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Phenotypes Associated with This Genotype
Genotype
MGI:5636613
Allelic
Composition
Ptentm2Mak/Ptentm2Mak
Tg(KLK3-cre)13Saa/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptentm2Mak mutation (4 available); any Pten mutation (88 available)
Tg(KLK3-cre)13Saa mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mean survival time is 90.5 weeks of age

neoplasm
• mice show early formation of prostate tumors before 20 weeks of age
• tumors in 20 week old mice show an initial response to androgen deprivation therapy (by surgical castration), however by 8 weeks post-castration, mice develop castration-resistant prostate cancer in which tumors are insensitive to everolimus, a PI3K/AKT targeted therapy
• castration-resistant prostate tumors however are sensitive to a combination therapy of everolimus and U0126, a MEK1/2 inhibitor, showing increased apoptosis following treatment
• from 20 weeks, all mice develop adenocarcinomas in the lateral, dorsal, and ventral prostate lobes, however tumors in the anterior prostate are rare
• mice gradually develop prostatic intraepithelial neoplasia as early as 8 weeks in the dorsolateral lobes that progress to well-differentiated tumors by 15 weeks
• at 50-60 weeks of age, 10% of mice develop distant spread of tumor metastases primarily in the loco-regional lymph nodes and occasionally in lung and liver
• by 75-90 weeks of age, about 60% of mice show distant spread of tumor metastases

reproductive system
• mice show early formation of prostate tumors before 20 weeks of age
• tumors in 20 week old mice show an initial response to androgen deprivation therapy (by surgical castration), however by 8 weeks post-castration, mice develop castration-resistant prostate cancer in which tumors are insensitive to everolimus, a PI3K/AKT targeted therapy
• castration-resistant prostate tumors however are sensitive to a combination therapy of everolimus and U0126, a MEK1/2 inhibitor, showing increased apoptosis following treatment
• from 20 weeks, all mice develop adenocarcinomas in the lateral, dorsal, and ventral prostate lobes, however tumors in the anterior prostate are rare
• mice gradually develop prostatic intraepithelial neoplasia as early as 8 weeks in the dorsolateral lobes that progress to well-differentiated tumors by 15 weeks

endocrine/exocrine glands
• mice show early formation of prostate tumors before 20 weeks of age
• tumors in 20 week old mice show an initial response to androgen deprivation therapy (by surgical castration), however by 8 weeks post-castration, mice develop castration-resistant prostate cancer in which tumors are insensitive to everolimus, a PI3K/AKT targeted therapy
• castration-resistant prostate tumors however are sensitive to a combination therapy of everolimus and U0126, a MEK1/2 inhibitor, showing increased apoptosis following treatment
• from 20 weeks, all mice develop adenocarcinomas in the lateral, dorsal, and ventral prostate lobes, however tumors in the anterior prostate are rare
• mice gradually develop prostatic intraepithelial neoplasia as early as 8 weeks in the dorsolateral lobes that progress to well-differentiated tumors by 15 weeks


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
12/10/2024
MGI 6.24
The Jackson Laboratory