Tanaka Takemi, De Luca Luigi M
University of Texas Health Science Center, Institute of Molecular Medicine, Houston, Texas 77030, USA.
Cancer Res. 2009 Jun 15;69(12):4945-7. doi: 10.1158/0008-5472.CAN-08-4407. Epub 2009 Jun 9.
Retinoid X receptor (RXR) is a combinatorial partner for one third of the 48 human nuclear receptor superfamily members and acts as a master coordinator of nuclear receptor signaling pathways involved in the control of cell growth and differentiation. Thus, ligand-dependent simultaneous activation of multiple pathways is an attractive strategy for molecular-targeted therapy of neoplastic disease. However, clinical trials in RXR-targeted molecular therapy with the RXR ligand (rexinoid) have yielded disappointing outcomes. In this review, we discuss a possible mechanism underlying the loss of sensitivity to rexinoid therapy.
维甲酸X受体(RXR)是48种人类核受体超家族成员中三分之一成员的组合伴侣,并且在参与细胞生长和分化控制的核受体信号通路中充当主要协调者。因此,配体依赖性的多途径同时激活是肿瘤疾病分子靶向治疗的一种有吸引力的策略。然而,使用RXR配体(类视黄醇)进行的RXR靶向分子治疗的临床试验产生了令人失望的结果。在本综述中,我们讨论了对类视黄醇治疗敏感性丧失的潜在机制。