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作 者:田原僮[1] 曾昭毅[1] 陈伟伟[1] 何蔚[1] 赵丽娟[2]
机构地区:[1]赣南医学院药理学教研室,江西赣州341000 [2]吉林大学白求恩医学院病理生理学教研室,吉林长春130021
出 处:《中国药理学通报》2009年第11期1449-1452,共4页Chinese Pharmacological Bulletin
基 金:科技部国际科技合作重点项目(No2004DFB02000)
摘 要:目的探讨聚肌胞(polvriboinsine-polyribocyaidylic acid,polyI:C)对小鼠前列腺癌组织内血管生成的影响,初探其可能机制。方法将16只C57BL6/J纯系荷瘤小鼠按瘤重随机分为对照组和polyI:C组,分别瘤内注射生理盐水和polyI:C(每3d1次),用药7次后切除瘤灶。HE染色,镜下观察肿瘤组织组织形态学变化及血管分布情况。利用试剂盒检测肿瘤组织内NO水平。免疫组织化学染色,观察肿瘤组织eNOS、VEGF和AQP1蛋白表达情况。结果对照组和polyI:C组小鼠前列腺癌组织内的NO含量分别为(8.73±5.34)μmol和(1.22±0.77)μmol,两组比较差异有显著性(P<0.05)。免疫组化结果显示,对照组和polyI:C组的VEGF阳性染色前列腺癌细胞计数占同类肿瘤细胞的比例分别为(37.91±7.62)%和(9.64±2.90)%;C组的eNOS阳性染色前列腺癌细胞计数占同类肿瘤细胞的比例分别为(54.43±10.39)%和(22.00±8.07)%;AQP1平均值分别为(14.8±3.5)和(3.2±1.3),两组比较差异有显著性(P<0.05)。结论polyI:C可能通过下调小鼠前列腺癌组织中eNOS和VEGF蛋白的表达,抑制小鼠前列腺癌组织内血管的生成;通过影响组织内AQP1蛋白水平、减少NO生成和释放,影响血管内皮细胞的功能和肿瘤组织的微循环。Aim To investigate the effects of polyI:C on angiogenesis in mouse prostate carcinoma and its mechanisms.Methods Prostate carcinoma bearing mice were randomly divided into two groups according to tumor volume:contrl group and polyI:C group.After seven times′treatment,the mice were sacrificed.The content of NO in tumor was measured by nitric oxide assay kit.Tumor tissues were partly performed hematoxylin-eosin staining to observe morphological changes and distribution of vasa.Immunohisto chemical staining was used to observe the expression of VEGF,eNOS and AQP1.Results The content of NO in polyI:C group and the control was(1.22±0.77)μmol and(8.73±5.34)μmol respectively,and there was significant difference between two groups(P0.05).The expression of VEGF in polyI:C group and the control was (9.64±2.90)% and(37.91±7.62)% respectively,and there was significant difference between two groups(P0.01).The expression of eNOS in polyI:C group and the control was(22.00±8.07)% and (54.43±10.39)% respectively,and there was significant difference between two groups(P0.01).The mean expression of AQP1 in polyI:C group and the control was(3.2±1.3) and (14.8±3.5) respectively,and there was significant difference between two groups(P0.05).Conclusions Through downregulation the expression of VEGF and eNOS,polyI:C plays an important role in inhibiting angiogenesis of mouse prostate carcinoma.By reducing the expression of AQP1 and the content of NO,it influences endothelial cell function and local tumor microcirculation.
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