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1
Kinetic analysis of 5-fluorouracil action against various cancer cells.5-氟尿嘧啶对多种癌细胞作用的动力学分析。
Jpn J Cancer Res. 1990 Oct;81(10):1039-44. doi: 10.1111/j.1349-7006.1990.tb03343.x.
2
Somatostatin analogue octreotide modulates metabolism and effects of 5-fluorouracil and 5-fluorouridine in human colon cancer spheroids.生长抑素类似物奥曲肽调节人结肠癌球体中5-氟尿嘧啶和5-氟尿苷的代谢及作用。
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Correlation between ribosomal RNA production and RNA-directed fluoropyrimidine cytotoxicity.
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Effect of guanosine on antitumor activity of fluorinated pyrimidines against P 388 leukemia.
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Modulation of 1-beta-D-arabinofuranosylcytosine metabolism and cytotoxicity in L1210 cells by fluoropyrimidine pretreatment.氟嘧啶预处理对L1210细胞中1-β-D-阿拉伯呋喃糖基胞嘧啶代谢及细胞毒性的调节作用。
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Flow cytometric analysis of cell-killing actions of 5-fluorouracil in human colorectal cancer cells.
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On the mechanism of cytotoxicity of fluorinated pyrimidines in four human colon adenocarcinoma xenografts maintained in immune-deprived mice.关于氟嘧啶对免疫缺陷小鼠体内四种人结肠腺癌异种移植瘤的细胞毒性作用机制
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Mechanism for resistance to 5-fluorouracil in P388 leukemia cells.
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Evaluation of plasma 5-fluorouracil nucleoside levels in patients with metastatic breast cancer: relationships with toxicities.转移性乳腺癌患者血浆5-氟尿嘧啶核苷水平的评估:与毒性的关系。
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5-Fluorouracil induces apoptosis in human colon cancer cell lines with modulation of Bcl-2 family proteins.5-氟尿嘧啶通过调节Bcl-2家族蛋白诱导人结肠癌细胞系凋亡。
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Increased sensitivity to long-term 5-fluorouracil exposure of human colon cancer HT-29 cells resistant to short-term exposure.对短期暴露具有抗性的人结肠癌HT - 29细胞对长期5 - 氟尿嘧啶暴露的敏感性增加。
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9
Pharmacological effects of 5-fluorouracil microspheres on peritoneal carcinomatosis in animals.5-氟尿嘧啶微球对动物腹膜癌病的药理作用
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Reduced activity of anabolizing enzymes in 5-fluorouracil-resistant human stomach cancer cells.5-氟尿嘧啶耐药的人胃癌细胞中合成代谢酶活性降低。
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本文引用的文献

