Evaluating biological activity of compounds by transcription factor activity profiling

被引:20
|
作者
Medvedev, Alexander [1 ]
Moeser, Matt [1 ,3 ]
Medvedeva, Liubov [1 ]
Martsen, Elena [1 ]
Granick, Alexander [1 ]
Raines, Lydia [1 ]
Zeng, Ming [1 ]
Makarov, Sergei, Jr. [1 ]
Houck, Keith A. [2 ]
Makarov, Sergei S. [1 ]
机构
[1] Attagene Inc, POB 12054, Res Triangle Pk, NC 27709 USA
[2] US EPA, 109 TW Alexander Dr,D343-03, Res Triangle Pk, NC 27711 USA
[3] Univ N Carolina, Lineberger Canc Res Ctr, Room 22-062, Chapel Hill, NC 27599 USA
来源
SCIENCE ADVANCES | 2018年 / 4卷 / 09期
关键词
HISTONE DEACETYLASE INHIBITORS; MITOCHONDRIAL RESPIRATION; LIVER; APOPTOSIS; RAT; ACTIVATION; TOXICITY; CELLS; CHAIN; IDENTIFICATION;
D O I
10.1126/sciadv.aar4666
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Assessing the biological activity of compounds is an essential objective of biomedical research. We show that one can infer the bioactivity of compounds by assessing the activity of transcription factors (TFs) that regulate gene expression. Using a multiplex reporter system, the FACTORIAL, we characterized cell response to a compound by a quantitative signature, the TF activity profile (TFAP). We found that perturbagens of biological pathways elicited distinct TFAP signatures in human cells. Unexpectedly, perturbagens of the same pathway all produced identical TFAPs, regardless of where or how they interfered. We found invariant TFAPs for mitochondrial, histone deacetylase, and ubiquitin/proteasome pathway inhibitors; cytoskeleton disruptors; and DNA-damaging agents. Using these invariant signatures permitted straightforward identification of compounds with specified bioactivities among uncharacterized chemicals. Furthermore, this approach allowed us to assess the multiple bioactivities of polypharmacological drugs. Thus, TF activity profiling affords straightforward assessment of the bioactivity of compounds through the identification of perturbed biological pathways.
引用
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页数:12
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