Sonneveld P
University Hospital Rotterdam - Dijkzigt, Department of Hematology, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
J Intern Med. 2000 May;247(5):521-34.
The development of refractory disease in acute myeloid or lymphoblastic leukaemias (AML, ALL) and multiple myeloma (MM) is frequently associated with the expression of one or several multidrug resistance (MDR) genes. MDR1, MRP1 and LRP have been identified as important adverse prognostic factors in AML, T-ALL and MM. Recently, it has become possible to reverse clinical multidrug resistance by blocking P-glycoprotein-mediated drug efflux. The potential relevance of these reversal agents of MDR and potential new approaches to treat refractory disease are discussed.
急性髓细胞性或淋巴细胞性白血病(AML、ALL)以及多发性骨髓瘤(MM)中难治性疾病的发展常常与一个或多个多药耐药(MDR)基因的表达相关。MDR1、MRP1和LRP已被确定为AML、T-ALL和MM重要的不良预后因素。最近,通过阻断P-糖蛋白介导的药物外排来逆转临床多药耐药已成为可能。本文讨论了这些MDR逆转剂的潜在相关性以及治疗难治性疾病的潜在新方法。