期刊文献+

三聚β肽聚乙二醇化后抗肿瘤转移生物活性研究

Effect of the Pegylation of Trimeric β Peptide on It's Anti-metastasis Activity
原文传递
导出
摘要 目的:比较聚乙二醇(PEG)修饰对三聚β肽(β3)抗肿瘤转移活性的影响。方法:采用黏附试验观察β3及其PEG修饰物(β3-PEG)对肝癌细胞株与纤连蛋白(FN)黏附能力的影响;采用人工基底膜胶观察β3和β3-PEG对肿瘤细胞侵袭重组基底膜能力的影响。结果:β3和β3-PEG对肿瘤细胞SMMC-7721和HCCLM6与FN黏附能力均有显著的抑制作用(P<0.05),且呈剂量及时间正相关;PEG修饰可增强β3对2种肿瘤细胞的黏附抑制作用(P<0.05)。β3和β3-PEG对2种肿瘤细胞迁移和侵袭均有显著的抑制作用(P<0.05)。结论:PEG修饰可增强β3抗黏附作用,但对细胞迁移和侵袭的抑制作用无明显影响。 OBJECTIVE: To observe the effect of the polyglycol (PEG) modification of trimeric β peptide(β3) on it's anti - metastasis ability. METHODS: Using adhesion test to study the effects of β3 and β3- PEG on the adhesion of tumor cells to FN. Using artificial basal membrane to study the effects of β3 and β3- PEG on the invasion and recombination of basal membrane of tumor cells. RESULTS: Comparing to negative control, β3 and β3-PEG could both inhibit the adhesion of SMMC- 7721 and HCCLM6 tumor cells to FN with time- dependently(P〈 0.05) . The inhibitory effect of pegylated β3 peptide was stronger than that of β3 peptide(P 〈 0.05) . The mobility and invasion of HCCLM6 and SMMC- 7721 tumor cells were inhibited obviously by β3 and β3-PEG(P 〈 0.05). CONCLUSION: PEG modification could enhance the anti -adhesion effect of β3, but its inhibitory effect on the mobility and invasion of two kinds of tumor cells was not remarkable.
出处 《中国药房》 CAS CSCD 北大核心 2008年第13期970-972,共3页 China Pharmacy
基金 国家863计划(2001A215411,2004AA215201) 上海市现代生物与新药产业发展基金资助项目(024319212)
关键词 三聚β肽 聚乙二醇化 黏附分子 肿瘤细胞 Trimeric β peptide Pegylation Adhesive molecule Tumor cell
  • 相关文献

参考文献8

二级参考文献25

  • 1王松梅,朱珺,李岩,潘銮凤,查锡良,刘银坤.新型三聚β肽对人肝癌细胞系迁移和侵袭能力的影响[J].中华肝脏病杂志,2005,13(7):541-542. 被引量:2
  • 2[1]Zhou XD, Tang ZY, Yu YQ, et al. Recurrence after resection of alpha - fetoprotein positive hepatocellular carcinoma[J] .J Cancer Res Clin Oncol, 1994, 120:369 - 373.
  • 3[2]Tang ZY, Yu YQ, Zhou XD.An important approach in prolonging survival further after radical resection of AFP positive hepatocellular carcinoma [J] . J Exp Clin Cancer Res, 1984, 3:359 - 368.
  • 4[4]Sun FX, Tang ZY, Liu KD, et al. Establishment of a metastatic model of human hepatocellular carcinoma in nude mice via orthotopic implantation of histologically intact tissue[J] .Int J Cancer, 1996, 66:239 - 243.
  • 5[5]Tian J, Tang ZY, Ye SL, et al. New human hepatocellular carcinoma (HCC) cell line with highly metastatic potential (MHCC97) and its expression of the factors associated with metastasis[J]. Br J Cancer, 1999,81: 814 - 821.
  • 6[7]Sun J J, Zhou XD, Liu YK, et al. Inhibitory effects of synthetic β peptide on invasion and metastasis of liver cancer[ J ] . Cancer Res Clin Oncol, 2000, 126:595 - 600.
  • 7UEMURA T, NEMOTO A, LIU YK. Synthetic peptide derived from a conserved sequence of integrin β subunit [ J ]. Res Adv in Biosci & Bioeng, 2000,23( 1 ) :65-83.
  • 8VERONESE FM, SACCA B, POLVERINO de LAURETO P, et al.New PEGs for peptide and protein modification, suitable for identification of PEGylation site [J]. Bioconju Chem, 2001 ( 1 ) :62-70.
  • 9Okegawa Takatsugu,LY,Pong Reychen,et al.Cell adhesion proteins as tumor suppressors[J].Invest Urol,2002,167(4):1836-1843.
  • 10Liu YK,Nemoto A,Feng Y,et al.The binding ability to matrix proteins and the inhibitory effect on cell adhesion of synthetic peptides derived from a conserved sequence of integrins[J].J Biochem,1997;121(5):67-74.

共引文献32

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部