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E-selectin和ICAM-1在肝癌细胞与血管内皮细胞黏附作用中的实验研究 被引量:3

The effects of E-selectin and ICAM-1 on the adhesion of hepatocellular carcinoma cells and vascular endothelial cells
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摘要 目的探讨E-selectin(内皮细胞选择素)和ICAM-1(细胞间粘附分子-1)在肝癌细胞与血管内皮细胞黏附中的作用:筛选有临床应用前景、能预防肝癌复发与转移的抗黏附药物。方法实时荧光定量PCR检测E-selectin和ICAM-1mRNA在肝静脉内皮细胞ED25和脐静脉内皮TNFα刺激后细胞ECV304上的表达;应用体外粘附实验检测肝癌细胞HepG2与活化的ED25和ECV304的粘附,并检测不同药物对抗粘附作用的影响。结果 E-selectin和ICAM-1可高表达于活化后的ED25和ECV304;且能介导HepG2与ED25和ECV304的粘附;地塞米松、丹参酮ⅡA有较强的抑制HepG2与ED25粘附的作用。结论 E-selectin和ICAM-1可促进肝癌细胞与内皮细胞的粘附;地塞米松、丹参酮ⅡA可起到抗肝癌细胞与血管内皮细胞粘附的作用。 Objective To study the role of E-selectin and ICAM-1 on the adhesion of hepatocellular carcinoma cells and vascular endothelial cells,and to select related possible antiadhesion drugs to inhibit recurrence and metastasis of hepatocelluar carcinoma. Methods Expression of E-selectin and ICAM-1 in hepatic vein endothelial cells (ED25) and umbilical veinendothehal cells (ECV304)wcre detected by real-time quantitative PCR. Adhesion between the HepG2 cells and ED25 or ECV304 was examined by sohd phase adhesion assay in vitro. A number of drugs were tested for the affects on the tumor cell-endothelial adhesion. Results E-selectin and ICAM-1 were highly expressed on the surface of actived ED25 and ECV304, and could mediate the adhesion between HepG2 and ED25 or ECV304. Dexamethasone and tanshinone Ⅱ A were able to block the adhesion between HepG2 and ED25 at low concentration. Conclusion E-selectin and ICAM-1 are important moleculars on the adhesion of hepatoeellular carcinoma cells and endothelial cells. Dexamethasone and tanshinone Ⅱ A can be hopefully used as anti-adhesion drugs to inhibit the adhesion of hepatocellular carcinoma cells and vascular endothelial ceils.
出处 《岭南现代临床外科》 2009年第5期327-330,共4页 Lingnan Modern Clinics in Surgery
关键词 肝细胞癌 复发和转移 细胞粘附分子 HepatoceUular carcinoma Recurrence and metastasis Cellular adhesion molecule
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