Methylation state of the prostate specific membrane antigen (PSMA) CpG island in prostate cancer cell lines.

Abstract:

BACKGROUND:PSMA expression varies among prostate cell lines. We examined the role of CpG methylation and histone deacetylation in PSMA transcriptional repression in prostate cell lines. MATERIALS AND METHODS:The methylation status of a PSMA CpG island was investigated in LNCaP, DU145 and PC3 prostate cell lines. Cells were treated with a demethylating agent and a histone deacetylase inhibitor to determine if PSMA transcription could be activated in nonexpressing cells. A transfection assay with methylated and unmethylated PSMA promoter/enhancer-driven luciferase expression constructs was performed to examine the effect of methylation on transcription. RESULTS:The PSMA CpG island was only methylated in DU145 cells but transcription could not be activated by demethylation or histone deacetylase inhibition. Methylation repressed PSMA transcription in LNCaP cells. CONCLUSION:Although promoter methylation represses PSMA transcription in LNCaP cells, another method inhibits PSMA expression in DU145 and PC3 cells.

journal_name

Anticancer Res

journal_title

Anticancer research

authors

Noss KR,Singal R,Grimes SR

subject

Has Abstract

pub_date

2002-05-01 00:00:00

pages

1505-11

issue

3

eissn

0250-7005

issn

1791-7530

journal_volume

22

pub_type

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