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SPOCK1通过NF-κB通路介导EMT促进胰腺癌转移的机制研究

摘要第6-10页
ABSTRACT第10-14页
ABBREVIATIONS第17-18页
1. INTRODUCTION第18-31页
2. MATERIALS AND METHODS第31-46页
    2.1 Materials第31-34页
        2.1.1 Experimental reagents and instruments第31-32页
        2.1.2 Antibodies第32-33页
        2.1.3 Cell culture第33-34页
    2.2 Methods第34-46页
        2.2.1 Plasmid construction and transfection第34-35页
        2.2.2 Cell proliferation assay第35-36页
        2.2.3 Colony formation assay第36页
        2.2.4 5-ethynyl-2'-deoxyuridine (EdU) incorporation assay第36-37页
        2.2.5 Flow cytometry assay第37页
        2.2.6 Immunofluorescence第37-38页
        2.2.7 Wound healing assay第38页
        2.2.8 Tumor cell migration and invasion assay第38-39页
        2.2.9 ZEB2 knockdown using siRNA第39-40页
        2.2.10 Western blot analyses第40-41页
        2.2.11 Dual-luciferase reporter assay第41页
        2.2.12 Mouse xenograft model第41-43页
        2.2.13 Immunohistochemistry第43-44页
        2.2.14 Evaluation of the IHC staining第44-45页
        2.2.15 Statistical analysis第45-46页
3. Results第46-84页
    3.1 SPOCK1 expression is increased and associated with metastasis and poor prognosis in PC第46-51页
    3.2 SPOCK1 accelerates cell proliferation in PC cell lines第51-57页
    3.3 SPOCK1 regulates the PC cell cycle through modulation of G_2/M phase transition第57-61页
    3.4 SPOCK1 regulates the migration, invasion and EMT of PC cells第61-69页
    3.5 The oncogenic activity of SPOCK1 is significantly correlated with activated NF-κB pathway第69-76页
    3.6 SPOCK1/NF-κB/ZEB2 axis is important for the EMT activity of PC cells第76-81页
    3.7 SPOCK1 facilitates PC cell growth and metastasis in vivo第81-84页
4. Discussion第84-90页
5. Conclusions第90-91页
REFERENCES第91-105页
致谢第105-106页
攻读博士学位期间发表的论文及获奖情况第106页

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