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作 者:郭晓钟[1] 田宏[1] 徐建华[1] 弭延斌[1] 崔忠敏[1] 李宏宇[1] 张巍巍[1] 赵佳军[1] 穆振斌[1]
出 处:《中华消化杂志》2008年第3期175-178,共4页Chinese Journal of Digestion
基 金:国家自然科学基金资助项目(30470798)
摘 要:目的研究肿瘤转移抑制基因Kangai-1(KAI1)对胰腺癌细胞增殖功能及转移潜能的影响。方法建立经腺病毒(Ad)成功构建的重组载体(Ad—KAI1),并转染胰腺癌PANCI细胞。用血管内皮生长因子(VEGF)和表皮生长因子(EGF)作为诱导剂,按照不同诱导时间点(3、5、7h)将PANCI细胞进行实验分组,比较感染前后细胞形态。采用Transwell方法对PANCI细胞转染Ad—KAI1前、后的迁移作用进行比较。采用免疫细胞化学法检测细胞粘附分子-1(ICAM-1)和金属蛋白酶-9(MMP-9)在PANCI细胞转染Ad—KAI1前、后的表达水平。结果在VEGF和EGF诱导下,转染Ad—KAI1后与转染前相比,PANCI细胞的迁移能力明显下降(P〈0.05)。免疫细胞化学研究提示,PANCI细胞中ICAM-1、MMP-9均呈阳性表达,转染后均呈阴性表达。结论KAI1基因抑制胰腺癌转移可能是通过抑制ICAM-1和MMP-9的表达。Objective To investigate the underlying mechnisms of Kangai-l(KAI1) gene, a tumor metastasis suppressor gene, on metastasis and prolification of pancreatic cancer cells. Methods The plasmin containing Ad-KAI1 was established and transfected into pancreatic cancer cell line PCNA I. The PCNA I cells were then divided into different groups according to the times induced by vascular endothelial growth factor(VEGF) and epidermal growth factor(EGF). The morphology and migrational ability of PANC I cells were compared before and after transfection by microscopy and transwell method, respectively. The expressions of intercellular adhesion molecule-1 (ICAM-1) and matrix metalloproteinases-9(MMP-9) in PANC I cells were examined by immunocytochemistry before and after transfection. Results The migrational ability of PCNA I cells tr;ansfected with Ad-KAI1 was siginificantly decreased compared with untransfected PCNA I cells(P 〈 0.05). Immunocytochemistry study revealed that the expressions of ICAM-1 and MMP-9 were both positive in untransfected PCNA I cells, but were both negative in transfected PCNA I cells. Conclusion The inhibitory mechanism of KAI1 gene on metastasis of pancreatic cancer is associated with down-regulation of ICAM-1 and MMP-9 expressions.
关 键 词:胰腺肿瘤 Kangai-1蛋白 细胞粘附分子-1 金属蛋白酶-9
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