Selective inhibition of HTLV-1-infected cell proliferation by a novel tetramethylnaphthalene derivative

Anticancer Res. 2011 Jun;31(6):2241-7.

Abstract

Adult T-cell leukemia (ATL) is caused by infection with human T-lymphotropic virus type 1 (HTLV-1). A novel tetramethylnaphthalene derivative, TMNAA, selectively inhibited the proliferation of various HTLV-1-infected cells, including ATL cell lines and peripheral blood mononuclear cells (PBMCs) from ATL patients. In contrast, the proliferation of uninfected cell lines and PBMCs from healthy donors was hardly affected by the compound. Cell-cycle analysis revealed that TMNAA increased the population of the G0/G1 phase and reduced that of the S phase in HTLV-1-infected cells. TMNAA was found to suppress the phosphorylation of retinoblastoma protein and the expression of cyclin-dependent kinase 4 in HTLV-1-infected cells. Furthermore, the inhibition of cell proliferation was partially annihilated by removing the compound. These results indicate that TMNAA exerts selective inhibition of HTLV-1-infected cells through a novel mechanism, presumably modulating cell cycle regulatory proteins associated with the G0/G1 phase.

MeSH terms

  • Amino Acid Chloromethyl Ketones / pharmacology
  • Caspase Inhibitors
  • Caspases / metabolism
  • Cell Cycle / drug effects
  • Cell Growth Processes / drug effects
  • Cyclin-Dependent Kinase 4 / biosynthesis
  • Enzyme Activation
  • Human T-lymphotropic virus 1 / physiology*
  • Humans
  • Leukemia-Lymphoma, Adult T-Cell / drug therapy*
  • Leukemia-Lymphoma, Adult T-Cell / pathology
  • Leukemia-Lymphoma, Adult T-Cell / virology
  • Naphthalenes / pharmacology*
  • Phosphorylation / drug effects
  • Retinoblastoma Protein / metabolism

Substances

  • Amino Acid Chloromethyl Ketones
  • Caspase Inhibitors
  • Naphthalenes
  • Retinoblastoma Protein
  • benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone
  • CDK4 protein, human
  • Cyclin-Dependent Kinase 4
  • Caspases