CD86 expression as a surrogate cellular biomarker for pharmacological inhibition of the histone demethylase lysine-specific demethylase 1

Anal Biochem. 2013 Nov 1;442(1):104-6. doi: 10.1016/j.ab.2013.07.032. Epub 2013 Jul 31.

Abstract

There is a lack of rapid cell-based assays that read out enzymatic inhibition of the histone demethylase LSD1 (lysine-specific demethylase 1). Through transcriptome analysis of human acute myeloid leukemia THP1 cells treated with a tranylcypromine-derivative inhibitor of LSD1 active in the low nanomolar range, we identified the cell surface marker CD86 as a sensitive surrogate biomarker of LSD1 inhibition. Within 24h of enzyme inhibition, there was substantial and dose-dependent up-regulation of CD86 expression, as detected by quantitative polymerase chain reaction, flow cytometry, and enzyme-linked immunosorbent assay. Thus, the use of CD86 expression may facilitate screening of compounds with putative LSD1 inhibitory activities in cellular assays.

Keywords: Acute myeloid leukemia; Assay; Biomarker; CD86; Inhibitors; LSD1.

MeSH terms

  • B7-2 Antigen / antagonists & inhibitors*
  • B7-2 Antigen / biosynthesis*
  • B7-2 Antigen / genetics
  • Biomarkers / metabolism
  • Cell Line, Tumor
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Histone Demethylases / antagonists & inhibitors*
  • Histone Demethylases / metabolism
  • Humans
  • Leukemia, Myeloid, Acute / drug therapy*
  • Leukemia, Myeloid, Acute / metabolism
  • Leukemia, Myeloid, Acute / pathology
  • Structure-Activity Relationship
  • Tranylcypromine / chemistry
  • Tranylcypromine / pharmacology*
  • Up-Regulation / drug effects

Substances

  • B7-2 Antigen
  • Biomarkers
  • CD86 protein, human
  • Enzyme Inhibitors
  • Tranylcypromine
  • Histone Demethylases
  • KDM1A protein, human