Phenotypes associated with this allele
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epn1tm1.1Wami mutation
(0 available);
any
Epn1 mutation
(32 available)
Epn2tm1Ocr mutation
(0 available);
any
Epn2 mutation
(73 available)
Tg(Cdh5-cre/ERT2)CIVE23Mlia mutation
(0 available)
Tg(TRAMP)8247Ng mutation
(1 available)
|
|
|
Reduced tumor growth in Epn1tm1.1Wami/Epn1tm1.1Wami Epn2tm1Ocr/Epn2tm1Ocr Tg(Cdh5-cre/ERT2)CIVE23Mlia/0 Tg(TRAMP)8247Ng/0 mice
mortality/aging
|
• tamoxifen-treated mice exhibit decreased mortality compared with Tg(TRAMP)8247Ng control mice
|
neoplasm
|
• tamoxifen-treated mice develop smaller tumors compared with Tg(TRAMP)8247Ng control mice
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epn1tm1.1Wami mutation
(0 available);
any
Epn1 mutation
(32 available)
Epn2tm1Ocr mutation
(0 available);
any
Epn2 mutation
(73 available)
Tg(Cdh5-cre/ERT2)CIVE23Mlia mutation
(0 available)
|
|
|
Disrupted endothelial junctions in tumor vessels of Epn1tm1.1Wami/Epn1tm1.1Wami Epn2tm1Ocr/Epn2tm1Ocr Tg(Cdh5-cre/ERT2)CIVE23Mlia/0 mice
mortality/aging
|
• tamoxifen-treated mice transplanted with GL261glioma cells survive longer than with control mice
|
neoplasm
|
• tamoxifen-treated mice transplanted with Lewis Lung carcinoma (LLC) cells exhibit disorganized, fragile, immature, enlarged and leaky tumor vessels compared with control mice
• however, treatment with a VEGFR2 kinase inhibitor restored tumor vasculature
|
|
• tamoxifen-treated mice subjected to AOM/DSS exhibit reduced tumor incidence and decreased tumor growth compared with control mice
|
|
• tamoxifen-treated mice transplanted with Lewis Lung carcinoma (LLC) cells develop fewer, smaller tumors that grow at a slower rate compared with control mice
• tamoxifen-treated mice transplanted with GL261glioma cells develop smaller tumors compared with control mice
• tamoxifen-treated mice subjected to AOM/DSS exhibit reduced tumor incidence and decreased tumor growth compared with control mice
|
cardiovascular system
|
• tamoxifen-treated mice transplanted with Lewis Lung carcinoma (LLC) cells exhibit disorganized, fragile, immature, enlarged and leaky tumor vessels compared with control mice
• however, treatment with a VEGFR2 kinase inhibitor restored tumor vasculature
|
|
• endothelial cells treated with tamoxifen exhibit enhanced VEGF-stimulated migration compared with control cells
|
|
• endothelial cells treated with tamoxifen exhibit disrupted endothelial junctions compared with control cells
|
|
• endothelial cells treated with tamoxifen exhibit enhanced VEGF-stimulated proliferation compared with control cells
|
|
• of tumor vasculature in tamoxifen-treated mice transplanted with Lewis Lung carcinoma (LLC) cells
• however, vascular permeability of blood vessels in major organs is normal
|
cellular
|
• endothelial cells treated with tamoxifen exhibit enhanced VEGF-stimulated migration compared with control cells
|
|
• endothelial cells treated with tamoxifen exhibit enhanced VEGF-stimulated proliferation compared with control cells
|
homeostasis/metabolism