P-GLYCOPROTEIN-MEDIATED MULTIDRUG-RESISTANCE IN NORMAL AND NEOPLASTIC HEMATOPOIETIC-CELLS

被引:59
作者
LICHT, T
PASTAN, I
GOTTESMAN, M
HERRMANN, F
机构
[1] FREE UNIV BERLIN, KLINIKUM RUDOLF VIRCHOW, ROBERT ROSSLE CANC CTR, DEPT MED ONCOL & APPL MOLEC BIOL, D-13122 BERLIN, GERMANY
[2] MAX DELBRUCK CTR MOLEC MED, D-13122 BERLIN, GERMANY
[3] NCI, DCBC, CELL BIOL LAB, BETHESDA, MD 20892 USA
[4] NCI, DCBC, MOLEC BIOL LAB, BETHESDA, MD 20892 USA
关键词
CHEMORESISTANCE; CHEMOSENSITIZING AGENTS; GENE THERAPY; MULTIDRUG RESISTANCE; P-GLYCOPROTEIN;
D O I
10.1007/BF02215949
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:159 / 171
页数:13
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