摘要
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.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 1969-1976 |
| 頁數 | 8 |
| 期刊 | Anticancer Research |
| 卷 | 28 |
| 發行號 | 4 A |
| 出版狀態 | 已發佈 - 7月 2008 |
| 對外發佈 | 是 |
UN SDG
此研究成果有助於以下永續發展目標
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SDG 3 良好的健康和福祉
ASJC Scopus subject areas
- 腫瘤科
- 癌症研究
指紋
深入研究「Prostate specific antigen gene expression in androgen insensitive prostate carcinoma subculture cell line」主題。共同形成了獨特的指紋。引用此
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