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Phenotypes Associated with This Genotype
Genotype
MGI:3831293
Allelic
Composition
Hprt1tm1(Pbsn*-cre/ERT2)Jir/Y
Ptentm2Mak/Ptentm2Mak
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hprt1tm1(Pbsn*-cre/ERT2)Jir mutation (0 available); any Hprt1 mutation (1280 available)
Ptentm2Mak mutation (4 available); any Pten mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• carcinoma develops in the prostate at different rates depending on age of mouse when tamoxifen administration occurs
• when tamoxifen is given to mice at two weeks of age, overt neoplasia and microinvasive carcinoma are evident 10 to 12 weeks later in one-third of mice
• when tamoxifen is given to mice 6 weeks of age, a more gradual progression to carcinoma occurs with overtly malignant lesions not present until 1 year of age
• when tamoxifen is given to mice at 2 weeks of age, hyperplastic regions as well as low grade PIN lesions and an increased number of apoptotic cells are evident 4 to 6 weeks later
• by 10-12 weeks post injection, all mice display increased proliferation of the prostate epithelium and high grade PIN lesions with a third of the mice having microinvasive carcinomas
• when tamoxifen is given to mice at 6 weeks of age, early hyperplastic lesions and increased proliferation rates of the prostate epithelium are evident 4 weeks later
• about half the mice exhibit advanced PIN lesions at 16-20 weeks after tamoxifen administration at 6 weeks of age

endocrine/exocrine glands
• carcinoma develops in the prostate at different rates depending on age of mouse when tamoxifen administration occurs
• when tamoxifen is given to mice at two weeks of age, overt neoplasia and microinvasive carcinoma are evident 10 to 12 weeks later in one-third of mice
• when tamoxifen is given to mice 6 weeks of age, a more gradual progression to carcinoma occurs with overtly malignant lesions not present until 1 year of age
• when tamoxifen is given to mice at 2 weeks of age, hyperplastic regions as well as low grade PIN lesions and an increased number of apoptotic cells are evident 4 to 6 weeks later
• by 10-12 weeks post injection, all mice display increased proliferation of the prostate epithelium and high grade PIN lesions with a third of the mice having microinvasive carcinomas
• when tamoxifen is given to mice at 6 weeks of age, early hyperplastic lesions and increased proliferation rates of the prostate epithelium are evident 4 weeks later
• about half the mice exhibit advanced PIN lesions at 16-20 weeks after tamoxifen administration at 6 weeks of age

reproductive system
• carcinoma develops in the prostate at different rates depending on age of mouse when tamoxifen administration occurs
• when tamoxifen is given to mice at two weeks of age, overt neoplasia and microinvasive carcinoma are evident 10 to 12 weeks later in one-third of mice
• when tamoxifen is given to mice 6 weeks of age, a more gradual progression to carcinoma occurs with overtly malignant lesions not present until 1 year of age
• when tamoxifen is given to mice at 2 weeks of age, hyperplastic regions as well as low grade PIN lesions and an increased number of apoptotic cells are evident 4 to 6 weeks later
• by 10-12 weeks post injection, all mice display increased proliferation of the prostate epithelium and high grade PIN lesions with a third of the mice having microinvasive carcinomas
• when tamoxifen is given to mice at 6 weeks of age, early hyperplastic lesions and increased proliferation rates of the prostate epithelium are evident 4 weeks later
• about half the mice exhibit advanced PIN lesions at 16-20 weeks after tamoxifen administration at 6 weeks of age


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory