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培哚普利抗S180肉瘤生长的实验研究[J]. 肿瘤防治研究, 2011, 38(05): 515-518. DOI: 10.3971/j.issn.1000-8578.2011.05.009
引用本文: 培哚普利抗S180肉瘤生长的实验研究[J]. 肿瘤防治研究, 2011, 38(05): 515-518. DOI: 10.3971/j.issn.1000-8578.2011.05.009
Experiment Research on Anti-tumor Effects of Perindopril on S180 Tumor[J]. Cancer Research on Prevention and Treatment, 2011, 38(05): 515-518. DOI: 10.3971/j.issn.1000-8578.2011.05.009
Citation: Experiment Research on Anti-tumor Effects of Perindopril on S180 Tumor[J]. Cancer Research on Prevention and Treatment, 2011, 38(05): 515-518. DOI: 10.3971/j.issn.1000-8578.2011.05.009

培哚普利抗S180肉瘤生长的实验研究

Experiment Research on Anti-tumor Effects of Perindopril on S180 Tumor

  • 摘要: 目的探讨培哚普利抗S180肉瘤生长的作用及其相关机制。方法采用S180小鼠移植瘤模型,将小白鼠随机分为3组,分别给予蒸馏水、培哚普利(0.50 mg/ml)、血管紧张素Ⅱ(0.25 mg/ml)灌胃10天,期间称取小鼠体重,绘制体重均数变化曲线,并观察小鼠的一般状况及进食情况。第11天处死小鼠,称体重、瘤重,计算抑瘤率。通过HE、免疫组织化学染色,观察肿瘤组织结构及MVD、VEGF、AngⅡ的表达情况。结果各组小鼠体重均有增加,但各组体重差别无统计学意义(P>0.05);与对照组相比,血管紧张素Ⅱ组肿瘤生长显著增大(P<0.05),培哚普利组肿瘤生长受到显著抑制(P<0.05);培哚普利组肿瘤组织MVD、VEGF、AngⅡ表达强度均显著低于对照组(P<0.05),而血管紧张素Ⅱ组肿瘤组织MVD、VEGF表达强度均显著高于对照组(P<0.05)。结论培哚普利能显著抑制S180肉瘤生长,其机制可能与降低肿瘤组织AngⅡ、VEGF、MVD的表达、从而抑制肿瘤血管生成有关。

     

    Abstract: ObjectiveTo investigate the anti-tumor effects of perindopril on growth of S180 tumor in mice. Methods The mice loaded S180 cell line were randomly divided into 3 groups.The perindopril (0.50 mg/ml) angiotensin Ⅱ (AngⅡ 0.25 mg/ml) and sistilled water(blank control)were administered by gavage daily for 10 days.The anti-tumor effects of perindopril were evaluated by body weight, food-intake and tumor weight.MVD,VEGF,AngⅡ expression were detected by HE and immunohistochemical staining. Results The mice body weights were increased obviously, and no significant difference among three groups(P>0.05 ). Compared with control group, tumor growth of perindorpril (0.50mg/ml)group was remarkably inhibited(P<0.05), and AngⅡ group was remarkably increased(P<0.05).MVD, VEGF, AngⅡ expressions were decreased in perindorpril(0.50mg/ml) group. MVD and VEGF expressions were increased in AngⅡ group(0.25mg/ml) (P<0.05). Conclusion The perindorpril was able to significantly inhibit the growth of S180 tumor throngh inhibiting tumor angiogenesis induced by AngⅡ, VEGF and MVD down-regulation.

     

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