1
Biochemical determinants of responsiveness to 5-fluorouracil and its derivatives in xenografts of human colorectal adenocarcinomas in mice.小鼠体内人大肠腺癌异种移植瘤对5-氟尿嘧啶及其衍生物反应性的生化决定因素
Cancer Res. 1981 Jan;41(1):144-9.
2
5-Fluorouracil incorporation into human breast carcinoma RNA correlates with cytotoxicity.5-氟尿嘧啶掺入人乳腺癌RNA与细胞毒性相关。
J Biol Chem. 1981 Oct 10;256(19):9802-5.
3
Association of cell lethality with incorporation of 5-fluorouracil and 5-fluorouridine into nuclear RNA in human colon carcinoma cells in culture.培养的人结肠癌细胞中细胞致死率与5-氟尿嘧啶和5-氟尿苷掺入核RNA的相关性。
Mol Pharmacol. 1982 Mar;21(2):468-73.
4
Effect of excess folates and deoxyinosine on the activity and site of action of 5-fluorouracil.过量叶酸和脱氧肌苷对5-氟尿嘧啶活性及作用位点的影响。
Cancer Res. 1981 Sep;41(9 Pt 1):3288-95.
5
Treatment of cultured human colon carcinoma cells with fluorinated pyrimidines.用氟嘧啶处理培养的人结肠癌细胞。
Cancer. 1980 Mar 15;45(5 Suppl):1144-58. doi: 10.1002/1097-0142(19800315)45:5+<1144::aid-cncr2820451319>3.0.co;2-p.
6
Thymidylate synthetase inhibition in malignant tumors and normal liver of patients given intravenous 5-fluorouracil.接受静脉注射5-氟尿嘧啶的患者恶性肿瘤和正常肝脏中胸苷酸合成酶的抑制作用
Cancer Res. 1984 Sep;44(9):4144-50.
7
Relationship of cellular folate cofactor pools to the activity of 5-fluorouracil.细胞叶酸辅助因子库与5-氟尿嘧啶活性的关系。
Mol Pharmacol. 1983 Jan;23(1):190-7.
8
Relationship of dUMP and free FdUMP pools to inhibition of thymidylate synthase by 5-fluorouracil.脱氧尿苷一磷酸(dUMP)和游离氟脱氧尿苷一磷酸(FdUMP)池与5-氟尿嘧啶对胸苷酸合成酶抑制作用的关系
Mol Pharmacol. 1984 Mar;25(2):303-9.
9
Lethality associated with incorporation of 5-fluorouracil into preribosomal RNA.5-氟尿嘧啶掺入前核糖体RNA相关的致死性。
Mol Pharmacol. 1984 Jul;26(1):135-40.
10
On the mechanism of cytotoxicity of fluorinated pyrimidines in four human colon adenocarcinoma xenografts maintained in immune-deprived mice.关于氟嘧啶对免疫缺陷小鼠体内四种人结肠腺癌异种移植瘤的细胞毒性作用机制
Cancer. 1980 Mar 15;45(5 Suppl):1159-67. doi: 10.1002/1097-0142(19800315)45:5+<1159::aid-cncr2820451320>3.0.co;2-z.

5-氟尿嘧啶对多种癌细胞作用的动力学分析。

Kinetic analysis of 5-fluorouracil action against various cancer cells.

作者信息

Inaba M, Mitsuhashi J, Ozawa S

机构信息

Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo.

出版信息

Jpn J Cancer Res. 1990 Oct;81(10):1039-44. doi: 10.1111/j.1349-7006.1990.tb03343.x.

DOI:10.1111/j.1349-7006.1990.tb03343.x
PMID:2146239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5917971/
Abstract

Based on our recent kinetic analysis, which made it possible to distinguish between the cell-killing actions of cell cycle phase-specific and non-specific agents, we attempted to elucidate the actions of 5-fluorouracil (FUra) on three different cancer cell lines. By colony-forming assay, the concentrations of fluorouridine (FUrd), fluorodeoxyuridine (FdUrd) or FUra giving 90% cell kill (IC90) at various exposure times (texps) were obtained. With P388 cells, the curve of texps-IC90 for FUrd on a log-log scale was linear with a slope of -1, which is typical for cell cycle phase-nonspecific agents. In contrast, the curve for FdUrd showed a much steeper slope than -1, which is characteristic for cell cycle phase-specific agents. We found that the curve for FUra was exactly the same as that for FUrd, indicating that the mode of FUra action on P388 leukemia is analogous to that of FUrd. Similar results were observed with human colon and renal cancer cell lines, HT-29 and KU-2, although when the cells were exposed to relatively low concentrations of FUra for a long time, a cell cycle phase-specific action became evident.

摘要

基于我们最近的动力学分析,该分析能够区分细胞周期特异性和非特异性药物的细胞杀伤作用,我们试图阐明5-氟尿嘧啶(FUra)对三种不同癌细胞系的作用。通过集落形成试验,获得了在不同暴露时间(texps)下导致90%细胞杀伤(IC90)的氟尿苷(FUrd)、氟脱氧尿苷(FdUrd)或FUra的浓度。对于P388细胞,FUrd在对数-对数尺度上的texps-IC90曲线是线性的,斜率为-1,这是细胞周期非特异性药物的典型特征。相比之下,FdUrd的曲线显示出比-1更陡的斜率,这是细胞周期特异性药物的特征。我们发现FUra的曲线与FUrd的曲线完全相同,表明FUra对P388白血病的作用模式与FUrd类似。在人结肠癌细胞系HT-29和肾癌细胞系KU-2中也观察到了类似的结果,尽管当细胞长时间暴露于相对较低浓度的FUra时,细胞周期特异性作用变得明显。