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三肽化合物酪丝亮肽抗肿瘤作用及对单核巨噬细胞激活作用机制
Anti-Tumor Effects of Tripeptide Tyroserleutide and Its Mechanisms by Activating Monocyte-Macrophages
【摘要】 目的:观察三肽化合物酪丝亮肽的抗肿瘤作用,探讨其对单核巨噬细胞的激活作用。方法:观察YSL对人肝癌BEL-7402裸鼠移植瘤的抑制作用;观察YSL对体外培养。BEL-7402细胞体系的抑制作用;观察YSL对PEMφ杀伤肿瘤细胞BEL-7402及B16-F10的影响;观察YSL对PEMφ分泌合成IL-1β,FNF-α和NO等细胞毒效应分子的影响。结果:YSL能显著抑制BEL-7402移植瘤裸鼠的肿瘤生长,给药剂量为160μg/(kg·d)时疗效最显著,抑制率为44.03%;YSL体外对BEL-7402细胞生长有一定的抑制作用,与阴性对照组比较有显著性差异(P<0.05);YSL能增强裸鼠PEMφ对BEL-7402,B16-F10杀伤作用,与生理盐水对照组相比有显著性差异(P<0.05);YSL能增强Balb/c小鼠PEMφ对BEL-7402,B16-F10杀伤作用,与生理盐水对照组相比有显著性差异(P<0.05);YSL能促进小鼠PEMφ分泌合成细胞毒效应分子IL-1β,TNF-α和NO,与生理盐水对照组相比有显著性差异(P<0.05)。结论:YSl能够抑制BEL-7402的增殖,增强单核巨噬细胞的细胞毒功能,促进细胞霉效应分子IL-1β,TNF-α和NO的分泌合成。
【Abstract】 Objective:To investigate the anti-tumor effects of the tripeptide tyroserleutide (YSL) and to discuss its mechanisms by activating monocyte-macrophages. Methods:To apply human hepatocarcinoma BEL-7402 tumor transplanted in nude mice to examine the anti-tumor effects of YSL. To apply human hepatocarcinoma cell BEL-7402 to investigated the cytotoxicity of YSL against human hepatocarcinoma BEL-7402 cell line in vitro. To explore the activating effects of YSL on the peritoneal macrophage (PEMφ) functions of cytotoxicity against tumor cell lines (BEL-7402,B16-F10) in vitro and to detected the effects of YSL on the content of cytotoxicity effectors IL-1β,TNF-α and NO produced by PEMφ. Results:YSL could inhibit the growth of transplanted tumor BEL-7402 in nude mice, the inhibition rate of 160μg/(kg·d) was 44.03%. The tumoricidal activity of YSL against BEL-7402 cell line in vitro was observed when compared with the control group (P< 0.05).YSL could activated PEMφ of nude mice and markedly enhance cytotoxicity against tumor cel lines (BEL-7402, B16-F10) when compared with the control group (P<0.05). YSL could activated PEMφ of Balb/c mice and marked enhance cytotoxicity against tumor cell lines (BEL-7402, B16-F10) when compared with producing group (P<0. 05).YSL could stimulate the contents of the cytotoxicity effectors of IL-1β,TNF-α and NO produced by PEMφ(P<0.05). Conclusions:YSL had inhibition functions against human hepatocarcinoma BEL-7402. YSL could increase the cytotoxicity of mono-cyte-macrophages and stimulate producing of the contents of the cytotoxicity effector of IL-1β,TNF-α and NO.
【Key words】 tyroserleutide; human hepatocarcinoma BEL-7402; macrophage; cytotoxicity effectors;
- 【文献出处】 中国肿瘤生物治疗杂志 ,Chinese Journal of Cancer Biotherapy , 编辑部邮箱 ,2005年02期
- 【分类号】R73-3
- 【被引频次】12
- 【下载频次】187