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5'-脱氧-5-氟尿苷与L-半胱氨酸口服联合给药增强抗肿瘤作用。

Enhanced antitumor effect of 5'-deoxy-5-fluorouridine by oral administration with L-cysteine.

作者信息

Iigo M, Nakajima Y, Araki E, Hoshi A

机构信息

Chemotherapy Division, National Cancer Center Research Institute, Tokyo.

出版信息

Jpn J Cancer Res. 1989 Feb;80(2):182-7. doi: 10.1111/j.1349-7006.1989.tb02287.x.

Abstract

When given orally in combination with L-cysteine, 5'-deoxy-5-fluorouridine (DFUR) brought about a significant reduction in the growth of adenocarcinoma 755 and a significant prolongation of life-span in mice bearing Lewis lung carcinoma without increased toxicity to the host as compared with DFUR alone, though L-cysteine alone did not show an appreciable antitumor activity. Moreover, the combination of DFUR and L-cysteine resulted in a marked retardation of growth of human colon tumor LS174T transplanted into nude mice. Thus, the potency of DFUR was increased by L-cysteine. Pharmacokinetic studies revealed that after DFUR administration, plasma DFUR and 5-fluorouracil (5-FU) levels rapidly declined, but that, in the combination with L-cysteine, the plasma clearances of DFUR and 5-FU were slowed down considerably. In the tumor, DFUR and 5-FU levels were similar to those in the plasma. Such a prolongation of DFUR and 5-FU levels in plasma and tumor may produce the enhancement of antitumor effect seen with the combination of DFUR and L-cysteine.

摘要

当与L-半胱氨酸联合口服给药时,5'-脱氧-5-氟尿苷(DFUR)使腺癌755的生长显著降低,并使携带Lewis肺癌的小鼠寿命显著延长,与单独使用DFUR相比,对宿主的毒性并未增加,尽管单独的L-半胱氨酸未显示出明显的抗肿瘤活性。此外,DFUR与L-半胱氨酸的组合导致移植到裸鼠体内的人结肠肿瘤LS174T的生长明显迟缓。因此,L-半胱氨酸增强了DFUR的效力。药代动力学研究表明,给予DFUR后,血浆中DFUR和5-氟尿嘧啶(5-FU)水平迅速下降,但与L-半胱氨酸联合使用时,DFUR和5-FU的血浆清除率显著减慢。在肿瘤中,DFUR和5-FU水平与血浆中的相似。血浆和肿瘤中DFUR和5-FU水平的这种延长可能产生了DFUR与L-半胱氨酸联合使用时所见的抗肿瘤作用增强。

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Mechanism of potentiation of antitumor activity of 5-fluorouracil against adenocarcinoma 755 by L-cysteine.
Biochem Pharmacol. 1986 Mar 1;35(5):727-30. doi: 10.1016/0006-2952(86)90238-8.

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