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胰岛素预处理可增强5-氟尿嘧啶在人食管癌细胞和结肠癌细胞中的抗癌作用。

Pretreatment with insulin enhances anticancer functions of 5-fluorouracil in human esophageal and colonic cancer cells.

作者信息

Zou Ke, Ju Ji-Hang, Xie Hong

机构信息

Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Acta Pharmacol Sin. 2007 May;28(5):721-30. doi: 10.1111/j.1745-7254.2007.00554.x.

DOI:10.1111/j.1745-7254.2007.00554.x
PMID:17439729
Abstract

AIM

To investigate the effects of insulin on enhancing 5-fluorouracil (5-FU) anticancer functions and its mechanisms in the human esophageal cancer cell line (Eca 109) and human colonic cancer cell line (Ls-174-t).

METHODS

The effect of insulin/5-FU combination treatment on the growth of Eca 109 and Ls-174-t cells was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. After insulin treatment or insulin/5-FU treatment, cell cycle distribution of both cell lines was analyzed by flow cytometry. Western blot assay was used to assess the expression of caspase-3 and thymidylate synthase (TS). Apoptosis was detected by flow cytometry, DNA fragmentation assay, and terminal transferase dUTP nick end labeling assay (TUNEL). Moreover, the changes of 5-FU uptake after insulin pretreatment were detected by HPLC assay and Western blot analysis.

RESULTS

We found that insulin enhanced the inhibitory effect of 5- FU on cell proliferation when Eca 109 cells and Ls-174-t cells were pretreated with insulin for the appropriate time. Insulin increased the cell number of the S phase and the uptake of 5-FU. Insulin/5-FU treatment enhanced apoptosis of tumor cells and upregulated the expression of cleaved caspase-3 compared with 5-FU treatment. Moreover, insulin/5-FU treatment induced the changes of free TS and the TS ternary complex level compared with 5-FU treatment in Eca 109 and Ls-174-t cells.

CONCLUSION

These data suggest that insulin enhances anticancer functions of 5- FU when it is treated before 5-FU for the appropriate time in human esophageal and colonic cancer cell lines.

摘要

目的

研究胰岛素对增强5-氟尿嘧啶(5-FU)在人食管癌细胞系(Eca 109)和人结肠癌细胞系(Ls-174-t)中的抗癌作用及其机制。

方法

采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法评估胰岛素/5-FU联合处理对Eca 109和Ls-174-t细胞生长的影响。胰岛素处理或胰岛素/5-FU处理后,通过流式细胞术分析两种细胞系的细胞周期分布。采用蛋白质免疫印迹法检测半胱天冬酶-3(caspase-3)和胸苷酸合成酶(TS)的表达。通过流式细胞术、DNA片段化分析和末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL)检测细胞凋亡。此外,通过高效液相色谱法(HPLC)和蛋白质免疫印迹分析检测胰岛素预处理后5-FU摄取的变化。

结果

我们发现,当Eca 109细胞和Ls-174-t细胞用胰岛素预处理适当时间后,胰岛素增强了5-FU对细胞增殖的抑制作用。胰岛素增加了S期细胞数量和5-FU的摄取。与5-FU处理相比,胰岛素/5-FU处理增强了肿瘤细胞凋亡并上调了裂解的caspase-3的表达。此外,与5-FU处理相比,胰岛素/5-FU处理在Eca 109和Ls-174-t细胞中诱导了游离TS和TS三元复合物水平的变化。

结论

这些数据表明,在人食管和结肠癌细胞系中,胰岛素在5-FU之前适当时间处理时可增强5-FU的抗癌作用。

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