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吡氧噻嗪对小鼠S180移植性肿瘤的抑制作用及其对COX-2及VEGF、FGF-2、MVD表达的影响
引用本文:高雪芹,张维东,宋守芹,王丽,黄海燕.吡氧噻嗪对小鼠S180移植性肿瘤的抑制作用及其对COX-2及VEGF、FGF-2、MVD表达的影响[J].中国药理学通报,2002,18(4):426-429.
作者姓名:高雪芹  张维东  宋守芹  王丽  黄海燕
作者单位:山东省医学科学院医药生物技术中心,济南,250062,山东省医学科学院基础医学研究所,250062
摘    要:目的 探讨吡氧噻嗪对S180肉瘤细胞的抑制作用及其对肿瘤组织COX 2、VEGF、FGF 2、及微血管密度的影响。方法 昆明种小鼠随机分为对照组、FT2 0 7组、吡氧噻嗪 5、2 5、1mg·kg-1,于接种S180后d 2开始灌胃给药 ,连续 9d观察抑瘤率 ,并采用免疫组化的方法研究吡氧噻嗪对肿瘤组织COX 2及血管相关生长因子的作用。结果 吡氧噻嗪大、中、小 3个剂量组均有明显的抑瘤作用 ,抑瘤率分别为31 4 %、4 0 7%和 34 9%。免疫组化染色显示吡氧噻嗪对肿瘤组织的COX 2表达有抑制作用 ,同时血管生长相关因子VEGF、FGF 2表达也明显下调 ,MVD明显降低。结论 吡氧噻嗪对S180有抑制作用 ,它可抑制肿瘤组织COX 2的表达。COX 2表达与血管生长相关因子有关。吡氧噻嗪可通过抑制COX 2的表达而抑制肿瘤血管的生长 ,进而抑制肿瘤的生长。抑制肿瘤血管的生长可能是吡氧噻嗪预防和治疗肿瘤的又一机制

关 键 词:吡氧噻嗪  S180  环氧合酶2  血管内皮生长因子  碱性成纤维细胞生长因子  微血管密度
文章编号:1001-1978(2002)04-0426-04
修稿时间:2001年11月11

Inhibitory effects of piroxicam on the transplanted sarcoma S180 of miceand its effect on the expression of COX-2,VEGF,FGF-2 and MVD
GAO Xue Qin,ZHANG Wei Dong,SONG Shou Qin,WANG Li,HUANG Hai Yan.Inhibitory effects of piroxicam on the transplanted sarcoma S180 of miceand its effect on the expression of COX-2,VEGF,FGF-2 and MVD[J].Chinese Pharmacological Bulletin,2002,18(4):426-429.
Authors:GAO Xue Qin  ZHANG Wei Dong  SONG Shou Qin  WANG Li  HUANG Hai Yan
Abstract:AIM To investigate the effects of piroxicam on transplanted Sarcoma S180 and the expression of COX 2,VEGF,FGF 2 and microvessel density (MVD) in tumor tissue METHODS Kunming mice were randomizedly divided into control group, FT207 positive group and 5, 2 5, 1 mg·kg -1 piroxicam groups One day after inoculation of 0 2 ml S180 cell suspension, FT207 and piroxicam were given by gastric intubation for 9 days The inhibitory rate on S180 was calculated routinely The expression of COX 2,VEGF,FGF 2 and MVD was detected by immunohistochemistry RESULTS The growth of S180 was significantly inhibited by piroxicam at the doses of 5, 2 5, 1 mg·kg -1 with the inhibitory rate of 31 4%,40 7% and 34 9% respectively The expression of COX 2 in the tumor tissue was also inhibited by piroxicam. Accordingly the expression of VEGF,FGF 2 and MVD was markedly inhibited in dose dependent manner by piroxicam CONCLUSIONS The results suggest that piroxicam has inhibitory effects on S180,and it also decreases the expression of COX 2 in tumor tissue. There is a relation ship between the expression of COX 2 and angiogenesis related factor Antiangiogenesis may be another mechanism for piroxicam to exert its chemopreventive and treatment effects.
Keywords:piroxicam  sarcoma 180 cells  COX  2  VEGF  FGF  2  MVD  
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