Szakács G, Jakab K, Antal F, Sarkadi B
Membrane Research Group of the Hungarian Academy of Sciences, National Institute of Haematology and Immunology, Budapest, Hungary.
Pathol Oncol Res. 1998;4(4):251-7. doi: 10.1007/BF02905214.
Multidrug resistance (MDR), caused by the overexpression of two membrane proteins, MDR1-Pgp and/or MRP, is a major obstacle in the chemotherapy of cancer. The proper laboratory diagnosis of clinical multidrug resistance is still an unresolved question, and this uncertainty, in a vicious cycle, does not allow the correct evaluation of the clinical relevance of the MDR phenomenon. More-over, inefficient MDR diagnostics hinders the development of effective resistance-modulation strategies. In this review, after describing the basic features of the MDR drug pump proteins, the currently employed diagnostic methods are discussed. We suggest that a quantitative, functional method developed in our laboratory may provide a major help in the laboratory assessment of cancer MDR.
由两种膜蛋白MDR1-Pgp和/或MRP的过表达引起的多药耐药(MDR)是癌症化疗中的主要障碍。临床多药耐药的准确实验室诊断仍是一个未解决的问题,而这种不确定性又会恶性循环,导致无法正确评估MDR现象的临床相关性。此外,低效的MDR诊断阻碍了有效耐药调节策略的开发。在这篇综述中,在描述了MDR药物泵蛋白的基本特征之后,讨论了目前使用的诊断方法。我们认为,我们实验室开发的一种定量、功能性方法可能会在癌症MDR的实验室评估中提供很大帮助。