones第41-42页
            1.5.7.2 Anti-cancerous compounds of SLs第42页
            1.5.7.3 Parthenolide (PT)第42-43页
            1.5.7.4 Artemisinin (ART) and its derivatives第43-44页
            1.5.7.5 Costunolide and Dehydrocostuslactone第44-45页
    1.6 Deoxyelephantopin (DET) and Santamarine (STM)第45-49页
        1.6.1 Deoxyelephantopin: Natural sources and biological activities第46-47页
        1.6.2 Santamarine: Natural sources and biological activities第47-49页
    1.7 References第49-59页
Chapter 2: General Material and Methods第59-65页
    2.1 Antibodies and reagents第59页
    2.2 Cell culture第59页
    2.3 Determination of cell viability第59-60页
    2.4 Observation of Morphological Changes第60页
    2.5 Live/Dead Assay第60页
    2.6 Colony forming assay第60-61页
    2.7 Nuclear morphological changes by Hoechst 33258 staining第61页
    2.8 Apoptosis by flow cytometry第61页
    2.9 Measurement of Reactive Oxygen Species (ROS)第61-62页
    2.10 Measurement of mitochondrial membrane potential (ΔΨm)第62页
    2.11 Measurement of Intracellular reduced glutathione (GSH)第62页
    2.12 Thioredoxin reductase (TrxR) assay第62-63页
    2.13 Western blot analysis第63-64页
    2.14 Statistical Analysis第64-65页
Chapter 3: Deoxyelephantopin induces apoptosis in HepG2 cells via oxidative stress, NF-κBinhibition and mitochondrial dysfunction第65-85页
    3.1 Introduction第65-66页
    3.2 Materials and Methods第66-70页
    3.3 Results第70-79页
        3.3.1 DET inhibits proliferation of HepG2 cells第70-72页
        3.3.2 DET induces morphological changes and cell death in HepG2 cells第72-73页
        3.3.3 DET induces apoptosis in HepG2 cells第73页
        3.3.4 DET induces ROS generation in HepG2 cells第73页
        3.3.5 DET disrupts mitochondrial membrane potential (ΔΨm)第73页
        3.3.6 DET depletes intracellular GSH in HepG2 cells第73-75页
        3.3.7 DET inhibits intracellular Thioredoxin reductase (TrxR) activity第75-76页
        3.3.8 DET modulates the expressions of Bcl-2 family proteins第76页
        3.3.9 DET induces Caspase 3 and PARP cleavage第76页
        3.3.10 DET inhibits constitutive and induced NF-кB activation in HepG2 cells第76-79页
    3.4 Discussion第79-81页
    3.5 Conclusion第81-82页
    3.6 References第82-85页
Chapter 4: Santamarine inhibits NF-кB and STAT3 activation and induces apoptosis in HepG2liver cancer Cclls via oxidative stress第85-109页
    4.1 Introduction第85-86页
    4.2 Materials and Methods第86-90页
    4.3 Results第90-102页
        4.3.1 Anti-proliferative effect of STM against HepG2 cells第90-91页
        4.3.2 STM induces morphological changes and cell death in HepG2 cells第91页
        4.3.3 STM induces ROS generation第91页
        4.3.4 STM reduces mitochondrial membrane potential (ΔΨm)第91-93页
        4.3.5 STM diminishes intracellular GSH第93-94页
        4.3.6 STM inhibits intracellular Thioredoxin reductase (TrxR) activity第94-95页
        4.3.7 STM induces mitochondrial mediated (intrinsic) apoptosis第95页
        4.3.8 STM induces extrinsic apoptosis第95-97页
        4.3.9 STM inhibits constitutive and inducible NF-кB activation in HepG2 cells第97-99页
        4.3.10 STM inhibits STAT3 activation in HepG2 cells第99-102页
    4.4 Discussion第102-104页
    4.5 Conclusion第104-105页
    4.6 References第105-109页
Conclusion of the study第109-110页
Papers published during Ph.D第110-111页

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