Jansen G, Pieters R
Department of Medical Oncology, University Hospital Vrije Universiteit, Amsterdam, The Netherlands.
Drug Resist Updat. 1998;1(3):211-8. doi: 10.1016/s1368-7646(98)80042-3.
Impaired transport appears to be a common mechanism of resistance of neoplastic cells to the antifolate methotrexate. The extensive knowledge of the molecular, biochemical and functional properties of the membrane transport systems for folates, in particular the reduced folate carrier (RFC) and membrane folate receptors (MFR), has made an important contribution to the rational design of novel antifolates that are either more efficiently internalized via these transporters or can simply bypass these transport routes. The current status of exploiting the RFC and MFR for transport of novel antifolates active in preclinical model systems and a clinical setting will be reviewed, with a special reference to childhood acute lymphoblastic leukemia (ALL) and acute non-lymphoblastic leukemia (ANLL).
转运受损似乎是肿瘤细胞对抗叶酸药物甲氨蝶呤产生耐药性的常见机制。对叶酸膜转运系统的分子、生化和功能特性,特别是还原型叶酸载体(RFC)和膜叶酸受体(MFR)的广泛了解,为合理设计新型抗叶酸药物做出了重要贡献,这些新型抗叶酸药物要么能通过这些转运体更有效地内化,要么能直接绕过这些转运途径。本文将综述利用RFC和MFR转运新型抗叶酸药物在临床前模型系统和临床环境中的活性的现状,特别提及儿童急性淋巴细胞白血病(ALL)和急性非淋巴细胞白血病(ANLL)。