A chemical screen identifies trifluoperazine as an inhibitor of glioblastoma growth

被引:22
|
作者
Pinheiro, Tiago [1 ]
Otrocka, Magdalena [2 ]
Seashore-Ludlow, Brinton [2 ]
Rraklli, Vilma [1 ,3 ]
Holmberg, Johan [1 ,3 ]
Forsberg-Nilsson, Karin [4 ]
Simon, Andras [1 ]
Kirkham, Matthew [1 ]
机构
[1] Karolinska Inst, Dept Cell & Mol Biol, Stockholm, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, Sci Life Lab, Chem Biol Consortium Sweden, Stockholm, Sweden
[3] Karolinska Inst, Ludwig Inst Canc Res, Stockholm, Sweden
[4] Uppsala Univ, Rudbeck Lab, Sci Life Lab, Dept Immunol Genet & Pathol, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
Glioblastoma; Trifluoperazine; Dopamine; Cancer; Screening; Cell lines; STEM-CELLS; DOPAMINE; PROLIFERATION; RECEPTORS; BRAIN; DRUGS; VIVO;
D O I
10.1016/j.bbrc.2017.10.106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glioblastoma (GBM) is regarded as the most common malignant brain tumor but treatment options are limited. Thus, there is an unmet clinical need for compounds and corresponding targets that could inhibit GBM growth. We screened a library of 80 dopaminergic ligands with the aim of identifying compounds capable of inhibiting GBM cell line proliferation and survival. Out of 45 active compounds, 8 were further validated. We found that the dopamine receptor D2 antagonist trifluoperazine 2HC1 inhibits growth and proliferation of GBM cells in a dose dependent manner. Trifluoperazine's inhibition of GBM cells is cell line dependent and correlates with variations in dopamine receptor expression profile. We conclude that components of the dopamine receptor signaling pathways are potential targets for pharmacological interventions of GBM growth. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:477 / 483
页数:7
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