The histone deacetylase inhibitor SAHA arrests cancer cell growth, up-regulates thioredoxin-binding protein-2, and down-regulates thioredoxin

Proc Natl Acad Sci U S A. 2002 Sep 3;99(18):11700-5. doi: 10.1073/pnas.182372299. Epub 2002 Aug 20.

Abstract

Suberoylanilide hydroxamic acid (SAHA) is a potent inhibitor of histone deacetylases (HDACs) that causes growth arrest, differentiation, and/or apoptosis of many tumor types in vitro and in vivo. SAHA is in clinical trials for the treatment of cancer. HDAC inhibitors induce the expression of less than 2% of genes in cultured cells. In this study we show that SAHA induces the expression of vitamin D-up-regulated protein 1/thioredoxin-binding protein-2 (TBP-2) in transformed cells. As the expression of TBP-2 mRNA is increased, the expression of a second gene, thioredoxin, is decreased. In transient transfection assays, HDAC inhibitors induce TBP-2 promoter constructs, and this induction requires an NF-Y binding site. We report here that TBP-2 expression is reduced in human primary breast and colon tumors compared with adjacent tissue. These results support a model in which the expression of a subset of genes (i.e., including TBP-2) is repressed in transformed cells, leading to a block in differentiation, and culture of transformed cells with SAHA causes re-expression of these genes, leading to induction of growth arrest, differentiation, and/or apoptosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apoptosis / drug effects
  • Base Sequence
  • Carrier Proteins / genetics*
  • Cell Division / drug effects*
  • Cloning, Molecular
  • DNA Primers
  • Down-Regulation / drug effects
  • Enzyme Inhibitors / pharmacology*
  • Histone Deacetylase Inhibitors*
  • Humans
  • Hydroxamic Acids / pharmacology*
  • Molecular Sequence Data
  • Neoplasms / pathology*
  • RNA, Messenger / genetics
  • Thioredoxins / genetics*
  • Tumor Cells, Cultured
  • Up-Regulation / drug effects
  • Vorinostat

Substances

  • Carrier Proteins
  • DNA Primers
  • Enzyme Inhibitors
  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • RNA, Messenger
  • TXNIP protein, human
  • Thioredoxins
  • Vorinostat

Associated data

  • GENBANK/AF408392