Down-regulation of CD44 expression in human prostatic carcinoma cell lines is correlated with DNA hypermethylation

Int J Cancer. 1999 Jan 29;80(3):439-43. doi: 10.1002/(sici)1097-0215(19990129)80:3<439::aid-ijc17>3.0.co;2-v.

Abstract

Down-regulation of the cell-surface adhesion molecule CD44 has been suggested to play an important role in tumor progression and metastasis of prostate cancer. CD44 is encoded by a gene that contains a CpG-rich region (CpG island) in its 5' regulatory sequence. We tried to assess whether hypermethylation of this region is the mechanism responsible for CD44 transcriptional inactivation. A panel of prostatic-carcinoma cell lines, Du145, LNCaP, PC3, PC346C and TSU, was analyzed for CD44 mRNA and protein expression. Du145, PC3 and TSU were positive for CD44, whereas in LNCaP and PC346C both CD44 mRNA and protein expression was suppressed. Methylation-sensitive restriction-enzyme analysis of genomic DNA showed that, in contrast to the CD44-positive cell lines, the CD44-negative lines were hypermethylated in the CD44 promoter CpG island. Furthermore, treatment of a PC346C culture with the demethylating agent 5-azacytidine resulted in re-expression of CD44 mRNA. It is concluded that hypermethylation of the CD44 5' promoter region is one of the mechanisms by which CD44 expression is down-regulated in prostatic-carcinoma cell lines.

MeSH terms

  • Antimetabolites, Antineoplastic / pharmacology
  • Azacitidine / pharmacology
  • CpG Islands / physiology*
  • DNA Methylation*
  • DNA, Neoplasm / metabolism*
  • Down-Regulation
  • Humans
  • Hyaluronan Receptors / genetics
  • Hyaluronan Receptors / metabolism*
  • Male
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / metabolism*
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured

Substances

  • Antimetabolites, Antineoplastic
  • DNA, Neoplasm
  • Hyaluronan Receptors
  • Neoplasm Proteins
  • RNA, Messenger
  • Azacitidine