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肿瘤血管靶向噬菌体展示肽的研究进展 被引量:3

Advances in the Research of Phage Display Peptides Targeting Tumor Vasculature
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摘要 肿瘤血管表达有正常血管内皮细胞没有或微量表达的蛋白,由于它们具有特征性的结构,故用噬菌体展示技术可以筛选出针对这些蛋白的特异性识别多肽。用此类肿瘤特异性识别多肽如RGD、NGR等作为抗肿瘤药物治疗的靶向分子,将其与药物、纳米颗粒或脂质体等结合起来,由此制备的纳米药物有望明显的抑制肿瘤的生长,并极大程度地减少化疗药物的毒副作用。除此之外,此类多肽还可用于肿瘤血管影像检测等领域的应用。 Tumor vascular endothelial cells can express some proteins which do not exist or express at a very low level in normal endothelial cells. The phage display peptide libraries can be employed to isolate some specific peptides targeting these proteins because of their distinctive structures. Peptides such as RGD, NGR, isolated by phage display and coupled with drugs and drug carriers such as nanoparticles, liposome, can enhance the efficacy of the therapy while reducing side effects of chemotherapeutics that are associated with traditional therapy. Additionally, such peptides can also be used for imaging and detection of tumor vasculature.
出处 《医学分子生物学杂志》 CAS CSCD 2006年第2期149-152,共4页 Journal of Medical Molecular Biology
基金 国家自然科学基金资助项目(No.30400185)~~
关键词 噬菌体展示 肿瘤治疗 血管内皮细胞 靶向肽 phage display tumor therapy vascular endothelial cells targeting peptide
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参考文献26

  • 1[1]JONES A,HARRIS A L.New developments in angiogenesis:a major mechanism for tumor growth and target for therapy[J].Cancer J Sci Am,1998,4(4):209-217. 被引量:1
  • 2[2]O' REILLY M S,PIRIE-SHEPHERD S,LANE W S,et al.Antiangiogenic activity of the cleaved conformation of the serpin antithrombin[J].Science,1999,285 (5 435):1926 -1928. 被引量:1
  • 3[3]SCOTT J K,SMITH G P.Searching for peptide ligands with an epitope library[.J].Science,1990,249(4967):386-390. 被引量:1
  • 4[4]PASQUALINI R,RUOSLAHTI E.Organ targeting in vivo using phage display peptide libraries[J].Nature,1996,380 (6572):364-366. 被引量:1
  • 5[5]HOFFMAN J A,GIRAUDO E,SINGH M,et al.Progressive vascular changes in a transgenic mouse model of squamous cell carcinoma[J].Cancer Cell,2003,4(5):383-391. 被引量:1
  • 6[6]JOYCE J A,LAAKKONEN P,BERNASCONI M,et al.Stagespecific vascular markers revealed by phage display in a mouse model of pancreatic islet tumorigenesis[J].Cancer Cell,2003,4(5):393-403. 被引量:1
  • 7[7]CHRISTIAN S,PILCH J,AKERMAN M E,et al.Nucleolin expressed at the cell surface is a marker of endothelial cells in angiogenic blood vessels[J].J Cell Biol,2003,163(4):871-878. 被引量:1
  • 8[8]KIM MY,BYEON,C W,HONG KH,et al.Inhibition of the angiogenesis by the MCP-1 (monocyte chemoattractant protein-1) binding peptide[J].FEBS Lett,2005,579 (7):1597 -1601. 被引量:1
  • 9[9]AN P,LEI H,ZHANG J,et al.Suppression of tumor growth and metastasis by a VEGFR-1 antagonizing peptide identified from a phage display library[J].Int J Cancer,2004,111 (2):165-173. 被引量:1
  • 10[10]ARAP W,PASQUALINI R,RUOSLAHTI E.Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model[J].Science,1998,279(5349):377-380. 被引量:1

同被引文献24

  • 1赵敏,陆江阳,吕艺.高迁移率族蛋白B1的生物学效应及在几种疾病发病中的作用[J].军事医学科学院院刊,2005,29(1):91-95. 被引量:12
  • 2郭莉,汤永民.噬菌体展示系统的研究进展[J].医学分子生物学杂志,2005,2(3):205-209. 被引量:4
  • 3张艳,何凤田,黎松,李蓉芬,钟小林,高会广,吉清,戴双双,陈麟凤,邢效如.人HMGB1 B Box的表达及其生物活性[J].中国生物化学与分子生物学报,2005,21(6):756-761. 被引量:3
  • 4ANDERSON U, WANG H, PALMBLAD K, et al. High mobility group 1 protein( HMG-1 )stimulates proinflammatory cytokine synthesis in human monocytes [ J ]. J Exp Med,2000,192 (4) : 565- 570. 被引量:1
  • 5CZURA C J,TRACEY K J. Targeting high mobility group box 1 as a late-acting mediator of inflammation [ J ]. Crit Care Med, 2003, 31 ( 1 ) : S46-50. 被引量:1
  • 6LI J,KOKKOLA R,TABIBZADEH S,et al. Structural basis for the pro-inflammatory cytokine activity of high mobility group box-1 [J]. Mol Med.2003.9(122) :3745. 被引量:1
  • 7BONALDI T, LANGST G, STROHNER R, et al. The DNA chaperone HMGB1 facilitates ACF/CHRAC-dependent nucleosome sliding[J]. EMBO J,2002,21 (24) :6865-6873. 被引量:1
  • 8LOTZE M T, DEMARCO R A. Dealing with death: HMGB1 as a novel target for cancer therapy [ J ]. Curr Opin Invest Drugs,2003, 4(12) :1405-1409. 被引量:1
  • 9ANDERSSON U,ERLANDSSON-Harris H. HMGBI is a potent trigger arthritis [ J ]. J Intern Med, 2004,255 ( 3 ) : 344 -350. 被引量:1
  • 10MAYROSE I, SHLOMI T, RUBINSTEIN N D,et al. Epitope mapping using combinatorial phage-display libraries:a graph-based algorithm[ J]. Nucleic Acids Res,2007,35 ( 1 ) :69-78. 被引量:1

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