Abstract
A novel prostate cancer cell line (PC-J) was isolated from an androgen independent non-prostate specific antigen (non-PSA) producing carcinoma cell line. The homologous correlation between PC-J and PC-3 was determined by short tandem repeat analysis. The PSA promoter activity was detected by transient expression assay in the PC-J and LNCaP cells but not in androgen insensitive PC-3 cells. When the PC-J cells were cotransfected with androgen receptor, androgen receptor coactivators and PSA reporter vector cells, the reporter assays indicated that nuclear receptor coactivator 4 (NCOA4) but not androgen receptor activator 24 (ARA24) increased the sensitivity and maximum stimulation of dihydrotestosterone (DHT)-inducing PSA promoter activity. The RT-PCR assays revealed that the expression of several tumor markers, including interleukin-6, prostate stem cell antigen (PSCA), prostate epithelium-specific Ets transcription factor (PDEF) and matriptase, was lower in the PC-J cells than in the PC-3 cells. This cell model elucidated the regulation of PSA expression and enabled comparison of the gene profile at different stages of metastasis in prostatic carcinoma.
| Original language | English |
|---|---|
| Pages (from-to) | 1969-1976 |
| Number of pages | 8 |
| Journal | Anticancer Research |
| Volume | 28 |
| Issue number | 4 A |
| Publication status | Published - Jul 2008 |
| Externally published | Yes |
Keywords
- ARA24
- IL-6
- Matriptase
- NCOA4
- PEDF
- Prostate
- PSA
- PSCA
ASJC Scopus subject areas
- Oncology
- Cancer Research
