Cell type-/inducer-specific bidirectional regulation by thalidomide and phenylphthalimides of tumor necrosis factor-alpha production and its enantio-dependence

Biochem Biophys Res Commun. 1996 Sep 13;226(2):439-44. doi: 10.1006/bbrc.1996.1374.

Abstract

Regulation by thalidomide and phenylphthalimide analogs (FPP-33 and PPS-33) of TNF-alpha production is specific to cell type and to inducer, i.e., (i) the compounds enhance TPA-induced TNF-alpha production by human leukemia HL-60 cells, while they inhibit TPA-induced TNF-alpha production by another human leukemia cell line, THP-1, and (ii) the compounds inhibit TNF-alpha production by both HL-60 and THP-1 cells when the cells are stimulated with okadaic acid (OA). The structure-activity relationships of these compounds are similar in the four assay systems (TPA/HL-60, TPA/THP-1, OA/HL-60, and OA/THP-1). However, optically active analogs, (S)- and (R)-alpha-methylthalidomides, show distinct bidirectional regulatory effects on TNF-alpha production, i.e., only the (S)-form shows TNF-alpha production-enhancing activity in the TPA/HL-60 assay system, while the (R)-form shows much more potent TNF-alpha production-inhibiting activity than the (S)-form in the other assay systems.

MeSH terms

  • HL-60 Cells
  • Humans
  • Phthalimides / pharmacology*
  • Stereoisomerism
  • Structure-Activity Relationship
  • Thalidomide / pharmacology*
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Phthalimides
  • Tumor Necrosis Factor-alpha
  • Thalidomide