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关于克服对甲氨蝶呤耐药性的研究:甲氨蝶呤与2,4 - 二氨基 - 5 -(3',4' - 二氯苯基)- 6 - 甲基嘧啶(BW50197)对L5178Y细胞集落形成能力影响的比较

Studies concerned with overcoming resistance to methotrexate: a comparison of the effects of methotrexate and 2,4-diamino-5-(3',4'-dichlorophenyl)-6-methylpyrimidine (BW50197) on the colony forming ability of L5178Y cells.

作者信息

Hill B T, Goldie J H, Price L A

出版信息

Br J Cancer. 1973 Sep;28(3):263-8. doi: 10.1038/bjc.1973.146.

Abstract

The effects of methotrexate (MTX) and 2,4-diamino-5-(3',4'-dichlorophenyl)-6-methylpyrimidine (BW50197) on the colony forming ability of L5178Y cells were compared. Two sub-lines of cells were used, one sensitive to methotrexate and the other resistant. In addition, the inhibitory effects of BW50197 against dihydrofolate reductase (DHFR) extracted from the MTX resistant cells were compared with those of MTX and pyrimethamine. It was found that although BW50197 was a less effective inhibitor of DHFR than MTX, it was superior to MTX at high concentrations in killing MTX resistant cells, and this superiority increased with the time of exposure to the drugs. These findings suggest that (a) when antifolate compounds are screened for antitumour activity it is insufficient simply to assess them on the basis of their ability to inhibit DHFR and (b) BW50197 should be given clinically so as to achieve the highest possible tissue concentration for the longest possible time consistent with the safety of the patient.

摘要

比较了甲氨蝶呤(MTX)和2,4-二氨基-5-(3',4'-二氯苯基)-6-甲基嘧啶(BW50197)对L5178Y细胞集落形成能力的影响。使用了该细胞的两个亚系,一个对甲氨蝶呤敏感,另一个耐药。此外,还比较了BW50197与MTX和乙胺嘧啶对从MTX耐药细胞中提取的二氢叶酸还原酶(DHFR)的抑制作用。结果发现,尽管BW50197对DHFR的抑制作用不如MTX,但在高浓度时,它在杀死MTX耐药细胞方面优于MTX,且这种优势随着药物暴露时间的延长而增加。这些发现表明:(a)在筛选抗叶酸化合物的抗肿瘤活性时,仅根据它们抑制DHFR的能力来评估是不够的;(b)临床上应给予BW50197,以便在符合患者安全的前提下,尽可能长时间地达到最高的组织浓度。

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