Molina-Arcas M, Marcé S, Villamor N, Huber-Ruano I, Casado F J, Bellosillo B, Montserrat E, Gil J, Colomer D, Pastor-Anglada M
Departament de Bioquímica i Biologia Molecular, Universitat de Barcelona, E-08028 Barcelona, Spain.
Leukemia. 2005 Jan;19(1):64-8. doi: 10.1038/sj.leu.2403582.
Fludarabine is considered the treatment of choice for most patients with chronic lymphocytic leukemia (CLL). We have analyzed the role of plasma membrane transporters in nucleoside-derived drug bioavailability and action in CLL cells. Among the known plasma membrane transporters, we have previously observed a significant correlation between fludarabine uptake via ENT carriers and ex vivo sensitivity of CLL cells to fludarabine, although mRNA amounts of the equilibrative nucleoside transporters hENT1 and hENT2 do not show any predictive response to treatment. In this study, using polyclonal monospecific antibodies we have observed a significant correlation between the expression of hENT2 by Western blot and fludarabine uptake via hENT carriers and also with ex vivo sensitivity of CLL cells to fludarabine. These results suggest that the equilibrative nucleoside transporter hENT2 plays a role in fludarabine responsiveness in CLL patients.
氟达拉滨被认为是大多数慢性淋巴细胞白血病(CLL)患者的首选治疗药物。我们分析了质膜转运蛋白在核苷衍生药物生物利用度及对CLL细胞作用中的作用。在已知的质膜转运蛋白中,我们之前观察到通过ENT载体摄取氟达拉滨与CLL细胞对氟达拉滨的体外敏感性之间存在显著相关性,尽管平衡核苷转运蛋白hENT1和hENT2的mRNA量对治疗未显示出任何预测反应。在本研究中,使用多克隆单特异性抗体,我们通过蛋白质印迹观察到hENT2的表达与通过hENT载体摄取氟达拉滨之间存在显著相关性,并且与CLL细胞对氟达拉滨的体外敏感性也存在显著相关性。这些结果表明,平衡核苷转运蛋白hENT2在CLL患者对氟达拉滨的反应中发挥作用。