neoplasm
• decreased vascular densities, increase in vessel disruptions, and reduced vascular spouting in tumors formed by injection of Lewis lung carcinoma cells
• coverage of tumor vessels with alpha-SMA+ mural cells and basement membrane is decreased and vascular permeability is increased
• vascular densities are also reduced in tumors formed by injected B16F10 melanoma cells
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• in tumors formed by injection of Lewis lung carcinoma cells
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• tumors formed by injection of Lewis lung carcinoma cells show an increase in hemorrhagic foci and increased hypoxia with extensive apoptosis in the center of the tumor
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• decreased growth of injected Lewis lung carcinoma cells
• tumor growth is also delayed for injected B16F10 melanoma cells
• impact of cisplatin, VEGF-A blockade, or combretastatin-A4-phosphate on Lewis lung carcinoma cell tumor growth/necrosis is enhanced compared to wild-type controls
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homeostasis/metabolism
• impact of cisplatin on Lewis lung carcinoma cell tumor growth/necrosis is enhanced compared to wild-type controls
• impact of combretastatin-A4-phosphate treatment on inhibition of tumor growth and inhibition of tumor vascularization is enhanced
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cardiovascular system
N |
• no differences from wild-type controls in vascular morphology or integrity are found in untreated mice
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• decreased vascular densities, increase in vessel disruptions, and reduced vascular spouting in tumors formed by injection of Lewis lung carcinoma cells
• coverage of tumor vessels with alpha-SMA+ mural cells and basement membrane is decreased and vascular permeability is increased
• vascular densities are also reduced in tumors formed by injected B16F10 melanoma cells
|
• tumors formed by injection of Lewis lung carcinoma cells show an increase in hemorrhagic foci
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