Benod Cindy, Villagomez Rosa, Webb Paul
Department of Genomic Medicine, Houston Methodist Research Institute (HMRI), 6670 Bertner Avenue, Houston, TX 77030, USA.
Department of Genomic Medicine, Houston Methodist Research Institute (HMRI), 6670 Bertner Avenue, Houston, TX 77030, USA.
J Steroid Biochem Mol Biol. 2016 Mar;157:41-7. doi: 10.1016/j.jsbmb.2015.11.001. Epub 2015 Nov 10.
TLX (tailless receptor) is a member of the nuclear receptor superfamily and belongs to a class of nuclear receptors for which no endogenous or synthetic ligands have yet been identified. TLX is a promising therapeutic target in neurological disorders and brain tumors. Thus, regulatory ligands for TLX need to be identified to complete the validation of TLX as a useful target and would serve as chemical probes to pursue the study of this receptor in disease models. It has recently been proved that TLX is druggable. However, to identify potent and specific TLX ligands with desirable biological activity, a deeper understanding of where ligands bind, how they alter TLX conformation and of the mechanism by which TLX mediates the transcription of its target genes is needed. While TLX is in the process of escaping from orphanhood, future ligand design needs to progress in parallel with improved understanding of (i) the binding cavity or surfaces to target with small molecules on the TLX ligand binding domain and (ii) the nature of the TLX coregulators in particular cell and disease contexts. Both of these topics are discussed in this review.
无尾受体(TLX)是核受体超家族的成员,属于一类尚未鉴定出内源性或合成配体的核受体。TLX是神经疾病和脑肿瘤中一个有前景的治疗靶点。因此,需要鉴定TLX的调节性配体,以完成将TLX验证为有用靶点的工作,并且这些配体可作为化学探针用于在疾病模型中研究该受体。最近已证明TLX是可成药的。然而,为了鉴定具有理想生物活性的强效且特异性的TLX配体,需要更深入地了解配体的结合位置、它们如何改变TLX构象以及TLX介导其靶基因转录的机制。虽然TLX正逐渐摆脱“孤儿受体”的身份,但未来的配体设计需要与对以下两方面的深入理解同步进行:(i)TLX配体结合域上用于小分子靶向的结合腔或表面;(ii)在特定细胞和疾病背景下TLX共调节因子的性质。本综述将对这两个主题进行讨论。