Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(NES-TVA)J12Ech mutation
(2 available)
Trp53tm1Brd mutation
(5 available);
any
Trp53 mutation
(232 available)
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nervous system
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• 3 of 8 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 17 of 39 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
• however, mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR do not develop gliomas
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• in mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF
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neoplasm
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• 3 of 8 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 17 of 39 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
• however, mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR do not develop gliomas
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Rdp mutation
(6 available);
any
Cdkn2a mutation
(62 available)
Tg(NES-TVA)J12Ech mutation
(2 available)
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neoplasm
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• 13 of 25 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice
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nervous system
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• 13 of 25 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Rdp mutation
(6 available);
any
Cdkn2a mutation
(62 available)
Tg(NES-TVA)J12Ech mutation
(2 available)
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nervous system
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• 8 of 19 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice
• 4 of 10 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 6 of 16 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
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• in mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and bFGF or Cdk4
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neoplasm
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• 8 of 19 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR develop gliomas unlike similarly treated wild-type mice
• 4 of 10 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR and Cdk4 develop gliomas compared to 1 of 8 similarly treated wild-type mice
• 6 of 16 mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR, Cdk4, and bFGF develop gliomas compared to 3 of 29 similarly treated wild-type mice
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm2.1Rdp mutation
(2 available);
any
Cdkn2a mutation
(62 available)
Tg(NES-TVA)J12Ech mutation
(2 available)
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mortality/aging
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• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 20% compared to 50% survival in similarly treated Tg(NES-TVA)12Hev mice
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neoplasm
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• 22 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
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• 21 grade II (similar to human oligodendroglioma) and 1 grade III (similar to anaplastic oligodendroglioma)
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nervous system
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• 22 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
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• 21 grade II (similar to human oligodendroglioma) and 1 grade III (similar to anaplastic oligodendroglioma)
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Rdp mutation
(6 available);
any
Cdkn2a mutation
(62 available)
Tg(NES-TVA)J12Ech mutation
(2 available)
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mortality/aging
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• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 15% compared to 50% survival in similarly treated Tg(NES-TVA)12Hev mice
(J:125535)
• co delivery of RCAS-PDGFB and an antisense construct targeting Igfbp2 results in improved survival compared to mice infected with RCAS-PDGFB alone
(J:153220)
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neoplasm
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• 17 gliomas are discovered in 20 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 6 grade II (similar to human oligodendroglioma) and 11 grade III (similar to anaplastic oligodendroglioma)
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• infection with RCAS-PDGFB induces anaplastic oligodendrogliomas in 97% of mice
• tumors are highly aggressive and display multiple foci of pseudopalisading necrosis and microvascular proliferation
• co-infection with RCAS-PDGFB and RCAS-IGFBP2 results in tumors that are histopathologically identical to those in mice infected with only RCAS-PDGFB
• co delivery of RCAS-PDGFB and an antisense construct targeting Igfbp2 results in a primarily anaplastic oligodendrogliomas but 18% of tumors are lower grade oligodendrogliomas
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nervous system
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• 17 gliomas are discovered in 20 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
• 6 grade II (similar to human oligodendroglioma) and 11 grade III (similar to anaplastic oligodendroglioma)
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• infection with RCAS-PDGFB induces anaplastic oligodendrogliomas in 97% of mice
• tumors are highly aggressive and display multiple foci of pseudopalisading necrosis and microvascular proliferation
• co-infection with RCAS-PDGFB and RCAS-IGFBP2 results in tumors that are histopathologically identical to those in mice infected with only RCAS-PDGFB
• co delivery of RCAS-PDGFB and an antisense construct targeting Igfbp2 results in a primarily anaplastic oligodendrogliomas but 18% of tumors are lower grade oligodendrogliomas
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn2atm1Cjs mutation
(6 available);
any
Cdkn2a mutation
(62 available)
Tg(NES-TVA)J12Ech mutation
(2 available)
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mortality/aging
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• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 40% compared to 50% survival in similarly treated Tg(NES-TVA)12Hev mice
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neoplasm
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• 22 gliomas are discovered in 35 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
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• 10 grade II (similar to human oligodendroglioma) and 12 grade III (similar to anaplastic oligodendroglioma)
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nervous system
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• 22 gliomas are discovered in 35 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
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• 10 grade II (similar to human oligodendroglioma) and 12 grade III (similar to anaplastic oligodendroglioma)
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Allelic Composition |
Tg(NES-TVA)J12Ech/0
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Genetic Background |
involves: 129 * C57BL/6 * FVB/N |
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(NES-TVA)J12Ech mutation
(2 available)
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neoplasm
N |
• mice transfected with replication-competent ALV splice acceptor viral vector expressing a constitutively active EGFR do not develop gliomas
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(NES-TVA)J12Ech mutation
(2 available)
|
|
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mortality/aging
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• after 84 days, mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB exhibit 50% survival
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neoplasm
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• 14 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
|
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• 11 grade II (similar to human oligodendroglioma) and 3 grade III (similar to anaplastic oligodendroglioma)
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nervous system
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• 14 gliomas are discovered in 28 mice transfected with replication-competent ALV splice acceptor viral vector expressing PDGFB
|
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• 11 grade II (similar to human oligodendroglioma) and 3 grade III (similar to anaplastic oligodendroglioma)
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