Immunohistochemical Study of Anti-angiogenesis Property of M
发布时间:2022-12-11 10:56
Background: After the establishment of relationship between angiogenesis and tumorgrowth by Folkman in1971, efforts are being made for treating cancer by targetingangiogenesis. Melanoma differentiation-associated-7(MDA-7) gene is a novel melanomadifferentiation associated gene that functions as a multi-modality anti-cancer agent.Manystudies have demonstrated it antiangiogenesis effect in different tumor models by variousroutes. Objective: The aim of this study to demonstrate its antiangiogene...
【文章页数】:37 页
【学位级别】:硕士
【文章目录】:
Abstract
Chapter 1 Introduction
Chapter 2 Literature Search
2.1 Lymphoma And Angiogenesis
2.2 MDA-7
2.3 MICRO-VESSELS DENSITY
2.4 CD31
Chapter 3 STUDY DESIGN
3.1 PRINCIPLE
3.2 MATERIALS AND METHODS
3.3 Cell Culture
3.4 Animal Experiments
3.5 IVIS System
3.6 Immunohistochemical examination
3.7 Statistical analysis:
Chapter 4 RESULTS
4.1 IL-24 protein secreted capacity of AAV8-MDA7/IL-24 vectors in vivo
4.2 Establishment of lymphoma cells transplanted mouse model
4.3 Suppression of tumor growth in lymphoma model mice after administrated AAV8-MDA7/IL-24
4.4 Suppression of tumor microvessel density in AAV8-MDA7/IL- 24 administrated mice
Chapter 5 Discussion
Chapter 6 Significance of the study
Chapter 7 References
Chapter 8 Declarations
Chapter 9 Introduction To Author
ACKNOWLEDGEMENTS
本文编号:3718656
【文章页数】:37 页
【学位级别】:硕士
【文章目录】:
Abstract
Chapter 1 Introduction
Chapter 2 Literature Search
2.1 Lymphoma And Angiogenesis
2.2 MDA-7
2.3 MICRO-VESSELS DENSITY
2.4 CD31
Chapter 3 STUDY DESIGN
3.1 PRINCIPLE
3.2 MATERIALS AND METHODS
3.3 Cell Culture
3.4 Animal Experiments
3.5 IVIS System
3.6 Immunohistochemical examination
3.7 Statistical analysis:
Chapter 4 RESULTS
4.1 IL-24 protein secreted capacity of AAV8-MDA7/IL-24 vectors in vivo
4.2 Establishment of lymphoma cells transplanted mouse model
4.3 Suppression of tumor growth in lymphoma model mice after administrated AAV8-MDA7/IL-24
4.4 Suppression of tumor microvessel density in AAV8-MDA7/IL- 24 administrated mice
Chapter 5 Discussion
Chapter 6 Significance of the study
Chapter 7 References
Chapter 8 Declarations
Chapter 9 Introduction To Author
ACKNOWLEDGEMENTS
本文编号:3718656
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