Table 5.
Model | Alteration | Driver and/or Add. Genetic Alteration |
Phenotype | Reference |
---|---|---|---|---|
Nkx3.1 | Loss of expression | Hemizygous loss of Pten (germline heterozygous Pten allele) |
HGPIN with invasive adenocarcinoma |
[55,56] |
p27Kip1 | Loss of expression | Hemizygous loss of Pten
(germline heterozygous Pten allele) |
HGPIN with invasive adenocarcinoma |
[57,58] |
Aft3 | Loss of expression | Homozygous loss of Pten
(conditional Pten allele) |
HGPIN with invasive adenocarcinoma |
[59] |
Apcflox | Loss of expression | PBCre4 driver | HGPIN followed by local adenocarcinoma |
[60] |
Bmi1 | Gain of expression | Hemizygous loss of Pten
(germline heterozygous Pten allele) |
Locally invasive and highly vascularized adenocarcinoma, with frequent bladder outlet obstruction | [61] |
Tsc2 | Loss of expression | Hemizygous loss of Pten (germline heterozygous Pten allele) |
Invasive adenocarcinoma; enhanced lymphoid proliferation; development of skin cancer |
[62] |
Phlpp1 | Loss of expression | Hemizygous loss of Pten
(germline heterozygous Pten allele) |
Invasive adenocarcinoma at full penetrance with onset of 8 months |
[63] |
Chk1 | Loss of expression | Hemizygous loss of Pten (germline heterozygous Pten allele) |
Progression of HGPIN into invasive adenocarcinoma |
[64] |
PK C ε | Gain of expression | Hemizygous loss of Pten
(germline heterozygous Pten allele) |
Invasive adenocarcinoma, preferentially in ventral prostate |
[65] |
Gata3 | Loss of expression | Homozygous loss of Pten
(conditional Pten allele) |
Acceleration of invasive adenocarcinoma |
[66] |
Erg | Gain of expression | Homozygous loss of Pten
(conditional Pten allele) |
Foci of invasive adenocarcinoma with varying levels of Erg expression | [67,68] |
Etv1 | Gain of expression | Homozygous loss of Pten
(conditional Pten allele) |
Invasive adenocarcinoma with homogenous Etv1 expression | [69] |
Junb | Loss of expression | Homozygous loss of Pten
(conditional Pten allele) |
Invasive adenocarcinoma in anterior prostate, with strong histological similarity to human PCa | [70] |
SPOP- F133V |
Gain of expression | Homozygous loss of Pten
(conditional Pten allele) |
Invasive, poorly differentiated, and highly proliferative adenocarcinoma | [71] |
PSGR | Gain of expression | Homozygous loss of Pten
(conditional Pten allele) |
Invasive adenocarcinoma featuring Akt activation and extensive inflammatory cell infiltration |
[72] |
Zbtb7a | Loss of expression | Homozygous loss of Pten
(conditional Pten allele) |
Highly penetrant invasive adenocarcinoma at 11 weeks |
[73] |
Hepsin | Gain of expression |
Myc gain of expression under control of PB driver |
Invasive adenocarcinoma lacking glandular prostate differentiation and clear basement membrane contour | [74] |
MMP7 | Gain of expression | Loss of Pten function | Invasive adenocarcinoma through induction of epithelial-to-mesenchymal transition (EMT) | [75] |
Ptenadcre+ (1) | Loss of expression | Cre-expressing adenovirus via intraductal injection into anterior- posterior prostate |
Invasive adenocarcinoma with onset of 8–16 weeks | [76] |
Kindlin-3 | Loss of expression | Xenograft | Subcutaneous prostate cancer tumor growth | [77] |
(1)Ptenadcre+: indicates model with Cre-expressing adenovirus used to disrupt Pten.