Suppr超能文献

酪氨酸激酶抑制剂 E7080 和 eNOS 抑制剂 L-NIO 单独及联合应用对结直肠癌的影响。

Effects of tyrosine kinase inhibitor E7080 and eNOS inhibitor L-NIO on colorectal cancer alone and in combination.

机构信息

Department of Pharmacology, Cumhuriyet University School of Medicine, Sivas 58140, Turkey.

出版信息

Chin J Cancer Res. 2013 Oct;25(5):572-84. doi: 10.3978/j.issn.1000-9604.2013.10.10.

Abstract

OBJECTIVE

To investigate the effects of E7080 and N (5)-(1-iminoethyl)-L-ornithine dihydrochloride (L-NIO) on colorectal cancer alone and in combination.

METHODS

HT29 colorectal cancer cell line from Sap Institute was used. Real-time cell analysis (xCELLigence system) was performed to determine the effects of E7080 and L-NIO on colorectal cell proliferation. While apoptosis was determined with Annexin V staining, and the effect of agents on angiogenesis was determined with chorioallantoic membrane (CAM) model.

RESULTS

We found that E7080 has a strong antiproliferative effect with an half maximum inhibition of concentration (IC50) value of 5.60×10(-8) mol/L. Also it has been observed that E7080 showed antiangiogenic and apoptotic effects on HT29 colorectal cancer cells. Antiangiogenic scores of E7080 were 1.2, 1.0 and 0.6 for 100, 10 and 1 nmol/L E7080 concentrations, respectively. Furthermore, apoptosis has been detected in 71% of HT29 colorectal cancer cells after administration of 100 nmol/L E7080 which may indicate strong apoptotic effect. Meanwhile administration of L-NIO alone did not show any effect, but the combination of E7080 with L-NIO increased the antiproliferative, antiangiogenic and apoptotic effects of E7080.

CONCLUSIONS

Results of this study indicate that E7080 may be a good choice in treatment of colorectal tumors. Furthermore the increased effects of E7080 when combined with L-NIO raise the possibility to use a lower dose of E7080 and therefore avoid/minimize the side effects observed with E7080.

摘要

目的

研究 E7080 和 N(5)-(1-亚氨基乙基)-L-鸟氨酸二盐酸盐(L-NIO)单独及联合应用对结直肠癌细胞的作用。

方法

采用 Sap 研究所的 HT29 结直肠癌细胞系。采用实时细胞分析(xCELLigence 系统)测定 E7080 和 L-NIO 对结直肠细胞增殖的影响。用 Annexin V 染色法测定细胞凋亡,用鸡胚尿囊膜(CAM)模型测定药物对血管生成的影响。

结果

我们发现 E7080 具有很强的增殖抑制作用,半最大抑制浓度(IC50)值为 5.60×10(-8)mol/L。此外,还观察到 E7080 对 HT29 结直肠癌细胞具有抗血管生成和凋亡作用。E7080 的抗血管生成评分分别为 100、10 和 1 nmol/L E7080 浓度时为 1.2、1.0 和 0.6。此外,给予 100 nmol/L E7080 后,检测到 71%的 HT29 结直肠癌细胞发生凋亡,这可能表明其具有很强的凋亡作用。同时,单独给予 L-NIO 没有任何作用,但 E7080 与 L-NIO 联合应用增加了 E7080 的增殖抑制、抗血管生成和凋亡作用。

结论

本研究结果表明,E7080 可能是治疗结直肠肿瘤的一个较好选择。此外,E7080 与 L-NIO 联合应用增加了 E7080 的作用,这使得可以使用较低剂量的 E7080,从而避免/最小化 E7080 观察到的副作用。

相似文献

引用本文的文献

2
Arginine Metabolism and Its Potential in Treatment of Colorectal Cancer.精氨酸代谢及其在结直肠癌治疗中的潜力。
Front Cell Dev Biol. 2021 May 20;9:658861. doi: 10.3389/fcell.2021.658861. eCollection 2021.
7
The anti-angiogenic potential of (±) gossypol in comparison to suramin.(±)棉酚与苏拉明相比的抗血管生成潜力。
Cytotechnology. 2018 Dec;70(6):1537-1550. doi: 10.1007/s10616-018-0247-z. Epub 2018 Aug 19.

本文引用的文献

7
Cancer statistics, 2010.癌症统计数据,2010 年。
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
8
Paradoxical suppression of cellular senescence by p53.p53对细胞衰老的反常抑制
Proc Natl Acad Sci U S A. 2010 May 25;107(21):9660-4. doi: 10.1073/pnas.1002298107. Epub 2010 May 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验