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Studies on drug resistance in chronic lymphocytic leukemia.

作者信息

Silber R, Potmesil M, Bank B B

机构信息

New York University School of Medicine, Department of Medicine, New York 10016.

出版信息

Adv Enzyme Regul. 1989;29:267-76. doi: 10.1016/0065-2571(89)90106-4.

DOI:10.1016/0065-2571(89)90106-4
PMID:2561248
Abstract

Chronic lymphocytic leukemia is a neoplastic disease in which drug resistance invariably occurs. We have studied the uptake and interaction with molecular targets of two drugs, chlorambucil and adriamycin, in CLL lymphocytes and CHO cell lines. Resistance does not appear related to uptake for either drug. Exposure to CLB causes DNA cross-links in the sensitive but not in the resistant cell line. The GSH content of B-CLL lymphocytes is depleted after a 20-hr incubation. An inability to maintain its GSH content may contribute to this cell's vulnerability to CLB. The resistance of CLL lymphocytes to ADR may be related to the undetectable levels of its target enzyme DNA topoisomerase II. Future approaches may involve study of novel anthracyclines, DNA topoisomerase I inhibitors and the development of in vitro predictive tests.

摘要

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引用本文的文献

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The inhibition of DNA synthesis in chronic lymphocytic leukaemia cells by chlorambucil in vitro.苯丁酸氮芥在体外对慢性淋巴细胞白血病细胞DNA合成的抑制作用。
Br J Cancer. 1992 Feb;65(2):171-6. doi: 10.1038/bjc.1992.36.
2
Mdr1/P-glycoprotein, topoisomerase, and glutathione-S-transferase pi gene expression in primary and relapsed state adult and childhood leukaemias.Mdr1/P-糖蛋白、拓扑异构酶和谷胱甘肽-S-转移酶π基因在成人及儿童白血病初发和复发状态下的表达
Br J Cancer. 1992 Sep;66(3):507-17. doi: 10.1038/bjc.1992.304.