Licht T, Pastan I, Gottesman M, Herrmann F
National Cancer Institute, NIH, Laboratory of Molecular Biology, Bethesda, MD.
Ann Hematol. 1994 Oct;69(4):159-71. doi: 10.1007/BF02215949.
The multidrug transporter, P-glycoprotein (P-gp), is expressed by CD34-positive bone marrow cells, which include hematopoietic stem cells, and in other cells in the bone marrow and peripheral blood, including some lymphoid cells. Multidrug resistance mediated by P-gp appears to be a major impediment to successful treatment of acute myeloid leukemias and multiple myelomas. However, the impact of P-gp expression on prognosis has to be confirmed in several other hematopoietic neoplasms. The role of P-gp in normal and malignant hematopoiesis and clinical attempts to circumvent multidrug resistance in hematopoietic malignancies are reviewed. The recent transduction of the MDR1 gene into murine hematopoietic cells, which protects them from toxic effects of chemotherapy, suggests that MDR1 gene therapy may help prevent myelosuppression following chemotherapy.
多药转运蛋白P-糖蛋白(P-gp)由CD34阳性骨髓细胞表达,其中包括造血干细胞,也在骨髓和外周血的其他细胞中表达,包括一些淋巴细胞。P-gp介导的多药耐药似乎是急性髓性白血病和多发性骨髓瘤成功治疗的主要障碍。然而,P-gp表达对预后的影响还需在其他几种造血系统肿瘤中得到证实。本文综述了P-gp在正常和恶性造血中的作用以及临床上为规避造血系统恶性肿瘤中的多药耐药所做的尝试。最近将多药耐药1(MDR1)基因转导至小鼠造血细胞中,使其免受化疗毒性作用,这表明MDR1基因治疗可能有助于预防化疗后的骨髓抑制。