Laboratório de Hemato-Oncologia Celular e Molecular, Programa de Hemato-Oncologia Molecular, Instituto Nacional de Câncer (INCA), Rio de Janeiro, RJ, Brazil.
Laboratório de Hemato-Oncologia Celular e Molecular, Programa de Hemato-Oncologia Molecular, Instituto Nacional de Câncer (INCA), Rio de Janeiro, RJ, Brazil; Laboratório de Produtos Bioativos, Polo Novo Cavaleiros/IMCT, Campus Professor Aloisio Teixeira (UFRJ/Macaé), Universidade Federal do Rio de Janeiro (UFRJ), Macaé, RJ, Brazil.
Crit Rev Oncol Hematol. 2021 Apr;160:103281. doi: 10.1016/j.critrevonc.2021.103281. Epub 2021 Mar 2.
Acute myeloid leukemia (AML) is one of the most common hematological neoplasia causing death worldwide. The long-term overall survival is unsatisfactory due to many factors including older age, genetic heterogeneity and molecular characteristics comprising additional mutations, and resistance to chemotherapeutic drugs. The expression of ABCB1/P-glycoprotein, ABCC1/MRP1, ABCG2/BCRP and LRP transporter proteins is considered the major reason for multidrug resistance (MDR) in AML, however conflicting data have been reported. Here, we review the main issues about drug transporter proteins in AML clinical scenario, and highlight the clinicopathological significance of MDR phenotype associated with ABCB1 polymorphisms and FLT3 mutation.
急性髓细胞白血病(AML)是全球范围内导致死亡的最常见血液系统肿瘤之一。由于多种因素,包括年龄较大、遗传异质性和分子特征包括额外的突变以及对化疗药物的耐药性,长期总体生存率并不理想。ABCB1/P-糖蛋白、ABCC1/MRP1、ABCG2/BCRP 和 LRP 转运蛋白的表达被认为是 AML 多药耐药(MDR)的主要原因,但已有报道存在矛盾的数据。在这里,我们回顾了 AML 临床情况下药物转运蛋白的主要问题,并强调了与 ABCB1 多态性和 FLT3 突变相关的 MDR 表型的临床病理意义。