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Prostate specific antigen gene expression in androgen insensitive prostate carcinoma subculture cell line

  • Ke Hung Tsui
  • , Tsui Hsia Feng
  • , Li Chuan Chung
  • , Chun Hsiang Chao
  • , Phei Lang Chang
  • , Horng Heng Juang

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)1969-1976
Number of pages8
JournalAnticancer Research
Volume28
Issue number4 A
Publication statusPublished - Jul 2008
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • ARA24
  • IL-6
  • Matriptase
  • NCOA4
  • PEDF
  • Prostate
  • PSA
  • PSCA

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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