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安替可胶囊对Lewis肺癌小鼠肿瘤抑制作用及其抗血管生成作用的实验研究 被引量:4

The effects of Antike capsule in the treatment of Lewis lung cancer mice and its influence on the anti-angiogenesis effects in mice
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摘要 目的:探讨安替可胶囊对Lewis肺癌小鼠的肿瘤抑制作用及其抗血管生成作用。方法:将40只C57BL/6小鼠分为模型组、阳性药组[索拉非尼0.16g/(kg·d)、低剂量组0.27g/(kg·d)及高剂量组0.54g/(kg·d)]。接种Lewis细胞进行造模,成功后对各组灌胃给予安替可,连续14d。末次给药24h后,观察各组体重、肿瘤体积、重量与肿瘤生长抑制率。对小鼠肿瘤组织进行病理组织学观测,并观察血管内皮生长因子(VEGF)、金属肽酶含血小板反应蛋白1(ADAMTS1)、低氧诱导因子-1α(HIF-1α)及血管内皮生长因子受体-2(VEGFR-2)免疫荧光染色表达量。结果:与模型组比较,低、高剂量组肿瘤体积与重量均明显降低,且体重明显增高(P<0.05),肿瘤生长抑制率分别为50.0%及40.6%。与模型组比较,高、低剂量组肿瘤组织中均可见不同程度的癌细胞出现坏死与凋亡。免疫荧光染色结果则表明,高、低剂量组VEGF、VEGFR-2、ADAMTS1及HIF-1α蛋白的相对表达量均明显优于模型组(P<0.05)。结论:安替可胶囊对Lewis肺癌小鼠具有较好的肿瘤抑制作用,其主要机制可能为抗血管生成活性。 Objective:To observe the effects of antike capsule in the treatment of Lewis lung cancer mice and its influence on the anti-angiogenesis effects in mice.Methods:40 Lewis lung cancer mice were divided into control group,sorafenib group[0.16 g/(kg·d)],high dose group[0.54 g/(kg·d)]and low dose group[0.27 g/(kg·d)].Using lewis lung cancer cells axillary vaccination to build the model,after the model built,the antike was gavaged for 14 days.24 h after the last gavage,the body weight,tumor volume and weight,tumor growth inhibition percent were observed.The histopathologies were observed in the mice,while immunofluorescent staining of VEGF,ADAMTS1,HIF-1αand VEGFR-2 were detected in the groups.Results:Compared with the model group,the body weight,the tumor volume and weight were significantly lower in high and low dose groups(P<0.05),while tumor growth inhibition percents were 50.0%and 40.6%.Pathological observations showed that the tumor cells in the high and low dose group were significantly necrosis and apoptosis in the tumor tissue than model group.Immunofluorescent staining shown,the expression of VEGF,ADAMTS1,HIF-1αand VEGFR-2 were significantly promoted in the high and low dose group than the model group(P<0.05).Conclusion:Antike capsule in the treatment of lewis lung cancer mice were effective,and have good anti-angiogenesis effects in mice.
作者 马薇 舒庆 周丹 赵小燕 付联强 马岩敏 Ma Wei;Shu Qing;Zhou Dan(Department of Pharmacy,Ninth Hospital of Xi’an,Xi’an 710054)
出处 《陕西医学杂志》 CAS 2018年第2期147-149,共3页 Shaanxi Medical Journal
关键词 肺肿瘤/药物疗法 抗肿瘤药/治疗应用 小鼠 分子药理作用机制 @安替可胶囊 Lung neoplasms/drug therapy Antineoplastic agents/therapeutic use Mice Molecular mechanisms of pharmacological action @Antike capsule
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  • 1孙秋艳,刘艳,汪茜,刘洁,包旭.绿原酸对Lewis肺癌小鼠及人A549肺癌的实验研究[J].华西药学杂志,2010,25(5):536-538. 被引量:21
  • 2王四旺,谢艳华.安替可胶囊对人癌细胞抑制的作用[J].第四军医大学学报,1996,17(4):283-286. 被引量:10
  • 3胡家柱,谢方云,曹小龙,毛志达.放疗结合安替可胶囊治疗Ⅱ~Ⅳ期鼻咽癌的临床观察[J].国际医药卫生导报,2006,12(11):4-5. 被引量:3
  • 4蔡光蓉,李佩文,潘敏求,等.安替可治疗中晚期原发性肝癌137例[C].第十届全国中西医结合肿瘤学术大会论文汇编,2006:230-231.
  • 5王四旺,谢艳华,朱玲珍.安替可胶囊抗肿瘤作用的机理[J].第四军医大学学报,1997,18(4):368-368. 被引量:17
  • 6Xu XY, Glenn D. Inhibition of tumor growth and angiogenesis by a lysophosphatidie acid antagonist in an engineered three-dimen- sional lung cancer xenograft model[J]. Cancer, 2010, 116(7) : 1739 - 1750.
  • 7Meuwissen R, Berns A. Mouse models for human lung cancer [ J]. Genes Dev, 2005,19:643 - 664.
  • 8Jonkem J, Berns A. Conditional mouse models of sporadic cancer [J]. Nat Rev Cancer, 2002, 2(4) :251 -265.
  • 9Kesharnouni VG, Reddy RC, Arenberg DA, et al. Peroxisome proliferator-activated receptor-gamma activation inhibits tumor progression in non-small-cell lung cancer[J]. Oncogene, 2004, 23(1) :100 - 108.
  • 10Zou Y, Fu H, Ghosh S, et al. Antitumor activity of hydrophilic Paclitaxel copolymer prodrug using locoregional delivery in human orthotopic non-smaU cell lung cancer xenograft models [ J]. Clin Cancer Res, 2004, 10(21) :7382 -7391.

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