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亚叶酸在人淋巴细胞系中对多种抗叶酸剂的保护作用比较。

Comparison of leucovorin protection from variety of antifolates in human lymphoid cell lines.

作者信息

Browman G P, Spiegl P, Booker L, Rosowsky A

出版信息

Cancer Chemother Pharmacol. 1985;15(2):111-4. doi: 10.1007/BF00257519.

Abstract

Leucovorin requirements for protection of the T cell line CCRF-CEM and the B cell line LAZ-007 against the cytotoxic effects of a variety of antifolates were studied. Differential leucovorin protection for DDMP-induced growth suppression occurred in the opposite direction to that for MTX, with CCRF-CEM requiring less leucovorin than LAZ-007 for equivalent protection. A pattern of differential protection from DDMP different from that of protection from MTX was also seen for the cell lines RAJI and MOLT-4. Differential leucovorin protection was observed for the chain-extended MTX analogue PT441. The degree of differential protection was similar to that seen for MTX, and transport studies showed that PT441 was a weak inhibitor of tritiated MTX uptake into CCRF-CEM cells. Differential leucovorin protection was observed for the lipophilic antifolate trimetrexate glucoronate (TMQ) but the degree of differential protection was smaller than that seen for PT441 or for MTX. Since TMQ is not transported into cells by the reduced folate system, while PT441 is a weak competitive inhibitor of [3H]MTX transport, and since neither is polyglutamylated, these results support the conclusion reached in previous experiments that differential leucovorin protection of MTX is unlikely to be a transport-related phenomenon and is not due to an effect on polyglutamylation. In addition, the different patterns of relative leucovorin requirements for DDMP and MTX protection suggest that differential metabolism or catabolism of leucovorin does not account for differential protection.

摘要

研究了亚叶酸对T细胞系CCRF - CEM和B细胞系LAZ - 007的保护作用,使其免受多种抗叶酸药物的细胞毒性影响。对于DDMP诱导的生长抑制,亚叶酸的差异保护作用与甲氨蝶呤(MTX)相反,在同等保护水平下,CCRF - CEM所需的亚叶酸比LAZ - 007少。对于细胞系RAJI和MOLT - 4,也观察到了与MTX保护不同的针对DDMP的差异保护模式。对于链延长的MTX类似物PT441,观察到了差异亚叶酸保护作用。差异保护程度与MTX相似,转运研究表明PT441是氚标记的MTX进入CCRF - CEM细胞的弱抑制剂。对于亲脂性抗叶酸药物葡糖醛酸三甲曲沙(TMQ),也观察到了差异亚叶酸保护作用,但差异保护程度小于PT441或MTX。由于TMQ不能通过还原型叶酸系统转运到细胞内,而PT441是[3H]MTX转运的弱竞争性抑制剂,且两者都不会发生多聚谷氨酸化,这些结果支持了先前实验得出的结论,即MTX的差异亚叶酸保护不太可能是与转运相关的现象,也不是由于对多聚谷氨酸化的影响。此外,对于DDMP和MTX保护的相对亚叶酸需求的不同模式表明,亚叶酸的差异代谢或分解代谢不能解释差异保护现象。

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