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

被引:46
|
作者
Lynch, James T. [1 ]
Cockerill, Mark J. [2 ]
Hitchin, James R. [2 ]
Wiseman, Daniel H. [1 ]
Somervaille, Tim C. P. [1 ]
机构
[1] Univ Manchester, Paterson Inst Canc Res, Canc Res UK Leukaemia Biol Lab, Manchester M20 4BX, Lancs, England
[2] Univ Manchester, Paterson Inst Canc Res, Canc Res UK Drug Discovery Unit, Manchester M20 4BX, Lancs, England
关键词
LSD1; CD86; Acute myeloid leukemia; Inhibitors; Assay; Biomarker; LSD1; TRANS-2-PHENYLCYCLOPROPYLAMINE; CANCER;
D O I
10.1016/j.ab.2013.07.032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 24 h 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. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:104 / 106
页数:3
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