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首页> 外文期刊>Life sciences >Chemopreventive effect of leflunomide against Ehrlich's solid tumor grown in mice: Effect on EGF and EGFR expression and tumor proliferation
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Chemopreventive effect of leflunomide against Ehrlich's solid tumor grown in mice: Effect on EGF and EGFR expression and tumor proliferation

机译:来氟米特对小鼠埃里希氏实体瘤的化学预防作用:对EGF和EGFR表达及肿瘤增殖的影响

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i) Aims: The current study aimed to examine the effect of leflunomide on tumoral expression of epidermal growth factor and its receptor (EGFR) in Ehrlich's ascites carcinoma (EAC) grown in mice. ii) Materials and methods: Mice were injected subcutaneously with EAC cells and allocated into four groups; Group i: EAC control group. Groups ii-iv: mice treated with leflunomide (3, 10 or 30 mg/kg/day, p.o.), respectively. Pharmacologic treatments were initiated at day 8 and continued for 14 days. iii) Key findings: Treatment with leflunomide evoked antitumor properties as indicated by reduction in tumor mass, histopathological score, number of intratumoral PCNA immunopositive nuclei. Leflunomide (3,10 or 30 mg/kg) exerted an anti-inflammatory effect as indicated by the reduction in serum tumor necrosis factor-alpha. Furthermore, leflunomide demonstrated anti-angiogenic activity which was expressed as a decline in serum vascular endothelial growth factor and downregulation of intratumoral EGF protein and mRNA expression as well as EGFR expression in addition to suppression of immunostaining for the endothelial marker, CD31. iv) Significance: Taken together, the present results demonstrated that leflunomide possessed anti-angiogenic and anti-proliferative activity against EAC solid tumors that might be correlated to down regulation of EGF and EGFR. Further, the current data indicated that leflunomide may have utility in the management of human cancer. (C) 2015 Elsevier Inc. All rights reserved.
机译:i)目的:目前的研究旨在检查来氟米特对小鼠生长的Ehrlich腹水癌(EAC)中表皮生长因子及其受体(EGFR)肿瘤表达的影响。 ii)材料与方法:给小鼠皮下注射EAC细胞,分为四组。组i:EAC对照组。 ii-iv组:分别用来氟米特(3、10或30mg / kg /天,口服)治疗的小鼠。药物治疗从第8天开始,持续14天。 iii)主要发现:来氟米特治疗具有抗肿瘤特性,表现为肿瘤肿块减少,组织病理学评分,肿瘤内PCNA免疫阳性核数目减少。来氟米特(3,10或30 mg / kg)发挥抗炎作用,如血清肿瘤坏死因子-α降低所表明。此外,来氟米特具有抗血管生成活性,除抑制内皮标记物CD31的免疫染色外,还表现为血清血管内皮生长因子的下降以及肿瘤内EGF蛋白和mRNA表达以及EGFR表达的下调。 iv)意义:综上所述,目前的结果表明来氟米特具有针对EAC实体瘤的抗血管生成和抗增殖活性,这可能与EGF和EGFR的下调有关。此外,当前数据表明来氟米特可能在人类癌症的治疗中具有效用。 (C)2015 Elsevier Inc.保留所有权利。

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