Pinheiro Tiago, Otrocka Magdalena, Seashore-Ludlow Brinton, Rraklli Vilma, Holmberg Johan, Forsberg-Nilsson Karin, Simon András, Kirkham Matthew
Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Chemical Biology Consortium Sweden, Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Biochem Biophys Res Commun. 2017 Dec 16;494(3-4):477-483. doi: 10.1016/j.bbrc.2017.10.106. Epub 2017 Oct 21.
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 2HCl 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.
胶质母细胞瘤(GBM)被认为是最常见的恶性脑肿瘤,但治疗选择有限。因此,对于能够抑制GBM生长的化合物和相应靶点存在未满足的临床需求。我们筛选了一个包含80种多巴胺能配体的文库,旨在鉴定能够抑制GBM细胞系增殖和存活的化合物。在45种活性化合物中,有8种进一步得到验证。我们发现多巴胺受体D2拮抗剂盐酸三氟拉嗪以剂量依赖性方式抑制GBM细胞的生长和增殖。三氟拉嗪对GBM细胞的抑制作用具有细胞系依赖性,并且与多巴胺受体表达谱的变化相关。我们得出结论,多巴胺受体信号通路的成分是GBM生长药理学干预的潜在靶点。