期刊文献+

肿瘤靶向多肽生物淘选技术研究进展 被引量:1

Advances in the research and development of phage display peptide library technology for biopanning of tumor targeting peptides
下载PDF
导出
摘要 生物淘选肿瘤或癌细胞的各种特异性靶向多肽是探索肿瘤早期诊断和治疗方法的有效途径.特异性靶向多肽既可用于探测肿瘤细胞表型特征,又可将其与抗癌药物结合进行靶向治疗,同时还可作为体内肿瘤的成像制剂,用于肿瘤及肿瘤细胞微转移的早期探测.噬菌体展示肽库技术能够有效地进行生物淘选或识别出与癌或肿瘤细胞某一靶点连结的,具有特异性、高亲和性的多肽.近年来,利用体内或体外噬菌体展示肽库技术已成功地淘选或识别出一些癌细胞的靶向多肽.本文就这些方面的研究进展进行了简要阐述,重点介绍了癌或肿瘤细胞靶向多肽的体外和体内生物淘选最新技术和临床应用. Bioparming tumor-specific or cancer-specific binding peptide as targeting factor is one of the effective methods for earlier diagnosis and treatment of tumor. Tumor-specific binding peptides can be used to probe the tumor cell surface phenotype and customize treatment accordingly by binding to an anticancer drug. Additionally, these targeting peptides can be used as in vivoimaging agents that allow for earlier detection of tumors and micrometastasis. Phage display is a powerful technique for the isolation of peptides that bind to a particular target with high affinity and specificity. The biopanning of intact cancer cells or tumors in animals can be used to isolate peptides that bind to cancer-specific cell surface biomarkers. Over the past 10 years, unbiased biopanning of phage-displayed peptide libraries has generated a suite of cancer targeting peptidic ligands. This review discusses the identification of surface features on cancer or tumor cells and methods of biopanning with phage display peptide technology in vitro and in vivo, and highlights advances in the research and development of screening of cancer or tumor cells targeting peptides as well as the use of the isolated peptides in clinical applications.
出处 《西南民族大学学报(自然科学版)》 CAS 2014年第3期358-363,共6页 Journal of Southwest Minzu University(Natural Science Edition)
关键词 靶向多肽 噬菌体展示肽库 体外(内)淘选 癌症细胞 肿瘤 phage display peptide library technology targeting peptide bioparming in vitro(in vivo) cancer cell tumor
  • 相关文献

参考文献29

  • 1LEWIS PHILIPS G,LI G,DUGGER D,et al.Trageting HER2-pstitive breast cancer with trastuzuman-DMl,an antibody-cytotoxic drug conjugate[J].Cancer Res,2008,68:9280-9290.
  • 2MEYERSON M,CARBONE DP.Genomie and proteomic profiling of lung cancers:Lung cancer classification in the age of targeted therapy[J].J Clin Oncol,2005,23:3219-3226.
  • 3CELIS JE,GROMOV P.Proteomics in translational cancer research:towards an integrated approach[J].Cancer Cell,2003,3:9-15.
  • 4Nielsen UB,Marks JD.Internalizing antibodies and targeted cancer therapy:direct selection from phage libraries[J].Pharm Sci Technol Today,2000,3:282-291.
  • 5ADAMS GP,WEINER LM.Monoclonal antibody therapy of cancer.Nat Biotechnol,2005,23:1147-1157.
  • 6BRAY BL.Large-scale manufacture of peptide therapeutics by chemical synthesis[J].Nat Rev Drug Discov,2003,2:587-593.
  • 7SCHALLY V,NAGY JA.New approaches to treatment of various cancers based on cytotoxic analogs of LHRH,somatosin,and bombesin[J].Life Sci,2003,72:2305-2320.
  • 8KEHOE J,KAY B.Filamentous phage display in the new millennium[J].Chem Rev,2005,105:4056-4072.
  • 9PASQUALINI R,RUOSLAHTI E.Organ targeting in vivo using phage display peptide libraries[J].Nature,1996,380:364-366.
  • 10BARRY MA,DOWER WJ,JOHNSTON SA.Toward cell-targeting gene therapy vectors:selection of cell-binding peptides from random peptide-presenting phage libraries[J].Nat Med,1996,2:299-305.

同被引文献2

引证文献1

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